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	<id>https://ssi-wiki.stanford.edu/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Rfuisz</id>
	<title>Stanford SSI Wiki - User contributions [en]</title>
	<link rel="self" type="application/atom+xml" href="https://ssi-wiki.stanford.edu/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Rfuisz"/>
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	<updated>2026-05-31T06:13:35Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2330</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2330"/>
		<updated>2016-12-02T20:28:09Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Biology STARS Training on Axess */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit a PDF of your STARS training to [http://internal.stanfordssi.org/trainings internal site], making sure that your name can be seen in the screenshot.&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete the [https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form], read the [https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy], and complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads). Once confirmed on our side, you should be cleared for access.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2255</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2255"/>
		<updated>2016-10-20T18:48:07Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit a PDF of your STARS training to [http://internal.stanfordssi.org/trainings internal site], making sure to include your name somewhere in the screenshot.&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete the [https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form], read the [https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy], and complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads). Once confirmed on our side, you should be cleared for access.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2254</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2254"/>
		<updated>2016-10-20T18:47:05Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete the [https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form], read the [https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy], and complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads).&lt;br /&gt;
&lt;br /&gt;
Once you have completed the form, training, and orientation, submit your PDF form and proof of completion of your STARS training through the [http://internal.stanfordssi.org/trainings internal site]. Once confirmed on our side, you should be cleared for access.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2253</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2253"/>
		<updated>2016-10-20T18:46:29Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete the [https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]. Read the [https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads).&lt;br /&gt;
&lt;br /&gt;
Once you have completed the form, training, and orientation, submit your PDF form and proof of completion of your STARS training through the [http://internal.stanfordssi.org/trainings internal site]. Once confirmed on our side, you should be cleared for access.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2252</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2252"/>
		<updated>2016-10-20T18:46:06Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete the [https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads).&lt;br /&gt;
&lt;br /&gt;
Once you have completed the form, training, and orientation, submit your PDF form and proof of completion of your STARS training through the [http://internal.stanfordssi.org/trainings internal site]. Once confirmed on our side, you should be cleared for access.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2251</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2251"/>
		<updated>2016-10-18T22:55:59Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space. For information on how to join the project, join the SSI Slack and go to the #biology channel, and read information on how to get [[Wet Lab Access]] on this wiki.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
&lt;br /&gt;
DNA synthesis is currently done using the [https://en.wikipedia.org/wiki/Oligonucleotide_synthesis#Synthetic_cycle phosphoramidite method]. However, phosphoramidite chemistry produced large volumes of hazardous waste, requires precise chemical conditions, and is limited to producing short strands of DNA (oligonucleotides) on the order of ~100 basepairs. Most genes of interest are in the ~5,000 basepair range, so current synthesis methods cannot create a gene-length piece of DNA without further processing. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ TdT is one possible enzyme to consider,] and has previously been [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf the subject of some prior theoretical work.]&lt;br /&gt;
&lt;br /&gt;
Enzymatic DNA synthesis would be a great alternative way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency of synthesizing DNA in space. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. Similar oligonucleotide synthesizers that don&#039;t quite fit our needs [[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 have been made in the past,] although our final design will most likely look different. Good things to know about when designing a device like this: [https://en.wikipedia.org/wiki/Diaphragm_pump diaphragm pumps], [https://en.wikipedia.org/wiki/Solenoid_valve solenoid valves], and of course [https://en.wikipedia.org/wiki/Microfluidics microfluidics in general].&lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
Our chemistry may look something like [https://en.wikipedia.org/wiki/Polymerase_cycling_assembly Polymerase Chain Assembly, also called Assembly PCR].&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2250</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2250"/>
		<updated>2016-10-18T18:28:41Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* SSI Bio 2016 Pilot Project */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space. For information on how to join the project, join the SSI Slack and go to the #biology channel, and read information on how to get [[Wet Lab Access]] on this wiki.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
&lt;br /&gt;
DNA synthesis is currently done using the [https://en.wikipedia.org/wiki/Oligonucleotide_synthesis#Synthetic_cycle phosphoramidite method]. However, phosphoramidite chemistry produced large volumes of hazardous waste, requires precise chemical conditions, and is limited to producing short strands of DNA (oligonucleotides) on the order of ~100 basepairs. Most genes of interest are in the ~5,000 basepair range, so current synthesis methods cannot create a gene-length piece of DNA without further processing.&lt;br /&gt;
&lt;br /&gt;
Enzymatic DNA synthesis would be a great alternative way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency of synthesizing DNA in space. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. Good things to know about when designing a device like this: [https://en.wikipedia.org/wiki/Diaphragm_pump diaphragm pumps], [https://en.wikipedia.org/wiki/Solenoid_valve solenoid valves], and of course [https://en.wikipedia.org/wiki/Microfluidics microfluidics in general].&lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
Our chemistry may look something like [https://en.wikipedia.org/wiki/Polymerase_cycling_assembly Polymerase Chain Assembly, also called Assembly PCR].&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2249</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2249"/>
		<updated>2016-10-18T18:27:19Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Lab Safety Forms &amp;amp; Orientation */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads).&lt;br /&gt;
&lt;br /&gt;
Once you have completed the forms, training, and orientation, submit your PDF form and proof of completion of your STARS training through the [http://internal.stanfordssi.org/trainings internal site]. Once confirmed on our side, you should be cleared for access.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2248</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2248"/>
		<updated>2016-10-18T18:27:00Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;br /&gt;
&lt;br /&gt;
Once you have completed the forms, training, and orientation, submit your PDF form and proof of completion of your STARS training through the [http://internal.stanfordssi.org/trainings internal site]. Once confirmed on our side, you should be cleared for access.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2247</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2247"/>
		<updated>2016-10-18T18:24:45Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2246</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2246"/>
		<updated>2016-10-18T18:24:31Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* SSI Membership */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Orientation&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]]. Once you&#039;ve joined SSI, read on!&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2245</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2245"/>
		<updated>2016-10-18T18:24:13Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* SSI Membership */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Orientation&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
In order to get clearance for the Bio team wetlab space, you also need to have SSI membership and do the usual process as well. Check out: [[How to Join SSI]].&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2244</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2244"/>
		<updated>2016-10-18T18:14:58Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Enzymatic Synthesis Chemistry */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
&lt;br /&gt;
DNA synthesis is currently done using the [https://en.wikipedia.org/wiki/Oligonucleotide_synthesis#Synthetic_cycle phosphoramidite method]. However, phosphoramidite chemistry produced large volumes of hazardous waste, requires precise chemical conditions, and is limited to producing short strands of DNA (oligonucleotides) on the order of ~100 basepairs. Most genes of interest are in the ~5,000 basepair range, so current synthesis methods cannot create a gene-length piece of DNA without further processing.&lt;br /&gt;
&lt;br /&gt;
Enzymatic DNA synthesis would be a great alternative way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency of synthesizing DNA in space. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. Good things to know about when designing a device like this: [https://en.wikipedia.org/wiki/Diaphragm_pump diaphragm pumps], [https://en.wikipedia.org/wiki/Solenoid_valve solenoid valves], and of course [https://en.wikipedia.org/wiki/Microfluidics microfluidics in general].&lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
Our chemistry may look something like [https://en.wikipedia.org/wiki/Polymerase_cycling_assembly Polymerase Chain Assembly, also called Assembly PCR].&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2243</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2243"/>
		<updated>2016-10-18T18:11:59Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Microfluidic Synthesizer Design */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency of synthesizing DNA in space. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. Good things to know about when designing a device like this: [https://en.wikipedia.org/wiki/Diaphragm_pump diaphragm pumps], [https://en.wikipedia.org/wiki/Solenoid_valve solenoid valves], and of course [https://en.wikipedia.org/wiki/Microfluidics microfluidics in general].&lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
Our chemistry may look something like [https://en.wikipedia.org/wiki/Polymerase_cycling_assembly Polymerase Chain Assembly, also called Assembly PCR].&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2242</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2242"/>
		<updated>2016-10-18T18:07:18Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Reassembly Chemistry and Algorithm */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency of synthesizing DNA in space. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
Our chemistry may look something like [https://en.wikipedia.org/wiki/Polymerase_cycling_assembly Polymerase Chain Assembly, also called Assembly PCR].&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2241</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2241"/>
		<updated>2016-10-18T18:07:05Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Reassembly Chemistry and Algorithm */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency of synthesizing DNA in space. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
Our chemistry can look something like [https://en.wikipedia.org/wiki/Polymerase_cycling_assembly Polymerase Chain Assembly, also called Assembly PCR].&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2240</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2240"/>
		<updated>2016-10-18T18:03:48Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Improved Speed and Efficiency */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency of synthesizing DNA in space. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2239</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2239"/>
		<updated>2016-10-18T18:01:16Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Inspiration and Research */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA Synthesizer Idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2238</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2238"/>
		<updated>2016-10-18T18:01:05Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Payload Size and Power constraints */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power Constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2237</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2237"/>
		<updated>2016-10-18T18:00:50Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Improved speed and efficiency */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved Speed and Efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2236</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2236"/>
		<updated>2016-10-18T18:00:38Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Recyclability, creation on site */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, On-Site Reagent Synthesis====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself.&lt;br /&gt;
&lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2235</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2235"/>
		<updated>2016-10-18T18:00:13Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Communication from Device */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
===Communication from Device===&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2234</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2234"/>
		<updated>2016-10-18T18:00:01Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* What kind of shielding do we need? */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===Shielding Requirements===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2233</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2233"/>
		<updated>2016-10-18T17:59:35Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching 2016 by sending a DNA synthesizer into space.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2232</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2232"/>
		<updated>2016-10-18T17:58:05Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Orientation&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
[[How to Join SSI]]&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Orientation==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Orientation - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2231</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2231"/>
		<updated>2016-10-18T17:57:41Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Walkthrough&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
[[How to Join SSI]]&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Walkthrough==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And complete a Lab Safety Walkthrough - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2230</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2230"/>
		<updated>2016-10-18T17:57:15Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Walkthrough&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
[[How to Join SSI]]&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Walkthrough==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And read this: &lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Complete a Lab Safety Walkthrough - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2229</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2229"/>
		<updated>2016-10-18T17:56:54Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Walkthrough&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
[[How to Join SSI]]&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Walkthrough==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And read this: &lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Complete a Lab Safety Walkthrough - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2228</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2228"/>
		<updated>2016-10-18T17:56:40Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Walkthrough&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
[[How to Join SSI]]&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site]].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Walkthrough==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And read this: &lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Complete a Lab Safety Walkthrough - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2227</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2227"/>
		<updated>2016-10-18T17:56:22Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Walkthrough&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
[[How to Join SSI]]&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site]].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Forms &amp;amp; Walkthrough==&lt;br /&gt;
Complete these two forms:&lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/sites/default/files/student_project-club_agreement_form_20160913.pdf Student Project Form]&lt;br /&gt;
[https://docs.google.com/forms/d/e/1FAIpQLSfDBxh1TUQi2VV9coo2dgnhOWqFKCKgvP6GhXFxkbw3mWG1jw/viewform?c=0&amp;amp;w=1 Student Safety Form]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
And read this: &lt;br /&gt;
[https://uytengsuteachinglab.stanford.edu/uytengsu-teaching-lab-policy#Student%20Club Wet Lab Policy]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Complete a Lab Safety Walkthrough - discussed on SSI&#039;s Slack (or contact Bio Team Co-Leads)&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2226</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2226"/>
		<updated>2016-10-17T07:06:28Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Sources of Inspiration and Research */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=User:Rfuisz&amp;diff=2225</id>
		<title>User:Rfuisz</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=User:Rfuisz&amp;diff=2225"/>
		<updated>2016-10-17T07:05:12Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: Created page with &amp;quot;Richard Fuisz is a Co-Lead for SSI Biology. Richard is a senior in bioengineering.&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Richard Fuisz is a Co-Lead for SSI Biology. Richard is a senior in bioengineering.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2224</id>
		<title>Biology Team</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2224"/>
		<updated>2016-10-17T07:04:20Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
Biology team was officially started in Fall 2016. Active Team Leads are Richard Fuisz and Alan Tomusiak.&lt;br /&gt;
&lt;br /&gt;
==Joining Bio Team==&lt;br /&gt;
Check out [[Wet Lab Access]] for instructions on how to get cleared for access to our lab space.&lt;br /&gt;
&lt;br /&gt;
==Our Projects==&lt;br /&gt;
We&#039;re currently building the world&#039;s first [[DNA Synthesizer]] to make DNA in space. Come join us!&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2223</id>
		<title>Biology Team</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2223"/>
		<updated>2016-10-17T07:04:10Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
Biology team was officially started in Fall 2016. &lt;br /&gt;
&lt;br /&gt;
Active Team Leads are Richard Fuisz and Alan Tomusiak.&lt;br /&gt;
&lt;br /&gt;
==Joining Bio Team==&lt;br /&gt;
Check out [[Wet Lab Access]] for instructions on how to get cleared for access to our lab space.&lt;br /&gt;
&lt;br /&gt;
==Our Projects==&lt;br /&gt;
We&#039;re currently building the world&#039;s first [[DNA Synthesizer]] to make DNA in space. Come join us!&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2222</id>
		<title>Biology Team</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2222"/>
		<updated>2016-10-17T07:02:29Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Active Team Leads are Richard Fuisz and Alan Tomusiak.&lt;br /&gt;
&lt;br /&gt;
==Joining Bio Team==&lt;br /&gt;
Check out [[Wet Lab Access]] for instructions on how to get cleared for access to our lab space.&lt;br /&gt;
&lt;br /&gt;
==Our Projects==&lt;br /&gt;
We&#039;re currently building the world&#039;s first [[DNA Synthesizer]] to make DNA in space. Come join us!&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2221</id>
		<title>Biology Team</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2221"/>
		<updated>2016-10-17T07:01:44Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
==Joining Bio Team==&lt;br /&gt;
Check out [[Wet Lab Access]] for instructions on how to get cleared for access to our lab space.&lt;br /&gt;
&lt;br /&gt;
==Our Projects==&lt;br /&gt;
We&#039;re currently building the world&#039;s first [[DNA Synthesizer]] to make DNA in space. Come join us!&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_synthesizer&amp;diff=2220</id>
		<title>DNA synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_synthesizer&amp;diff=2220"/>
		<updated>2016-10-17T07:01:26Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: Rfuisz moved page DNA synthesizer to DNA Synthesizer&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;#REDIRECT [[DNA Synthesizer]]&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2219</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2219"/>
		<updated>2016-10-17T07:01:26Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: Rfuisz moved page DNA synthesizer to DNA Synthesizer&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Sources of Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2218</id>
		<title>Biology Team</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2218"/>
		<updated>2016-10-17T07:00:56Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{biology-stub}}&lt;br /&gt;
&lt;br /&gt;
==Joining Bio Team==&lt;br /&gt;
Check out [[Wet Lab Access]] for instructions on how to get cleared for access to our lab space.&lt;br /&gt;
&lt;br /&gt;
==Our Projects==&lt;br /&gt;
We&#039;re currently building the world&#039;s first [[DNA Synthesizer]] to make DNA in space. Come join us!&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2217</id>
		<title>Biology Team</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Biology_Team&amp;diff=2217"/>
		<updated>2016-10-17T07:00:12Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{biology-stub}}&lt;br /&gt;
&lt;br /&gt;
==Joining Bio Team==&lt;br /&gt;
Check out [Wet Lab Access] for instructions on how to get cleared for access to our lab space.&lt;br /&gt;
&lt;br /&gt;
==Our Projects==&lt;br /&gt;
We&#039;re currently building the world&#039;s first [DNA Synthesizer] to make DNA in space. Come join us!&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2216</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2216"/>
		<updated>2016-10-17T06:57:56Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* Sources of Inspiration and Research */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Sources of Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2215</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2215"/>
		<updated>2016-10-17T06:57:40Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==Sources of Inspiration and Research==&lt;br /&gt;
[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 This paper describes a compact microfluidic DNA synthesizer, as well as an integrated &amp;quot;verifier&amp;quot; device to ensure that the correct sequence was synthesized.]&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735642/pdf/11693_2009_Article_9023.pdf This paper describes a theoretical strategy for using TdT to perform enzymatic DNA synthesis.]&lt;br /&gt;
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846215/ This paper gets deeper into TdT and how it functions in a more natural context.]&lt;br /&gt;
&lt;br /&gt;
===History of DNA synthesizer idea in SSI===&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2214</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2214"/>
		<updated>2016-10-17T06:47:16Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: /* DNA Product Verification */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==History of DNA synthesizer idea in SSI==&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2213</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2213"/>
		<updated>2016-10-17T06:47:00Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle each critical component of the synthesizer.&lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence. [[http://scholarbank.nus.edu.sg/bitstream/handle/10635/20904/WangC.pdf?sequence=1 One possible strategy comes from this paper]] - essentially tagging oligo and looking for fluoresence as a sign that homology was sufficiently similar to produce a result.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
===Physical Stress of Launch===&lt;br /&gt;
Similar to any other payload, our DNA synthesizer will have to be durable enough to withstand the stresses and forces associated with launch.&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==History of DNA synthesizer idea in SSI==&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2212</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2212"/>
		<updated>2016-10-17T06:43:08Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project: A DNA Synthesizer for Space.&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle the several different systems needed &lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==History of DNA synthesizer idea in SSI==&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2211</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2211"/>
		<updated>2016-10-17T06:42:53Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
Biology Team&#039;s Pilot Project&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle the several different systems needed &lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==History of DNA synthesizer idea in SSI==&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2210</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2210"/>
		<updated>2016-10-17T06:42:44Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{{biology-stub}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Biology Team&#039;s Pilot Project&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle the several different systems needed &lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==History of DNA synthesizer idea in SSI==&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2209</id>
		<title>DNA Synthesizer</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=DNA_Synthesizer&amp;diff=2209"/>
		<updated>2016-10-17T06:42:25Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
{Stub-Biology}&lt;br /&gt;
&lt;br /&gt;
Biology Team&#039;s Pilot Project&lt;br /&gt;
&lt;br /&gt;
==SSI Bio 2016 Pilot Project==&lt;br /&gt;
SSI Bio is launching with the DNA synthesizer as their primary project.&lt;br /&gt;
&lt;br /&gt;
==Components of the Synthesis Project==&lt;br /&gt;
SSI Bio will be breaking up this DNA synthesizer project into several smaller subteams to tackle the several different systems needed &lt;br /&gt;
&lt;br /&gt;
===Enzymatic Synthesis Chemistry===&lt;br /&gt;
Enzymatic DNA synthesis would be a great way to synthesize DNA in space, for the following reasons:&lt;br /&gt;
====Safety, Non-flammability, Non-toxicity====&lt;br /&gt;
Most enzymatic reagents could in theory be aqueous solutions, unlike the acetonitrile organic solvents typically used in phosphoramidite chemistry.&lt;br /&gt;
====Recyclability, creation on site====&lt;br /&gt;
If most of the reagents used are enzymes, then in theory these enzymes could be made by bacteria and then purified on site. This might mean that reagents could be produced, and modified, by the machine itself. &lt;br /&gt;
====Improved speed and efficiency====&lt;br /&gt;
It may be possible that an enzymatic method could improve the speed and efficiency with which this reaction takes place. This would be split into two effects. First, being able to make longer strands of DNA (oligonucleotides) would mean that the final product could be composed of fewer parts, which makes the creation of algorithms and strategies for reassembling this DNA to become much easier. Second, being able to make longer strands of DNA faster would cut down substantially on the complexity and time involved with synthesizing DNA.&lt;br /&gt;
&lt;br /&gt;
===Safe Phosphoramidite Chemistry===&lt;br /&gt;
A more conventional alternative to aiming for enzymatic synthesis would be to try to adjust conventional phosphoramidite chemistry to be safer for use in space. This might involve creating a system that can synthesize DNA using safer organic solvents and less toxic reagents.&lt;br /&gt;
&lt;br /&gt;
===Microfluidic Synthesizer Design===&lt;br /&gt;
To fit all of these fluidic parts into a small enough payload, we have to make everything quite small. Microfluidics is a good way to do this. &lt;br /&gt;
&lt;br /&gt;
===Reassembly Chemistry and Algorithm===&lt;br /&gt;
&lt;br /&gt;
===DNA Product Verification===&lt;br /&gt;
&lt;br /&gt;
Once a strand of DNA is made, we will need to check to make sure that it is the correct desired sequence.&lt;br /&gt;
&lt;br /&gt;
==Effects of Space on Synthesizer==&lt;br /&gt;
&lt;br /&gt;
===Payload Size and Power constraints===&lt;br /&gt;
We&#039;d like to fit our synthesizer into a 10 centimeter cube, so that it could be launched on a [https://en.wikipedia.org/wiki/CubeSat CubeSat] or another standardized research payload.&lt;br /&gt;
&lt;br /&gt;
===What kind of shielding do we need?===&lt;br /&gt;
We&#039;re not sure what kind of shielding we need! UV radiation can have damage DNA through a process called [https://en.wikipedia.org/wiki/Direct_DNA_damage Direct DNA damage] that can lead to thymine or pyrimidine dimers. This is what causes sunburn, and it&#039;s why your skin can tan to help block out UVB.&lt;br /&gt;
&lt;br /&gt;
====Communication from Device====&lt;br /&gt;
Depending on our strategy for launching to space, communication from our device to some sort of receiver we can listen to involves a number of interesting questions. How do we return the message that synthesis has been carried out successfully? Will the message describe the sequence of the product created, or a simple boolean yes or no?&lt;br /&gt;
&lt;br /&gt;
==History of DNA synthesizer idea in SSI==&lt;br /&gt;
The idea of a DNA synthesizer for space has been floating around SSI for some time. [[John Cumbers - Synthetic Biology | One of the earliest recordings stretches back to 2013, in a talk given John Cumbers.]] John Cumbers was also consulted during the initial conception and planning of the project in the summer of 2015.&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2208</id>
		<title>Wet Lab Access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_Lab_Access&amp;diff=2208"/>
		<updated>2016-10-17T06:41:25Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category:Biology]]&lt;br /&gt;
&lt;br /&gt;
SSI Bio&#039;s wetlab access procedures!&lt;br /&gt;
&lt;br /&gt;
You need 4 things to get wetlab access: SSI Membership, STARS training, Uytengensu Lab access forms, and a Lab Safety Walkthrough&lt;br /&gt;
&lt;br /&gt;
==SSI Membership==&lt;br /&gt;
[[How to Join SSI]]&lt;br /&gt;
&lt;br /&gt;
==Biology STARS Training on Axess==&lt;br /&gt;
In addition to your STARS trainings for SSI General Membership, you will also need to do:&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1500 Biosafety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EHS-1600 Bloodborne Pathogens&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Submit screenshots proving your completion those through the [http://internal.stanfordssi.org/trainings internal site]].&lt;br /&gt;
&lt;br /&gt;
==Lab Safety Walthrough==&lt;br /&gt;
We&#039;ll be providing more information on this as we start to get into lab. Stay tuned!&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
	<entry>
		<id>https://ssi-wiki.stanford.edu/w/index.php?title=Wet_lab_access&amp;diff=2207</id>
		<title>Wet lab access</title>
		<link rel="alternate" type="text/html" href="https://ssi-wiki.stanford.edu/w/index.php?title=Wet_lab_access&amp;diff=2207"/>
		<updated>2016-10-17T06:41:08Z</updated>

		<summary type="html">&lt;p&gt;Rfuisz: Rfuisz moved page Wet lab access to Wet Lab Access&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;#REDIRECT [[Wet Lab Access]]&lt;/div&gt;</summary>
		<author><name>Rfuisz</name></author>
	</entry>
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