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Paketti: python3-htseq (1.99.2-1 ja muut)

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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.

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Arkkitehtuuri Versio Paketin koko Koko asennettuna Tiedostot
armhf 1.99.2-1+b3 235.2 kt677.0 kt [tiedostoluettelo]