falconx: Finding Allele-Specific Copy Number in Whole-Exome Sequencing Data
Version 0.2

This is a method for Allele-specific DNA Copy Number profiling for whole-Exome sequencing data. Given the allele-specific coverage and site biases 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, as well as the site biases. For detection of somatic mutations, the case and control samples can be the tumor and normal sample from the same individual. The implemented method is based on the paper: Chen, H., Jiang, Y., Maxwell, K., Nathanson, K. and Zhang, N. (under review). Allele-specific copy number estimation by whole Exome sequencing.

Getting started

Package details

AuthorHao Chen and Nancy R. Zhang
Date of publication2017-02-24 23:43:44
MaintainerHao Chen <hxchen@ucdavis.edu>
LicenseGPL (>= 2)
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:

Try the falconx package in your browser

Any scripts or data that you put into this service are public.

falconx documentation built on May 29, 2017, 1:38 p.m.