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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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| Publié dans: | BMC Genomics |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2017
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| Sujets: | |
| Accès en ligne: | 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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