The format is based on Keep a Changelog and this project adheres to Semantic Versioning.
- #206 - Minor patch release to fix Conda environment
- Update r-base
3.6.2
->3.6.3
- Update r-xfun
0.15
->0.20
- #171 - Minor patch release to update pipeline schema
- #138 - Add social preview image
- #153 - Add plotHeatmap
- #159 - expose bwa mem -T parameter
- nf-core/atacseq#63 - Added multicore support for Trim Galore!
- nf-core/atacseq#75 - Include gene annotation versions in multiqc report
- nf-core/atacseq#76 - featureCounts coupled to DESeq2
- nf-core/atacseq#79 - Parallelize DESeq2
- nf-core/atacseq#97 - PBC1, PBC2 from pipeline?
- nf-core/atacseq#107 - Add options to change MACS2 parameters
- Regenerated screenshots and added collapsible sections for output files in
docs/output.md
- Update template to tools
1.9
- Replace
set
withtuple
andfile()
withpath()
in all processes - Capitalise process names
- Parameters:
--bwa_min_score
to set minimum alignment score for BWA MEM--macs_fdr
to provide FDR threshold for MACS2 peak calling--macs_pvalue
to provide p-value threshold for MACS2 peak calling--skip_peak_qc
to skip MACS2 peak QC plot generation--skip_peak_annotation
to skip annotation of MACS2 and consensus peaks with HOMER--skip_consensus_peaks
to skip consensus peak generation--deseq2_vst
to use variance stabilizing transformation (VST) instead of regularized log transformation (rlog) with DESeq2--publish_dir_mode
to customise method of publishing results to output directory nf-core/tools#585
--tss_bed
parameter
- #118 - Running on with SGE
- #132 - BigWig Error: sort: cannot create temporary file in '': Read-only file system
- #154 - computeMatrix.val.mat.gz files not zipped
- nf-core/atacseq#71 - consensus_peaks.mLb.clN.boolean.intersect.plot.pdf not generated
- nf-core/atacseq#73 - macs_annotatePeaks.mLb.clN.summary.txt file is not created
- nf-core/atacseq#86 - bug in the plot_homer_annotatepeaks.r script
- nf-core/atacseq#102 - Incorrect Group ID assigned by featurecounts_deseq2.r
- nf-core/atacseq#109 - Specify custom gtf but gene bed is not generated from that gtf?
- Make executables in
bin/
compatible with Python 3
- Add bioconductor-biocparallel
1.20.0
- Add markdown
3.2.2
- Add pigz
2.3.4
- Add pygments
2.6.1
- Add pymdown-extensions
7.1
- Add python
3.7.6
- Add r-reshape2
1.4.4
- Add r-tidyr
1.1.0
- Update bedtools
2.27.1
->2.29.2
- Update bioconductor-deseq2
1.20.0
->1.26.0
- Update bioconductor-vsn
3.46.0
->3.54.0
- Update deeptools
3.2.1
->3.4.3
- Update fastqc
0.11.8
->0.11.9
- Update gawk
4.2.1
->5.1.0
- Update homer
4.9.1
->4.11
- Update macs2
2.1.2
->2.2.7.1
- Update multiqc
1.7
->1.8
- Update phantompeakqualtools
1.2
->1.2.2
- Update picard
2.19.0
->2.23.1
- Update pysam
0.15.2
->0.15.3
- Update r-base
3.4.1
->3.6.2
- Update r-ggplot2
3.1.0
->3.3.2
- Update r-lattice
0.20_35
->0.20_41
- Update r-optparse
1.6.0
->1.6.6
- Update r-pheatmap
1.0.10
->1.0.12
- Update r-scales
1.0.0
->1.1.1
- Update r-upsetr
1.3.3
->1.4.0
- Update r-xfun
0.3
->0.15
- Update samtools
1.9
->1.10
- Update subread
1.6.4
->2.0.1
- Update trim-galore
0.5.0
->0.6.5
- Update ucsc-bedgraphtobigwig
377
->357
- nf-core/atacseq#46 - Missing gene_bed path in igenomes config
- Update template to tools
1.7
- Add
--trim_nextseq
parameter - Add
CITATIONS.md
file - Capitalised process names
- Change all parameters from
camelCase
tosnake_case
(see Deprecated) - nf-core/atacseq#44 - Output directory missing: macs2/consensus/deseq2
- nf-core/atacseq#45 - Wrong x-axis scale for the HOMER: Peak annotation Counts tab plot?
- nf-core/atacseq#46 - Stage blacklist file in channel properly
- nf-core/atacseq#50 - HOMER number of peaks does not correspond to found MACS2 peaks
- Fixed bug in UpSetR peak intersection plot
- Increase default resource requirements in
base.config
- Increase process-specific requirements based on user-reported failures
- Update Nextflow
0.32.0
->19.10.0
Deprecated | Replacement |
---|---|
--design |
--input |
--singleEnd |
--single_end |
--saveGenomeIndex |
--save_reference |
--skipTrimming |
--skip_trimming |
--saveTrimmed |
--save_trimmed |
--keepDups |
--keep_dups |
--keepMultiMap |
--keep_multi_map |
--saveAlignedIntermediates |
--save_align_intermeds |
--narrowPeak |
--narrow_peak |
--saveMACSPileup |
--save_macs_pileup |
--skipDiffAnalysis |
--skip_diff_analysis |
--skipFastQC |
--skip_fastqc |
--skipPicardMetrics |
--skip_picard_metrics |
--skipPreseq |
--skip_preseq |
--skipPlotProfile |
--skip_plot_profile |
--skipPlotFingerprint |
--skip_plot_fingerprint |
--skipSpp |
--skip_spp |
--skipIGV |
--skip_igv |
--skipMultiQC |
--skip_multiqc |
Initial release of nf-core/chipseq pipeline.
- Raw read QC (FastQC)
- Adapter trimming (Trim Galore!)
- Map and filter reads (BWA, picard, SAMtools, BEDTools, BAMTools, Pysam)
- Create library-size normalised bigWig tracks (BEDTools, bedGraphToBigWig)
- Alignment QC metrics (Preseq, picard)
- ChIP-seq QC metrics (deepTools, phantompeakqualtools)
- Call and annotate broad/narrow peaks (MACS2, HOMER)
- Create consensus set of peaks per antibody (BEDTools)
- Quantification and differential binding analysis (featureCounts, DESeq2)
- Collate appropriate files for genome browser visualisation (IGV)
- Collate and present various QC metrics (MultiQC, R)