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Inferring structural variant cancer cell fraction
We present SVclone, a computational method for inferring the cancer cell fraction of structural variant (SV) breakpoints from whole-genome sequencing data. SVclone accurately determines the variant allele frequencies of both SV breakends, then simultaneously estimates the cancer cell fraction and SV...
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| 發表在: | Nat Commun |
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| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Nature Publishing Group UK
2020
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7002525/ https://ncbi.nlm.nih.gov/pubmed/32024845 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-020-14351-8 |
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