Adaptive Fisher method detects dense and sparse signals in association analysis of SNV sets
Abstract Background With the development of next generation sequencing (NGS) technology and genotype imputation methods, statistical methods have been proposed to test a set of genomic variants together to detect if any of them is associated with the phenotype or disease. In practice, within the set...
| Những tác giả chính: | , , , |
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| Định dạng: | Bài viết |
| Ngôn ngữ: | English |
| Được phát hành: |
BMC
2020-04-01
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| Loạt: | BMC Medical Genomics |
| Những chủ đề: | |
| Truy cập trực tuyến: | http://link.springer.com/article/10.1186/s12920-020-0684-3 |