Tools to analyze genomic sequencing data from paired normal-tumor samples, including cellularity and ploidy estimation; mutation and copy number (allele-specific and total copy number) detection, quantification and visualization.
|Author||Francesco Favero, Andrea M. Marquard, Tejal Joshi, Aron C. Eklund|
|Maintainer||Francesco Favero <[email protected]>|
|URL||http://cbs.dtu.dk/biotools/sequenza/ Mailing list: https://groups.google.com/forum/#!forum/sequenza-user-group|
|Package repository||View on CRAN|
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