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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Lin, Chien-Hsing, Li, Ling-Hui, Ho, Sheng-Feng, Chuang, Tzu-Po, Wu, Jer-Yuarn, Chen, Yuan-Tsong, Fann, Cathy SJ
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2008
Témata:
Research Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky