[ 原始碼： r-bioc-purecn ]
套件：r-bioc-purecn（2.12.0+dfsg-1）
r-bioc-purecn 的相關連結
Debian 的資源：
下載原始碼套件 r-bioc-purecn：
- [r-bioc-purecn_2.12.0+dfsg-1.dsc]
- [r-bioc-purecn_2.12.0+dfsg.orig.tar.xz]
- [r-bioc-purecn_2.12.0+dfsg-1.debian.tar.xz]
維護小組：
外部的資源：
- 主頁 [bioconductor.org]
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試製（Experimental）套件
警告：這個套件來自於 experimental 發行版。這表示它很有可能表現出不穩定或者出現 bug ，甚至是導致資料損失。請務必在使用之前查閱 changelog 以及其他潛在的文件。
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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