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Article

Identification of genetic association of multiple rare variants using collapsing methods.

Genetic epidemiology - 1 Jan 2011

Sun Yan V, Sung Yun Ju, Tintle Nathan, Ziegler Andreas

Abstract excerpt

Next-generation sequencing technology allows investigation of both common and rare variants in humans. Exomes are sequenced on the population level or in families to further study the genetics of human diseases. Genetic Analysis Workshop 17 (GAW17) provided exomic data from the 1000 Genomes Project and simulated phenotypes. These data enabled evaluations of existing and newly developed statistical methods for...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22128049
DOI: 10.1002/gepi.20658
PMCID: PMC3289287

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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