How next-gen sequencing changes the work of a small biology lab
David Roy Smith in the current Frontiers in Genetics has an opinion article that reflects on the way that next-generation sequencing technologies have change...
David Roy Smith in the current Frontiers in Genetics has an opinion article that reflects on the way that next-generation sequencing technologies have change...
MIT Technology Review has an article this week about Razib Khan’s efforts to sequence his baby son in utero: “For One Baby, Life Begins with Genome Revealed”.
A new paper by Meredith Carpenter and colleagues describes a novel method that can greatly enrich the yield of DNA from ancient samples:
Sequencing bacterial genomes is now the scope of project routinely undertaken by undergraduates just learning how to do research. What was once an empirical ...
From the Guardian, a pause to consider how ordinary complete genome analysis has become: “Genome research: discovery as an everyday event”.
Today, Svante Pääbo’s group at the Max Planck Institute for Evolutionary Anthropology released high-coverage sequence data from a toe bone from Denisova Cave...
Misha Angrist, writing in Nature News comments (“Genetic privacy needs a more nuanced approach”) on the recent study that demonstrated the possibility of fin...
Jay Shendure and Erez Lieberman Aiden have a recent review in Nature Biotechnology that provides some recent data on the falling cost and increased use of ge...
Razib Khan comments on 23andMe’s pursuit of FDA clearance for their genome service:
Alon Keinan and Andrew Clark have a short report in the current Science examining the effects of recent human population growth on the expected spectrum of h...
John Lauerman reports in BusinessWeek on his experience participating in the Personal Genome Project:
Holly Dunsworth, at the University of Rhode Island, is undertaking a unique project with her undergraduate course this semester, providing 23andMe genotyping...
Of some interest with respect to DNA databases and privacy concerns: “DNA links 1991 killing to Colonial-era family”.
The New York Times notices DNA sequencing’s Malthusian trap: “DNA sequencing caught in deluge of data.”
The Archon Genomics X Prize is a $10 million contest to see what company or organization can develop a low-cost accurate sequencing technology. The AP’s Malc...
The new Genome Biology has a perspective piece by Jacob Tennessen and colleagues, titled “The promise and limitations of population exomics for human evoluti...
Joe Pickrell encountered sticker shock when faced with the prospect of a medical sequencing test: “The week that I worried I had a rare genetic disease”.
Misha Angrist turns on the sarcasm filter for a proposal to discard raw data that may trouble research subjects (“If you want to destroy my sweater”):
Matthew Herper is a science and medicine contributing writer at Forbes.com. He has just written a series of posts themed as “Gene Week”, focusing on advances...
The first of the papers describing results from the 1000 Genomes project has been released today in Nature 1000Genomes:Nature:2010.
Last week, a paper looking for the genetic causes of Miller syndrome reported the whole genomes of four members of a single family: two siblings with the dis...
Remember Genome 10K? Well, here’s a new study by Michel Milinkovitch and colleagues, that points out the deficiencies of comparative data from 1X genomes:
Daniel MacArthur reports from the Advances in Genome Biology and Technology meetings are full of little snippets of next-generation sequencing news; good if ...
John Timmer gives a great summary of the new paper in Science covering the Complete Genomics sequencing method.
IBM joins the next-gen sequencing race:
Software publisher O’Reilly is running an interview with David Dooling, data chief of the Genome Sequencing Center at Washington University: “Sequencing a ge...
In yesterday’s NY Times: