[ 源代码： r-bioc-purecn ]
软件包：r-bioc-purecn（1.20.0+dfsg-3）
r-bioc-purecn 的相关链接
Debian 的资源：
下载源码包 r-bioc-purecn：
- [r-bioc-purecn_1.20.0+dfsg-3.dsc]
- [r-bioc-purecn_1.20.0+dfsg.orig.tar.xz]
- [r-bioc-purecn_1.20.0+dfsg-3.debian.tar.xz]
维护小组：
外部的资源：
- 主页 [bioconductor.org]
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copy number calling and SNV classification using targeted short read sequencing
This package estimates tumor purity, copy number, and loss of heterozygosity (LOH), and classifies single nucleotide variants (SNVs) by somatic status and clonality. PureCN is designed for targeted short read sequencing data, integrates well with standard somatic variant detection and copy number pipelines, and has support for tumor samples without matching normal samples.
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