saasCNV

cranv0.3.4

Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data. Perform joint segmentation on two signal dimensions derived from total read depth (intensity) and allele specific read depth (intensity) for whole genome sequencing (WGS), whole exome sequencing (WES) and SNP array data.

License GPL (>= 2)0 versions1 maintainers2 deps60 weekly dl
https://CRAN.R-project.org/package=saasCNV
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RANNDNAcopy
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First published · 2016-05-17 20:06:21

Last updated · 2016-05-18T02:04:56+00:00