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Article

CaSNP: a database for interrogating copy number alterations of cancer genome from SNP array data.

Nucleic acids research - 1 Jan 2011

Cao Qingyi, Zhou Meng, Wang Xujun, Meyer Cliff A, Zhang Yong, Chen Zhi, Li Cheng, Liu X Shirley

Abstract excerpt

Cancer is known to have abundant copy number alterations (CNAs) that greatly contribute to its pathogenesis and progression. Investigation of CNA regions could potentially help identify oncogenes and tumor suppressor genes and infer cancer mechanisms. Although single-nucleotide polymorphism (SNP) arrays have strengthened our ability to identify CNAs with unprecedented resolution, a comprehensive collection of CNA...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 20972221
DOI: 10.1093/nar/gkq997
PMCID: PMC3013814

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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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