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Article

MPAgenomics: an R package for multi-patient analysis of genomic markers.

BMC bioinformatics - 14 Dec 2014

Grimonprez Quentin, Celisse Alain, Blanck Samuel, Cheok Meyling, Figeac Martin, Marot Guillemette

Abstract excerpt

BACKGROUND: Last generations of Single Nucleotide Polymorphism (SNP) arrays allow to study copy-number variations in addition to genotyping measures. RESULTS: MPAgenomics, standing for multi-patient analysis (MPA) of genomic markers, is an R-package devoted to: (i) efficient segmentation and (ii) selection of genomic markers from multi-patient copy number and SNP data profiles. It provides wrappers from commonly...

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Share to DNA Copy Number Variations
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 25495450
DOI: 10.1186/s12859-014-0394-y
PMCID: PMC4269855

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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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