Python3 high-throughput genome sequencing read analysis utilities
DescriptionHTSeq 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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