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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Detalles Bibliográficos
Autores principales: Lin, Chien-Hsing, Li, Ling-Hui, Ho, Sheng-Feng, Chuang, Tzu-Po, Wu, Jer-Yuarn, Chen, Yuan-Tsong, Fann, Cathy SJ
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629477/
https://www.ncbi.nlm.nih.gov/pubmed/19108714
http://dx.doi.org/10.1186/1471-2156-9-92

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629477/
https://www.ncbi.nlm.nih.gov/pubmed/19108714
http://dx.doi.org/10.1186/1471-2156-9-92

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