htseq 0.11.2-1 source package in Ubuntu

Changelog

htseq (0.11.2-1) unstable; urgency=medium

  * New upstream version
  * debhelper 12
  * Standards-Version: 4.3.0
  * Secure URI in copyright format
  * Drop ancient X-Python-Version field

 -- Andreas Tille <email address hidden>  Fri, 11 Jan 2019 23:31:53 +0100

Upload details

Uploaded by:
Debian Med on 2019-01-12
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Eoan release on 2019-04-18 universe misc
Disco release on 2019-01-12 universe misc

Downloads

File Size SHA-256 Checksum
htseq_0.11.2-1.dsc 2.2 KiB 5c9b4c29512145d93e38bd92fac953ec442736a7884f50c6947e97a37c4427b1
htseq_0.11.2.orig.tar.gz 596.9 KiB 65c4c13968506c7df92e97124df96fdd041c4476c12a548d67350ba8b436bcfc
htseq_0.11.2-1.debian.tar.xz 10.3 KiB 3448b229f991de19782e8a503d4cc36984785f2dae930fb699f12fcfde9a1a0a

No changes file available.

Binary packages built by this source

python-htseq: 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.

python-htseq-dbgsym: debug symbols for python-htseq
python3-htseq: 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.
 .
 This package contains the Python 3 module.

python3-htseq-dbgsym: debug symbols for python3-htseq