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Paketti: python-htseq (0.11.2-1)

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Python 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 2 module.

Paketit, jotka toteuttavat paketin python-htseq

python3-htseq
Python3 high-throughput genome sequencing read analysis utilities

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