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dc.contributor.authorZaitlen, Noah
dc.contributor.authorKraft, Peter
dc.date.accessioned2017-02-03T19:57:41Z
dc.date.available2017-02-03T19:57:41Z
dc.date.issued2012-07
dc.date.submitted2012-02
dc.identifier.issn0340-6717
dc.identifier.issn1432-1203
dc.identifier.urihttp://hdl.handle.net/1721.1/106855
dc.description.abstractHeritability, the fraction of phenotypic variation explained by genetic variation, has been estimated for many phenotypes in a range of populations, organisms, and time points. The recent development of efficient genotyping and sequencing technology has led researchers to attempt to identify the genetic variants responsible for the genetic component of phenotype directly via GWAS. The gap between the phenotypic variance explained by GWAS results and those estimated from classical heritability methods has been termed the “missing heritability problem”. In this work, we examine modern methods for estimating heritability, which use the genotype and sequence data directly. We discuss them in the context of classical heritability methods, the missing heritability problem, and describe their implications for understanding the genetic architecture of complex phenotypes.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (fellowship 5T32ES007142-27)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant R21 DK084529)en_US
dc.publisherSpringer-Verlagen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s00439-012-1199-6en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSpringer-Verlagen_US
dc.titleHeritability in the genome-wide association eraen_US
dc.typeArticleen_US
dc.identifier.citationZaitlen, Noah, and Peter Kraft. “Heritability in the Genome-Wide Association Era.” Human Genetics 131.10 (2012): 1655–1664.en_US
dc.contributor.departmentBroad Institute of MIT and Harvarden_US
dc.contributor.mitauthorKraft, Peter
dc.contributor.mitauthorZaitlen, Noah
dc.relation.journalHuman Geneticsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2016-08-18T15:27:20Z
dc.language.rfc3066en
dc.rights.holderSpringer-Verlag
dspace.orderedauthorsZaitlen, Noah; Kraft, Peteren_US
dspace.embargo.termsNen
mit.licensePUBLISHER_POLICYen_US


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