Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs-Reference-Cited by-同舟云学术

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

Published:2008-09-07 Issue:10 Volume:40 Page:1253-1260
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Korn Joshua M,Kuruvilla Finny G,McCarroll Steven A,Wysoker Alec,Nemesh James,Cawley Simon,Hubbell Earl,Veitch Jim,Collins Patrick J,Darvishi Katayoon,Lee Charles,Nizzari Marcia M,Gabriel Stacey B,Purcell Shaun,Daly Mark J,Altshuler David

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.237.pdf

Reference22 articles.

1. Rabbee, N. & Speed, T.P. A genotype calling algorithm for affymetrix SNP arrays. Bioinformatics 22, 7–12 (2006).

2. Nicolae, D.L., Wu, X., Miyake, K. & Cox, N.J. GEL: a novel genotype calling algorithm using empirical likelihood. Bioinformatics 22, 1942–1947 (2006).

3. McCarroll, S.A. et al. Common deletion polymorphisms in the human genome. Nat. Genet. 38, 86–92 (2006).

4. Conrad, D.F., Andrews, T.D., Carter, N.P., Hurles, M.E. & Pritchard, J.K. A high-resolution survey of deletion polymorphism in the human genome. Nat. Genet. 38, 75–81 (2006).

5. McCarroll, S.A. & Altshuler, D.M. Copy-number variation and association studies of human disease. Nat. Genet. 39 (Suppl.), S37–S42 (2007).

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