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Thread | Thread Starter | Forum | Replies | Last Post |
CAGI -- Critical Assessment of Genome Interpretation 2013 | reece | Events / Conferences | 0 | 03-02-2013 05:28 PM |
help! samtools gave me more than 500,000 snps | slowsmile | Bioinformatics | 1 | 12-15-2011 09:24 AM |
building a cladogram with 100,000 sequences... | brachysclereid | Bioinformatics | 5 | 12-14-2011 07:07 AM |
Just published: "The $1,000 Genome" by Kevin Davies | natgenex | Events / Conferences | 9 | 10-01-2010 10:46 AM |
20,000 posts! | ECO | Site Announcements | 0 | 07-05-2010 07:12 PM |
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#1 |
Member
Location: Boston Join Date: Nov 2007
Posts: 11
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A full-length video of my talk at the NIH symposium to mark the 10th anniversary of the Human Genome Project has just been posted:
http://bit.ly/KDHGP10 This is a broad overview of the road to the $1,000 Genome, with observations on the Reference Genome, the state of next-gen sequencing, and the clinical impact of NGS. (I also have some fun at Francis Collins' expense...) Other speakers at the DNA Day symposium (April 25, 2013) included Collins, Ewan Birney (EBI), David Botstein (Princeton), Levi Garraway (HMS), and Sara Tishkoff (Penn). All videos are posted at the NHGRI's Genome TV channel on Youtube.
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Kevin Davies Author, The $1,000 Genome |
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#2 |
Junior Member
Location: the Netherlands Join Date: Mar 2013
Posts: 6
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Thanks for the upload, I thought it was a very informative talk!
Lots of things were mentioned that I had forgotten about, so it was nice to have my memory refreshed. Oof, a lot has happened in 10 years. Rather amazing when you think about where we are now. And I'm excited to know what more innovations we will see in the coming decade!
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-Proud to be a slightly stressed-out graduate intern. Also a: biologist, mycologist, botanist, palaeoecologist, typer-happy, and all-round nerd. |
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#3 |
Moderator
Cambridge, UK Community Forum Location: Cambridge, UK Join Date: Feb 2008
Posts: 221
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Time is on our side in running NGS experiments.
I just met with a user yesterday who wrote a grant 18 months ago to sequcne the exomes of 300 patients. Now he'd like to start. When the grant was written exomes cost 3 or 4 times as much to sequence. Many labs were still running single-capture reactions and Nextera capture was only an idea. Today we are looking at using the rapid exome and seqeuncing 6 samples per lane on HiSeq. If we actualy do the sequencing towards Christmas maybe Illumina's new flowcells wil be ready and we'll run 12 samples per lane on 2500. I conservativley sugested he up his sample numbers to 1000 and I think he can afford it! |
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#4 |
Junior Member
Location: the Netherlands Join Date: Mar 2013
Posts: 6
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Sequencing: yes. But what about the torrent of information that would produce? Who's to say his servers will be able to process 1000 exome sequences?
__________________
-Proud to be a slightly stressed-out graduate intern. Also a: biologist, mycologist, botanist, palaeoecologist, typer-happy, and all-round nerd. |
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Tags |
"$1000 genome", "human genome project", clinical genomics, illumina |
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