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Article

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.

Human mutation - 1 Aug 2008

Lin Chien-hsing, Huang Mei-chu, Li Ling-hui, Wu Jer-yuarn, Chen Yuan-tsong, Fann Cathy S J

Abstract excerpt

Copy number variation (CNV) has become an important genomic structure element in the human population, and some CNVs are related to specific traits and diseases. Moreover, analysis of human genomes has been potentiated by the use of high-resolution microarrays that assess single nucleotide polymo...

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PMID: 18470944
DOI: 10.1002/humu.20760

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-18470944-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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