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[ Source: cnvkit  ]

Paketti: cnvkit (0.9.12-1build1) [universe]

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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:

Samankaltaisia paketteja:

Copy number variant detection from targeted DNA sequencing

Muut pakettiin cnvkit liittyvät paketit

  • depends
  • recommends
  • suggests
  • enhances
  • dep: python3
    interactive high-level object-oriented language (default python3 version)
  • dep: python3-biopython
    Python3 library for bioinformatics
  • dep: python3-matplotlib
    Python based plotting system in a style similar to Matlab
  • dep: python3-numpy
    Python library for numerical computations (Python 3)
  • dep: python3-pandas
    data structures for "relational" or "labeled" data
  • dep: python3-pomegranate (>= 0.15)
    Fast, flexible and easy to use probabilistic modelling
  • dep: python3-pyfaidx
    efficient random access to fasta subsequences for Python 3
  • dep: python3-pysam
    interface for the SAM/BAM sequence alignment and mapping format (Python 3)
  • dep: python3-reportlab
    ReportLab library to create PDF documents using Python3
  • dep: python3-scipy
    scientific tools for Python 3
  • dep: python3-sklearn
    Python modules for machine learning and data mining - Python 3
  • dep: r-bioc-dnacopy
    R package: DNA copy number data analysis

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