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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...
Gorde:
| Argitaratua izan da: | Nat Commun |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Nature Publishing Group UK
2019
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| Gaiak: | |
| Sarrera elektronikoa: | 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 |
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