This package offers a direct method to accurately quantify the cellular prevalence of somatic mutations in cancer using phase information. The method utilizes three sources of information: the phasing information, the copy number variation, and the allele counts. The method is demonstrated to bring more capabilities in Cancer Genomic.
Package details |
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Maintainer | |
License | GPL-2 |
Version | 0.1 |
Package repository | View on GitHub |
Installation |
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