Frequency Finder: a multi-source web application for collection of public allele frequencies of SNP markers

被引:5
|
作者
Nguyen, TH
Liu, CY
Gershon, ES
McMahon, FJ
机构
[1] Univ Chicago, Dept Psychiat, Chicago, IL 60616 USA
[2] Cent S Univ, Natl Lab Med Genet China, Changsha 410078, Peoples R China
[3] NIMH, Mood & Anxiety Disorder Program, NIH, US Dept HHS, Bethesda, MD 20892 USA
关键词
D O I
10.1093/bioinformatics/btg446
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Publicly available single nucleotide polymorphism (SNP) allele frequencies are an important resource for the selection of genetic markers that may be most useful for gene mapping and association studies. Data mining these allele frequencies through disparate public databases and Websites is time consuming and can result in inconsistent findings. We have developed a web-based software tool, Frequency Finder, to acquire SNP allele frequencies from multiple public data sources and return a summarized result to the user. Our software optimizes and automates the search of candidate markers, decreasing the amount of time it would take to extract pertinent data manually. We have included several methods to output the data, including on-screen and as a compressed text file. We show that Frequency Finder accurately retrieves available frequency data from the available sources. Using this tool, we detect significant differences between Asian, African and Caucasian populations in the allele frequency spectra of 246 097 SNPs. While limited to public databases that provide web-based access to allele frequencies, Frequency Finder provides a single, user-friendly interface for retrieving allele frequencies for large batches of SNPs from multiple data sources.
引用
收藏
页码:439 / 443
页数:5
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