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update versions to 1.2.8 (#3468)
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HISTORY.md

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## 1.2.8 (in progress)
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## 1.2.9 (in progress)
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## 1.2.8 (14 April 2021)
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- Set ENCODE library complexity flags properly for ChIP-seq. Thanks to @mistrm82.
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- Fix greylisted peaks not being propagated to the output directory. Thanks to @mistrm82.
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- Better error message when no sample barcodes are found for single-cell RNA-seq.
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- Enable consensus peak calling for broad peaks. Thanks to @mistrm82 and
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@yoonsquared for pointing out this was missing.
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- Re-enable ATAC-seq tests, they work now.
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- svprioritize for mm10
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- purecn_Dx.R - mutational signatures - still requires a manual update of deconstructsigs or release of it
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- make sure purecn uses sv_regions bed to call variants
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- fix misleading disambiguation fastqc read statistics (total, hg38, mm10)
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- wgbs: nebemseq kit: add --maxins 1000 and --local to bismark align
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- WGBS: sorted indexed deduplicated bam for ready.bam
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- print error message when aligner: false and hla typing is on
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- make sure that mark_duplicates is false with collapsed UMI input
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## 1.2.7 (22 February 2021)
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- RNASeq: Add gene body coverage plots to multiqc report.

LICENSE.txt

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Copyright (c) 2013 bcbio-nextgen contributors
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Copyright (c) 2013-2021 bcbio-nextgen contributors
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Permission is hereby granted, free of charge, to any person obtaining
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a copy of this software and associated documentation files (the

docs/conf.py

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# -- Project information -----------------------------------------------------
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project = 'bcbio-nextgen'
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copyright = '2020, bcbio-nextgen contributors'
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copyright = '2021, bcbio-nextgen contributors'
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author = 'bcbio-nextgen contributors'
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# The full version, including alpha/beta/rc tags
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version = release = '1.2.4'
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version = release = '1.2.8'
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# -- General configuration ---------------------------------------------------
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setup.py

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import setuptools
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VERSION = '1.2.7'
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VERSION = '1.2.8'
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# add bcbio version number and git commit hash of the current revision to version.py
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try:

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