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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Lin, Chien-Hsing, Li, Ling-Hui, Ho, Sheng-Feng, Chuang, Tzu-Po, Wu, Jer-Yuarn, Chen, Yuan-Tsong, Fann, Cathy SJ
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2008
Aiheet:
Research Article
Linkit: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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