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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+b2 313.1 kB1,095.0 kB [list of files]
arm64 2.0.9+dfsg-1+b2 279.2 kB1,111.0 kB [list of files]
armel 2.0.9+dfsg-1+b2 279.8 kB1,035.0 kB [list of files]
armhf 2.0.9+dfsg-1+b2 285.0 kB907.0 kB [list of files]
i386 2.0.9+dfsg-1+b2 312.6 kB1,140.0 kB [list of files]
mips64el 2.0.9+dfsg-1+b2 256.2 kB1,199.0 kB [list of files]
ppc64el 2.0.9+dfsg-1+b2 300.3 kB1,303.0 kB [list of files]
riscv64 2.0.9+dfsg-1+b2 308.3 kB903.0 kB [list of files]