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Association screening for genes with multiple potentially rare variants: an inverse-probability weighted clustering approach

Both common variants and rare variants are involved in the etiology of most complex diseases in humans. Developments in sequencing technology have led to the identification of a high density of rare variant single-nucleotide polymorphisms (SNPs) on the genome, each of which affects only at most 1% o...

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Bibliografiske detaljer
Main Authors: Liu, Ying, Huang, Chien Hsun, Hu, Inchi, Lo, Shaw-Hwa, Zheng, Tian
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2011
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3287829/
https://ncbi.nlm.nih.gov/pubmed/22373536
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1753-6561-5-S9-S106
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