CNVRuler: a copy number variation-based case–control association analysis tool

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CNVRuler: a copy number variation-based case-control association analysis tool

SUMMARY The method for genome-wide association study (GWAS) based on copy number variation (CNV) is not as well established as that for single nucleotide polymorphism (SNP)-GWAS. Although there are several tools for CNV association studies, most of them do not provide appropriate definitions of CNV regions (CNVRs), which are essential for CNV-association studies. Here we present a user-friendly...

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ژورنال

عنوان ژورنال: Bioinformatics

سال: 2012

ISSN: 1460-2059,1367-4803

DOI: 10.1093/bioinformatics/bts239