R: Somatic Copy Number Alteration Analysis Using Sequencing and...
saasCNV-package
R Documentation
Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data
Description
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.
Details
Package:
saasCNV
Type:
Package
Version:
0.3.4
Date:
2016-05-10
License:
GPL (>= 2)
See the vignettes of the package for more details.
Author(s)
Zhongyang Zhang [aut, cre], Ke Hao [aut], Nancy R. Zhang [ctb]
Zhang, Z. and Hao, K. (2015) SAAS-CNV: A joint segmentation approach on aggregated and allele specific signals
for the identification of somatic copy number alterations with next-generation sequencing Data.
PLoS Computational Biology, 11(11):e1004618.
Zhang, N. R., Siegmund, D. O., Ji, H., Li, J. Z. (2010)
Detecting simultaneous changepoints in multiple sequences. Biometrika, 97(3):631–645.