A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan

BACKGROUND: Copy number variations (CNVs) have recently been recognized as important structural variations in the human genome. CNVs can affect gene expression and thus may contribute to phenotypic differences. The copy number inferring tool (CNIT) is an effective hidden Markov model-based algorithm...

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Autori principali: Lin, Chien-Hsing, Li, Ling-Hui, Ho, Sheng-Feng, Chuang, Tzu-Po, Wu, Jer-Yuarn, Chen, Yuan-Tsong, Fann, Cathy SJ
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2008
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2629477/
https://ncbi.nlm.nih.gov/pubmed/19108714
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-9-92
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