4.7 Article

SNPselector:: a web tool for selecting SNPs for genetic association studies

期刊

BIOINFORMATICS
卷 21, 期 22, 页码 4181-4186

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/bti682

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资金

  1. NEI NIH HHS [R01 EY13315, R01 EY012012, R01 EY013315, R01 EY12012] Funding Source: Medline
  2. NHLBI NIH HHS [P01 HL073042, P01 HL73042] Funding Source: Medline
  3. NIA NIH HHS [R01 AG021547, R01 AG19085, R01 AG019085] Funding Source: Medline
  4. NINDS NIH HHS [R01 NS31153, R01 NS031153, R01 NS036768, R01 NS36768] Funding Source: Medline

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Single nucleotide polymorphisms (SNPs) are commonly used for association studies to find genes responsible for complex genetic diseases. With the recent advance of SNP technology, researchers are able to assay thousands of SNPs in a single experiment. But the process of manually choosing thousands of genotyping SNPs for tens or hundreds of genes is time consuming. We have developed a web-based program, SNPselector, to automate the process. SNPselector takes a list of gene names or a list of genomic regions as input and searches the Ensembl genes or genomic regions for available SNPs. It prioritizes these SNPs on their tagging for linkage disequilibrium, SNP allele frequencies and source, function, regulatory potential and repeat status. SNPselector outputs result in compressed Excel spreadsheet files for review by the user.

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