[ 原始碼： cnvkit ]
套件：cnvkit（0.9.10-3~0exp0）
cnvkit 的相關連結
Debian 的資源：
下載原始碼套件 cnvkit：
維護小組：
- Debian Med Packaging Team (QA 頁面, 郵件存檔)
- Michael R. Crusoe (QA 頁面)
- Steffen Moeller (QA 頁面)
- Olivier Sallou (QA 頁面)
外部的資源：
- 主頁 [cnvkit.readthedocs.org]
相似套件：
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 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.
其他與 cnvkit 有關的套件
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- dep: python3
- interactive high-level object-oriented language (default python3 version)
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- dep: python3-biopython
- Python3 library for bioinformatics
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- dep: python3-matplotlib
- Python based plotting system in a style similar to Matlab
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- dep: python3-numpy
- Python library for numerical computations (Python 3)
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- dep: python3-pandas
- data structures for "relational" or "labeled" data
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- dep: python3-pomegranate
- Fast, flexible and easy to use probabilistic modelling
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- dep: python3-pyfaidx
- efficient random access to fasta subsequences for Python 3
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- dep: python3-pysam
- interface for the SAM/BAM sequence alignment and mapping format (Python 3)
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- dep: python3-reportlab
- ReportLab library to create PDF documents using Python3
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- dep: python3-scipy
- scientific tools for Python 3
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- dep: python3-sklearn
- Python modules for machine learning and data mining - Python 3
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- dep: r-bioc-dnacopy (>= 1.78.0)
- R package: DNA copy number data analysis