[ Source: cnvkit ]
Paketti: cnvkit (0.9.12-1build1) [universe]
Links for cnvkit
Ubuntu-palvelut:
Imuroi lähdekoodipaketti cnvkit:
Ylläpitäjä:
Please consider filing a bug or asking a question via Launchpad before contacting the maintainer directly.
Original Maintainers (usually from Debian):
- Debian Med Packaging Team (Mail Archive)
- Michael R. Crusoe
- Steffen Moeller
- Olivier Sallou
It should generally not be necessary for users to contact the original maintainer.
External Resources:
- Kotisivu [cnvkit.readthedocs.org]
Samankaltaisia paketteja:
Copy number variant detection from targeted DNA sequencing
Muut pakettiin cnvkit liittyvät paketit
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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 (>= 0.15)
- 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
- R package: DNA copy number data analysis
Imuroi cnvkit
| Arkkitehtuuri | Paketin koko | Koko asennettuna | Tiedostot |
|---|---|---|---|
| all | 20,132.4 kt | 94,677.0 kt | [tiedostoluettelo] |