Literature DB >> 18565990

Systematic biological prioritization after a genome-wide association study: an application to nicotine dependence.

Scott F Saccone1, Nancy L Saccone, Gary E Swan, Pamela A F Madden, Alison M Goate, John P Rice, Laura J Bierut.   

Abstract

MOTIVATION: A challenging problem after a genome-wide association study (GWAS) is to balance the statistical evidence of genotype-phenotype correlation with a priori evidence of biological relevance.
RESULTS: We introduce a method for systematically prioritizing single nucleotide polymorphisms (SNPs) for further study after a GWAS. The method combines evidence across multiple domains including statistical evidence of genotype-phenotype correlation, known pathways in the pathologic development of disease, SNP/gene functional properties, comparative genomics, prior evidence of genetic linkage, and linkage disequilibrium. We apply this method to a GWAS of nicotine dependence, and use simulated data to test it on several commercial SNP microarrays. AVAILABILITY: A comprehensive database of biological prioritization scores for all known SNPs is available at http://zork.wustl.edu/gin. This can be used to prioritize nicotine dependence association studies through a straightforward mathematical formula-no special software is necessary. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Entities:  

Mesh:

Year:  2008        PMID: 18565990      PMCID: PMC2610477          DOI: 10.1093/bioinformatics/btn315

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  38 in total

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4.  The need for a systematic approach to complex pathways in molecular epidemiology.

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6.  Variants in nicotinic receptors and risk for nicotine dependence.

Authors:  Laura Jean Bierut; Jerry A Stitzel; Jen C Wang; Anthony L Hinrichs; Richard A Grucza; Xiaoling Xuei; Nancy L Saccone; Scott F Saccone; Sarah Bertelsen; Louis Fox; William J Horton; Naomi Breslau; John Budde; C Robert Cloninger; Danielle M Dick; Tatiana Foroud; Dorothy Hatsukami; Victor Hesselbrock; Eric O Johnson; John Kramer; Samuel Kuperman; Pamela A F Madden; Kevin Mayo; John Nurnberger; Ovide Pomerleau; Bernice Porjesz; Oliver Reyes; Marc Schuckit; Gary Swan; Jay A Tischfield; Howard J Edenberg; John P Rice; Alison M Goate
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2.  Prioritization of SNPs for genome-wide association studies using an interaction model of genetic variation, gene expression, and trait variation.

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Review 4.  Prioritizing GWAS results: A review of statistical methods and recommendations for their application.

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5.  [¹²⁵I]AT-1012, a new high affinity radioligand for the α3β4 nicotinic acetylcholine receptors.

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7.  SPOT: a web-based tool for using biological databases to prioritize SNPs after a genome-wide association study.

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Review 9.  Bioinformatics challenges for genome-wide association studies.

Authors:  Jason H Moore; Folkert W Asselbergs; Scott M Williams
Journal:  Bioinformatics       Date:  2010-01-06       Impact factor: 6.937

10.  Failure to replicate a genetic association may provide important clues about genetic architecture.

Authors:  Casey S Greene; Nadia M Penrod; Scott M Williams; Jason H Moore
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