htseq 0.6.1p1-4 source package in Ubuntu

Changelog

htseq (0.6.1p1-4) unstable; urgency=medium

  * Tweak test for more architectures.
  * Use same repository name as source package name

 -- Andreas Tille <email address hidden>  Wed, 09 Dec 2015 12:19:39 +0100

Upload details

Uploaded by:
Debian Med on 2015-12-09
Uploaded to:
Sid
Original maintainer:
Debian Med
Architectures:
any all
Section:
misc
Urgency:
Medium Urgency

See full publishing history Publishing

Series Pocket Published Component Section
Zesty proposed on 2016-10-18 universe misc

Downloads

File Size SHA-256 Checksum
htseq_0.6.1p1-4.dsc 2.1 KiB 2ae0227e92a0899da79956ac711bfba37ad699efd5611c4c3934d06166ac3daa
htseq_0.6.1p1.orig.tar.xz 27.5 MiB 0e6955f9abb8d6c3e07e0140fccf67dd25454582469bc5195a169db025945ae7
htseq_0.6.1p1-4.debian.tar.xz 7.2 KiB 2e1428a54437b00665c8d1a608541b98e41f1a4bd134c056d002f1c0375d7b0e

Available diffs

No changes file available.

Binary packages built by this source

python-htseq: 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.

python-htseq-doc: documetation for HTSeq (high-throughput genome sequencing)

 HTSeq can be used to performing a number of common analysis tasks
 when working with high-throughput genome sequencing reads.
 .
 This package contains documentation in HTML form.