dc.contributor.author | Zaitlen, Noah | |
dc.contributor.author | Kraft, Peter | |
dc.date.accessioned | 2017-02-03T19:57:41Z | |
dc.date.available | 2017-02-03T19:57:41Z | |
dc.date.issued | 2012-07 | |
dc.date.submitted | 2012-02 | |
dc.identifier.issn | 0340-6717 | |
dc.identifier.issn | 1432-1203 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/106855 | |
dc.description.abstract | Heritability, 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.sponsorship | National Institutes of Health (U.S.) (fellowship 5T32ES007142-27) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (grant R21 DK084529) | en_US |
dc.publisher | Springer-Verlag | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1007/s00439-012-1199-6 | en_US |
dc.rights | Article 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.source | Springer-Verlag | en_US |
dc.title | Heritability in the genome-wide association era | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Zaitlen, Noah, and Peter Kraft. “Heritability in the Genome-Wide Association Era.” Human Genetics 131.10 (2012): 1655–1664. | en_US |
dc.contributor.department | Broad Institute of MIT and Harvard | en_US |
dc.contributor.mitauthor | Kraft, Peter | |
dc.contributor.mitauthor | Zaitlen, Noah | |
dc.relation.journal | Human Genetics | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2016-08-18T15:27:20Z | |
dc.language.rfc3066 | en | |
dc.rights.holder | Springer-Verlag | |
dspace.orderedauthors | Zaitlen, Noah; Kraft, Peter | en_US |
dspace.embargo.terms | N | en |
mit.license | PUBLISHER_POLICY | en_US |