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Support paired-end reads and custom genomes #105

Merged
merged 105 commits into from
Oct 11, 2023
Merged

Support paired-end reads and custom genomes #105

merged 105 commits into from
Oct 11, 2023

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kelly-sovacool
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@kelly-sovacool kelly-sovacool commented Sep 29, 2023

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

(Strikethrough any points that are not applicable.)

  • This comment contains a description of changes with justifications, with any relevant issues linked.
  • [ ] 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 release
  • If a new nextflow process is implemented, define the process container and stub.
  • Update CHANGELOG.md with a short description of any user-facing changes and reference the PR number. Guidelines: https://keepachangelog.com/en/1.1.0/

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.
@kelly-sovacool kelly-sovacool marked this pull request as ready for review October 11, 2023 14:17
@kelly-sovacool kelly-sovacool merged commit 509a082 into main Oct 11, 2023
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@kelly-sovacool kelly-sovacool deleted the paired-end branch October 11, 2023 14:47
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Optional subworkflow to prepare the genome Support paired-end reads
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