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Article

CNstream: a method for the identification and genotyping of copy number polymorphisms using Illumina microarrays.

BMC bioinformatics - 19 May 2010

Alonso Arnald, Julià Antonio, Tortosa Raül, Canaleta Cristina, Cañete Juan D, Ballina Javier, Balsa Alejandro, Tornero Jesús, Marsal Sara

Abstract excerpt

BACKGROUND: Understanding the genetic basis of disease risk in depth requires an exhaustive knowledge of the types of genetic variation. Very recently, Copy Number Variants (CNVs) have received much attention because of their potential implication in common disease susceptibility. Copy Number Pol...

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Identifiers

PMID: 20482829
DOI: 10.1186/1471-2105-11-264
PMCID: PMC3098064

Genes

CNP

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20482829-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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CNstream: a method for the identification and genotyping of copy number polymorphisms using Illumina microarrays.PMID 20482829Read ↗

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Identification of Copy Number Variants from SNP Arrays Using PennCNV.Semantic proximity Read ↗

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PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data.Semantic proximity Read ↗

CNVineta: a data mining tool for large case-control copy number variation datasets.Semantic proximity Read ↗

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