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Article

CNVmap: A Method and Software To Detect and Map Copy Number Variants from Segregation Data.

Genetics - 1 Mar 2020

Falque Matthieu, Jebreen Kamel, Paux Etienne, Knaak Carsten, Mezmouk Sofiane, Martin Olivier C

Abstract excerpt

Single nucleotide polymorphisms (SNPs) are used widely 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. Numerous methods and softwares based on different technologies (amplicons, CGH, tiling, or SNP...

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Identifiers

PMID: 31882400
DOI: 10.1534/genetics.119.302881
PMCID: PMC7054022

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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