Release v0.5.3
Automated preprocessing of Next-Generation Sequencing data, including full (sc)ATAC-seq, ChIP-seq, and RNA-seq workflows.
Added
- DESeq2 blind sample distance & correlation cluster heatmaps for RNA-, ATAC- ChIP-seq counts
- find them annotated in the MultiQC when running >1 sample
Changed
- "biological_replicate" and "technical_replicate" renamed to *"_replicates" (matches between samples.tsv & config.yaml)
- fixed bug with seq2science making a {output.allsizes} file
- Changed explain to use 'passive style'
- Genrich peak calling defaults
- Doesn't remove PCR duplicates anymore (best to do with markduplicates)
- Changed extsize to 200 to be similar to macs settings
- Turned off tn5 shift, since that is done by seq2science
Fixed
- depend less on local genomes (only when data is unavailable online)
- trackhub explanation was missing, added
- bug with broad peaks and qc that could not be made