R/NGScopy-package.R

## ************************************************************************
## 
## 
## 
## (c) Xiaobei Zhao
## 
## Mon Jun 16 15:53:17 EDT 2014 -0400 (Week 24)
## 
## 
## Reference: 
## 
## 
## ************************************************************************


##' NGScopy provides a quantitative caller for detecting copy number variations in next generation sequencing (NGS), including whole genome sequencing (WGS), whole exome sequencing (WES) and targeted panel sequencing (TPS). The caller can be parallelized by chromosomes to use multiple processors/cores on one computer.
##' 
##' @title NGScopy: Detection of copy number variations in next generation sequencing
##' @name NGScopy-package
##' @docType package
##' @author Xiaobei Zhao
##' @references Zhao et al (2014), Targeted Sequencing in Non-Small Cell Lung Cancer (NSCLC) Using the University of North Carolina (UNC) Sequencing Assay Captures Most Previously Described Genetic Aberrations in NSCLC, In preparation 
##' @keywords package
NULL

Try the NGScopy package in your browser

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

NGScopy documentation built on May 2, 2018, 4:08 a.m.