ロード中...
Association score testing for rare variants and binary traits in family data with shared controls
Genome-wide association studies have been an important approach used to localize trait loci, with primary focus on common variants. The multiple rare variant–common disease hypothesis may explain the missing heritability remaining after accounting for identified common variants. Advances of sequenci...
保存先:
| 出版年: | Brief Bioinform |
|---|---|
| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2017
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6357552/ https://ncbi.nlm.nih.gov/pubmed/28968627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbx107 |
| 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!
|