Single Nucleotide Differences (SNDs) Continue to Contaminate the dbSNP Database With Consequences for Human Genomics and Health-Reference-Cited by-同舟云学术

Single Nucleotide Differences (SNDs) Continue to Contaminate the dbSNP Database With Consequences for Human Genomics and Health

Published:2015-02 Issue:2 Volume:36 Page:196-199
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Arthur Jonathan W.¹,Cheung Florence S.G.²,Reichardt Juergen K.V.³

Affiliation:

1. Children's Medical Research Institute; University of Sydney; Westmead New South Wales Australia

2. Department of Microbiology; Immunology Programme Centre of Life Sciences; Yong Loo Lin School of Medicine; National University of Singapore; Singapore Singapore

3. School of Pharmacy and Molecular Sciences; James Cook University; Townsville Queensland Australia

Funder

University of Sydney

Cancer Institute NSW

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22735/fullpdf

Reference15 articles.

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3. FOXO3 gene variants and human aging: coding variants may not be key players;Donlon;J Gerontol A Biol Sci Med Sci,2012

4. Using false discovery rates to benchmark SNP-callers in next-generation sequencing projects;Farrer;Sci Rep,2013

5. Unrecognized sequence homologies may confound genome-wide association studies;Galichon;Nucleic Acids Res,2012

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