![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
AGBT 2013 posters | swarner | Events / Conferences | 0 | 02-26-2013 11:09 AM |
Agbt 2013 | paulk | Events / Conferences | 0 | 02-16-2013 08:01 AM |
'Spring School 2013 - Epigenetics of Civilization Diseases', May 27th - 31st 2013 | ecSeq Bioinformatics | Events / Conferences | 1 | 01-31-2013 02:17 PM |
Have a great 2013! | EricP | Introductions | 0 | 01-09-2013 03:03 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Registered Vendor
Location: genohub.com Join Date: Mar 2013
Posts: 210
|
![]()
Day 1 highlights of Sequencing, Finishing and Analysis in the Future Meeting (SFAF 2013)
• All four platforms are actively trying to increase their read lengths (although we didn’t see significant guidance beyond Ion’s 400 bp reads) • Haley mentioned that Illumina’s latest aquisition of Moleculo technology might one day replace current Mate-pair library prep (if prices can be lowered). • MiSeq DX was pulled back because Illumina has been able to increase MiSeq output. A clinical instrument will require a locked down platform. • Turner said that he expects 30,000 PacBio base pairs in 3 years. Shearing technologies and polymerases would have to be improved for better-read lengths. • PGM can produce >2G aligned Q20 bases with even coverage (E. coli) using their 318, 400 bp chip. • Fiske said that Illumina spends 25% of revenue on R&D, Life Tech and Thermo spend 5% and 3% respectively. • Illumina needs help with better and higher fidelity polymerases. Suggested that Illumina would consider purchasing companies who have breakthrough technologies related to polymerases. SFAF day 1 summary Last edited by Genohub; 07-29-2013 at 03:16 PM. Reason: link update |
![]() |
![]() |
![]() |
Tags |
sfaf, sfaf 2013 |
Thread Tools | |
|
|