python3-htseq

Python3 high-throughput genome sequencing read analysis utilities

Description

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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Homepage

https://www-huber.embl.de/users/anders/HTSeq/doc/overview.html


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