[ 源代码: cnvkit ]
软件包:cnvkit(0.9.10-3~0exp0)
cnvkit 的相关链接
Debian 的资源:
下载源码包 cnvkit:
维护小组:
- Debian Med Packaging Team (QA 页面, 邮件存档)
- Michael R. Crusoe (QA 页面)
- Steffen Moeller (QA 页面)
- Olivier Sallou (QA 页面)
外部的资源:
- 主页 [cnvkit.readthedocs.org]
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警告:这个软件包来自于 experimental 发行版。这表示它很有可能表现出不稳定或者出现 bug ,甚至是导致资料损失。请务必在使用之前查阅 changelog 以及其他潜在的文档。
Copy number variant detection from targeted DNA sequencing
A command-line toolkit and Python library for detecting copy number variants and alterations genome-wide from targeted DNA sequencing. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina and Ion Torrent.
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