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An improved burden-test pipeline for identifying associations from rare germline and somatic variants
BACKGROUND: Identifying rare germline and somatic variants associated with cancer progression is an important research topic in cancer genomics. Although many approaches are proposed for rare variant association study, they are not fit for cancer sequencing data due to multiple issues, such as overl...
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| Yayımlandı: | BMC Genomics |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5657102/ https://ncbi.nlm.nih.gov/pubmed/29513197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-017-4133-4 |
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