ロード中...
Parametric modeling of whole-genome sequencing data for CNV identification
Copy number variants (CNVs) constitute an important class of genetic variants in human genome and are shown to be associated with complex diseases. Whole-genome sequencing provides an unbiased way of identifying all the CNVs that an individual carries. In this paper, we consider parametric modeling...
保存先:
| 主要な著者: | , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2014
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4059462/ https://ncbi.nlm.nih.gov/pubmed/24478395 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/biostatistics/kxt060 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|