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dc.contributor.authorGrossman, Sharon Rachel
dc.contributor.authorKarlsson, Elinor K.
dc.contributor.authorTabrizi, Shervin
dc.contributor.authorAndersen, Kristian G.
dc.contributor.authorRinn, John L.
dc.contributor.authorLander, Eric S.
dc.contributor.authorSchaffner, Steve
dc.contributor.authorSabeti, Pardis C.
dc.contributor.author1000 Genomes Project Consortium
dc.contributor.authorShlyakhter, Ilya, 1975-
dc.date.accessioned2012-04-05T18:33:17Z
dc.date.available2012-04-05T18:33:17Z
dc.date.issued2010-10
dc.identifier.issn1465-6906
dc.identifier.issn1474-7596
dc.identifier.urihttp://hdl.handle.net/1721.1/69960
dc.description.abstractThe human genome contains hundreds of regions in which the patterns of genetic variation indicate recent positive natural selection, yet for most of these the underlying gene and the advantageous mutation remain unknown. We recently reported the development of a method, Composite of Multiple Signals (CMS), that combines tests for multiple signals of natural selection and increases resolution by up to 100-fold.en_US
dc.language.isoen_US
dc.publisherBioMed Central Ltd.en_US
dc.relation.isversionofhttp://genomebiology.com/2010/11/S1/I22en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Centralen_US
dc.titleMining data from 1000 genomes to identify the causal variant in regions under positive selectionen_US
dc.typeArticleen_US
dc.identifier.citationGrossman, Shari et al. "Mining data from 1000 genomes to identify the causal variant in regions under positive selection." Genome Biology 2010, 11(Suppl 1):I22 (11 October 2010).en_US
dc.contributor.departmentWhitaker College of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.approverLander, Eric S.
dc.contributor.mitauthorGrossman, Sharon Rachel
dc.contributor.mitauthorShlyakhter, Ilya
dc.contributor.mitauthorKarlsson, Elinor K.
dc.contributor.mitauthorTabrizi, Shervin
dc.contributor.mitauthorAndersen, Kristian
dc.contributor.mitauthorRinn, John L.
dc.contributor.mitauthorLander, Eric S.
dc.contributor.mitauthorSchaffner, Steve
dc.contributor.mitauthorSabeti, Pardis C.
dc.relation.journalGenome Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsGrossman, Shari; Shlyakhter, Ilya; Karlsson, Elinor K.; Tabrizi, Shervin; Andersen, Kristian; Rinn, John; Lander, Eric; Schaffner, Steve; Sabeti, Pardis C.; The 1000 Genomes Projecten_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5410-7274
dspace.mitauthor.errortrue
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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