Releases: roryk/bcbio.rnaseq
Releases · roryk/bcbio.rnaseq
binary-only release
22 Mar 20:09
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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:
comparison of R and non-R based RNA-seq DE callers
summary reports of bcbio-nextgen RNA-seq runs
SEQC comparisons for benchmarking bcbio-nextgen RNA-seq pipeline changes
Initial pre-release.
04 Jan 14:28
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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