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Pakket: python3-htseq (2.0.5-1)

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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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Pakket downloaden voor alle beschikbare platforms
Platform Pakketgrootte Geïnstalleerde grootte Bestanden
amd64 477,5 kB1.837,0 kB [overzicht]
arm64 415,0 kB1.836,0 kB [overzicht]
armel 411,3 kB1.668,0 kB [overzicht]
armhf 420,4 kB1.276,0 kB [overzicht]
i386 475,3 kB1.914,0 kB [overzicht]
mips64el 378,0 kB2.076,0 kB [overzicht]
ppc64el 453,0 kB2.156,0 kB [overzicht]