--- Log opened Mon Feb 04 00:00:40 2019
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18:15 < justanotheruser> what is the best way to sequence dna? this looks interesting https://www.instructables.com/id/Arduino-PCR-thermal-cycler-for-under-85/
19:18 < jrayhawk> that depends on what you want it for
19:18 < jrayhawk> there are different levels of expense for different levels of accuracy and coverage
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21:05 < justanotheruser> jrayhawk: 1) self-testing DNA 2) knowledge about sequencing DNA
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22:02 < gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=38d88ad5 Bryan Bishop: transcript: threshold signatures >> http://diyhpl.us/diyhpluswiki/transcripts/sf-bitcoin-meetup/2019-02-04-threshold-signatures-and-accountability/
22:04 < gnusha> https://secure.diyhpl.us/cgit/diyhpluswiki/commit/?id=40341f0a Bryan Bishop: tweeter link >> http://diyhpl.us/diyhpluswiki/transcripts/sf-bitcoin-meetup/2019-02-04-threshold-signatures-and-accountability/
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22:47 < nmz787> justanotheruser: most likely using a PCR thermocycler as a lead-in to sequencing is targeting small chunks (few hundred basepairs), particularly via a process called
22:47 < nmz787> .wik sanger sequencing
22:47 < yoleaux> "Sanger sequencing is a method of DNA sequencing first commercialized by Applied Biosystems, based on the selective incorporation of chain-terminating dideoxynucleotides by DNA polymerase during in vitro DNA replication. Developed by Frederick Sanger and colleagues in 1977, it was the most widely used sequencing method for approximately 40 years." — https://en.wikipedia.org/wiki/Sanger_sequencing
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--- Log closed Tue Feb 05 00:00:40 2019