falcon: Finding Allele-Specific Copy Number in Next-Generation Sequencing Data
Version 0.2

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.

Getting started

Package details

AuthorHao Chen and Nancy R. Zhang
Date of publication2016-04-21 08:20:42
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 falcon package in your browser

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

falcon documentation built on May 30, 2017, 6:48 a.m.