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Paket: python3-htseq (1.99.2-1build1)

Python3 high-throughput genome sequencing read analysis utilities

HTSeq can be used to performing a number of common analysis tasks when working with high-throughput genome sequencing reads: 

  * Getting statistical summaries about the base-call quality scores to
    study the data quality.
  * Calculating a coverage vector and exporting it for visualization in
    a genome browser.
  * Reading in annotation data from a GFF file.
  * Assigning aligned reads from an RNA-Seq experiments to exons and
    genes.

This package contains the Python 3 module.

Andra paket besläktade med python3-htseq

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  • föreslår
  • dep: libc6 (>= 2.4)
    GNU C Library: Shared libraries
    också ett virtuellt paket som tillhandahålls av libc6-udeb
  • dep: libgcc-s1 (>= 3.5)
    GCC support library
  • dep: libstdc++6 (>= 5.2)
    GNU Standard C++ Library v3
  • dep: python3
    interactive high-level object-oriented language (default python3 version)
    dep: python3 (<< 3.11)
    dep: python3 (>= 3.10~)
  • dep: python3-numpy
    Fast array facility to the Python 3 language
  • dep: python3-pysam
    interface for the SAM/BAM sequence alignment and mapping format (Python 3)

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