martes, 25 de septiembre de 2012

Implicating Sequence Variants in Human Disease

Implicating Sequence Variants in Human Disease

Genome.gov National Human Genome Research Institute National Institutes of Health


 

Implicating Sequence Variants in Human Disease


Live Stream Image of Implicating Sequence Variants in Human Disease meeting
On September 12-13, 2012, the National Human Genome Research Institute (NHGRI), sponsored a workshop — Implicating Sequence Variants in Human Disease — at the Hyatt Regency Bethesda, in Bethesda, Md. Teri Manolio, M.D., Ph.D., NHGRI, and Daniel MacArthur, Ph.D., Massachusetts General Hospital, co-chaired the workshop. The goal of the workshop was to develop guidelines for investigators, reviewers and editors to consider in assessing the evidence implicating sequence variants or genes as causal in a specific disease.
Videos and some accompanying slides from the workshop

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