載入...
Exact association test for small size sequencing data
BACKGROUND: Recent statistical methods for next generation sequencing (NGS) data have been successfully applied to identifying rare genetic variants associated with certain diseases. However, most commonly used methods (e.g., burden tests and variance-component tests) rely on large sample sizes. Not...
Na minha lista:
| 發表在: | BMC Med Genomics |
|---|---|
| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2018
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5918458/ https://ncbi.nlm.nih.gov/pubmed/29697368 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-018-0344-z |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|