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A genome-wide scan statistic framework for whole-genome sequence data analysis
The analysis of whole-genome sequencing studies is challenging due to the large number of noncoding rare variants, our limited understanding of their functional effects, and the lack of natural units for testing. Here we propose a scan statistic framework, WGScan, to simultaneously detect the existe...
Shranjeno v:
| izdano v: | Nat Commun |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Nature Publishing Group UK
2019
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6616627/ https://ncbi.nlm.nih.gov/pubmed/31289270 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-11023-0 |
| Oznake: |
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