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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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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2008
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| 主題: | |
| オンライン･アクセス: | 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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