This is a method for Allele-specific DNA Copy Number Profiling using Next-Generation Sequencing. Given the allele-specific coverage at the variant loci, this program segments the genome into regions of homogeneous allele-specific copy number. It requires, as input, the read counts for each variant allele in a pair of case and control samples. For detection of somatic mutations, the case and control samples can be the tumor and normal sample from the same individual.
|Author||Hao Chen and Nancy R. Zhang|
|Date of publication||2016-04-21 08:20:42|
|Maintainer||Hao Chen <firstname.lastname@example.org>|
|License||GPL (>= 2)|
|Package repository||View on CRAN|
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