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Support paired-end reads and custom genomes #105
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…s separate subworkflow
breaks for paired end
we do need to use -f 66 with ppqt. will need to fix samtools view -q 6 for bam with vishal's custom script This reverts commit caa2ec2.
it needs absolute paths in the config file
head -n 94 /data/CCBR_Pipeliner/db/PipeDB/Indices/hg38_basic/indexes/hg38.blacklist_v3.chrM.chr_rDNA.fa > tests/data/test.blacklist
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Changes
This is a major refactor with new features:
Support paired end reads. A mix of single or paired end samples can be provided in the same sample sheet, as long as each chip + input pair is the same type.
PREP_GENOME
is a new subworkflow that allows users to give a fasta and gtf file to create a custom reference genome.Custom reusable modules are pulled from CCBR/nf-modules
Issues
PR Checklist
(
Strikethroughany points that are not applicable.)[ ] Write unit tests for any new features, bug fixes, or other code changes.testing framework not yet implemented[ ] Update docs if there are any API changes.on hold until before public releasecontainer
andstub
.CHANGELOG.md
with a short description of any user-facing changes and reference the PR number. Guidelines: https://keepachangelog.com/en/1.1.0/