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Releases: roryk/bcbio.rnaseq

binary-only release

22 Mar 20:09

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binary-only release Pre-release
Pre-release
1.2.0-binary

Dummy commit to test github integration.

1.2.0

18 Jul 19:09

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Simplified dependencies to make it installable with bioconda. Added clusterProfiler with functions to do pathway analysis. Added support for sleuth.

v1.1.1

17 Feb 20:29

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Echos the progress of the R script run. Also adds more useful failure messages when all of the necessary R libraries are not installed.

v1.1.0

17 Feb 16:34

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Updates bcbio.rnaseq to use transcript level counts from Sailfish, using Mike Love's tximport library. Adds searchable, sortable tables via the datatables R package.

v1.0.4

27 Dec 14:41

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Adds initial support for Sleuth and handling of bcbio-nextgen runs where Qualimap rnaseq could not run.

v1.0.3

16 Dec 18:30

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Preparing for installation via bioconda

Adds a --version flag for post-installation sanity checking.

v1.0.2

25 Nov 02:34

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Bug fix: Call biomaRt with a specific backup server to avoid server problems.

v1.0.1

30 Sep 16:59

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Tagging this release to get bcbio-rnaseq added to bcbio-nextgen proper.

Release 1.0

20 May 03:33

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First release supporting:

  1. comparison of R and non-R based RNA-seq DE callers
  2. summary reports of bcbio-nextgen RNA-seq runs
  3. SEQC comparisons for benchmarking bcbio-nextgen RNA-seq pipeline changes

Initial pre-release.

04 Jan 14:28

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Initial pre-release. Pre-release
Pre-release
  • When run with a SEQC dataset compares to the ~ 1000 genes abundances calculated via RT-PCR in the SEQC experiment
  • ERCC analyses are detected automatically and run
  • Output of a bcbio-nextgen run can be used to do a single factor analysis of a RNA-seq experiment