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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Detalhes bibliográficos
Main Authors: Lin, Chien-Hsing, Li, Ling-Hui, Ho, Sheng-Feng, Chuang, Tzu-Po, Wu, Jer-Yuarn, Chen, Yuan-Tsong, Fann, Cathy SJ
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2008
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Research Article
Acesso em linha: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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