HGV2011: personalized genomic medicine meets the incidentalome.

Autor:	Wilson Sayres MA; Department of Statistics, University of California-Berkeley, Berkeley, California, USA. mwilsonsayres@berkeley.edu, Brookes AJ, Chanock SJ, Cheung VG, Goldstein DB, Jin L, Kwok PY
Jazyk:	angličtina
Zdroj:	Human mutation [Hum Mutat] 2012 Mar; Vol. 33 (3), pp. 582-5. Date of Electronic Publication: 2012 Jan 17.
DOI:	10.1002/humu.22008
Abstrakt:	The 12th International Meeting on Human Genome Variation and Complex Genome Analysis (HGV2011: Berkeley, California, USA, 8th-10th September 2011) was a stimulating workshop where researchers from academia and industry explored the latest progress, challenges, and opportunities in genome variation research. Key themes included progress beyond GWAS, variation in human populations, use of sequence data in medical settings, large-scale sequencing data analysis, and bioinformatics approaches to large datasets. (© 2011 Wiley-Liss, Inc.)
Databáze:	MEDLINE
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