載入...
Detection of common single nucleotide polymorphisms synthesizing quantitative trait association of rarer causal variants
Genome-wide association (GWA) studies have identified hundreds of common (minor allele frequency ≥5%) single nucleotide polymorphisms (SNPs) associated with phenotype traits or diseases, yet causal variants accounting for the association signals have rarely been determined. A question then raised is...
Na minha lista:
| Main Authors: | , , , , |
|---|---|
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Cold Spring Harbor Laboratory Press
2011
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3129254/ https://ncbi.nlm.nih.gov/pubmed/21441355 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.115832.110 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|