Article

CNVmap: a method and software to detect and map copy number variants from segregation data

2019-09-24

Abstract excerpt

Single nucleotide polymorphisms (SNPs) are widely used for detecting quantitative trait loci or for searching for causal variants of diseases. Nevertheless, structural variations such as copy-number variants (CNVs) represent a large part of natural genetic diversity and contribute significantly to trait variation. Over the past decade, numerous methods and softwares have been developed to detect CNVs. Such approa...

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Literature Corpus work: c61b04aa-b6e9-5dc8-9a94-a82cb32a772b
DOI: 10.1101/778753

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