R package for clustering and estimating cancer cell fractions (CCF) of somatic variants (SNVs/SVs) from bulk whole genome/exome data.
https://anaconda.org/bioconda/r-ccube/badges/version.svg
https://anaconda.org/bioconda/r-ccube/badges/latest_release_date.svg
https://anaconda.org/bioconda/r-ccube/badges/latest_release_relative_date.svg
https://anaconda.org/bioconda/r-ccube/badges/platforms.svg
https://anaconda.org/bioconda/r-ccube/badges/license.svg
https://anaconda.org/bioconda/r-ccube/badges/downloads.svg