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[ Source: htseq  ]

Package: python3-htseq (2.0.9+dfsg-1 and others)

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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.

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Download python3-htseq

Download for all available architectures
Architecture Version Package Size Installed Size Files
amd64 2.0.9+dfsg-1+b1 427.7 kB1,956.0 kB [list of files]
arm64 2.0.9+dfsg-1+b1 365.3 kB1,970.0 kB [list of files]
armel 2.0.9+dfsg-1+b1 369.7 kB1,818.0 kB [list of files]
armhf 2.0.9+dfsg-1+b1 374.6 kB1,562.0 kB [list of files]
i386 2.0.9+dfsg-1+b1 416.7 kB2,052.0 kB [list of files]
mips64el 2.0.9+dfsg-1+b1 329.7 kB2,144.0 kB [list of files]
ppc64el 2.0.9+dfsg-1+b1 386.9 kB2,290.0 kB [list of files]
riscv64 2.0.9+dfsg-1+b1 418.2 kB1,538.0 kB [list of files]