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Release v1.1.0 #377

Merged
merged 211 commits into from
Jul 21, 2023
Merged

Release v1.1.0 #377

merged 211 commits into from
Jul 21, 2023

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ramprasadn
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@ramprasadn ramprasadn commented Jul 17, 2023

PR checklist

This PR contains all the changes for release v1.1.0.

  • This comment contains a description of changes (with reason).
  • If you've fixed a bug or added code that should be tested, add tests!
  • If you've added a new tool - have you followed the pipeline conventions in the contribution docs
  • If necessary, also make a PR on the nf-core/raredisease branch on the nf-core/test-datasets repository.
  • Make sure your code lints (nf-core lint).
  • Ensure the test suite passes (nextflow run . -profile test,docker --outdir <OUTDIR>).
  • Ensure the test suite passes (nextflow run . -profile test_one_sample,docker --outdir <OUTDIR>).
  • Usage Documentation in docs/usage.md is updated.
  • Output Documentation in docs/output.md is updated.
  • CHANGELOG.md is updated.
  • README.md is updated (including new tool citations and authors/contributors).

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github-actions bot commented Jul 17, 2023

nf-core lint overall result: Passed ✅ ⚠️

Posted for pipeline commit 572bee2

+| ✅ 153 tests passed       |+
#| ❔   3 tests were ignored |#
!| ❗   2 tests had warnings |!

❗ Test warnings:

  • nextflow_config - Config manifest.version should end in dev: 1.1.0
  • pipeline_todos - TODO string in awsfulltest.yml: You can customise AWS full pipeline tests as required

❔ Tests ignored:

  • files_exist - File is ignored: conf/modules.config
  • files_unchanged - File ignored due to lint config: .github/PULL_REQUEST_TEMPLATE.md
  • files_unchanged - File ignored due to lint config: .github/workflows/linting.yml

✅ Tests passed:

Run details

  • nf-core/tools version 2.9
  • Run at 2023-07-21 09:22:24

@ramprasadn ramprasadn marked this pull request as ready for review July 18, 2023 07:52
CHANGELOG.md Outdated
@@ -3,7 +3,25 @@
The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/)
and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).

## v1.0.0 - [2023-06-01]
## v1.1.0 - Abu [xxxx-xx-xx]
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Reminder to update date

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@maxulysse maxulysse left a comment

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LGTM

@ramprasadn
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Thanks, @maxulysse!

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LGTM

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Nice job only some small suggestions! 🚀

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docs/output.md Outdated
@@ -296,7 +306,13 @@ The pipeline performs variant calling using [Sentieon DNAscope](https://support.

#### vcfanno

[vcfanno](https://github.com/brentp/vcfanno) allows you to quickly annotate your VCF with any number of INFO fields from any number of VCFs. It uses a simple conf file to allow the user to specify the source annotation files and fields and how they will be added to the info of the query VCF. Values are pulled by name from the INFO field with special-cases of ID and FILTER to pull from those VCF columns. The output files are not published in the output folder by default, and is passed to vep for further annotation.
[vcfanno](https://github.com/brentp/vcfanno) allows you to quickly annotate your VCF with any number of INFO fields from any number of VCFs. It uses a simple conf file to allow the user to specify the source annotation files and fields and how they will be added to the info of the query VCF. Values are pulled by name from the INFO field with special-cases of ID and FILTER to pull from those VCF columns. The output files are not published in the output folder by default, and is passed to CADD and/or VEP for further annotation.
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Suggested change
[vcfanno](https://github.com/brentp/vcfanno) allows you to quickly annotate your VCF with any number of INFO fields from any number of VCFs. It uses a simple conf file to allow the user to specify the source annotation files and fields and how they will be added to the info of the query VCF. Values are pulled by name from the INFO field with special-cases of ID and FILTER to pull from those VCF columns. The output files are not published in the output folder by default, and is passed to CADD and/or VEP for further annotation.
[vcfanno](https://github.com/brentp/vcfanno) allows you to quickly annotate your VCF with any number of INFO fields from any number of VCFs. It uses a simple configuration file to allow the user to specify the source annotation files and fields and how they will be added to the info of the query VCF. Values are pulled by name from the INFO field with special-cases of ID and FILTER to pull from those VCF columns. The output files are not published in the output folder by default, and is passed to CADD and/or VEP for further annotation.

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SAMTOOLS_INDEX_ALIGN ( BWAMEM2_MEM.out.bam )

// Get stats for each demultiplexed read pair.
bam_sorted_indexed = BWAMEM2_MEM.out.bam.join(SAMTOOLS_INDEX_ALIGN.out.bai, failOnMismatch:true, failOnDuplicate:true)
SAMTOOLS_STATS ( bam_sorted_indexed, [] )
SAMTOOLS_STATS ( bam_sorted_indexed, [[],[]] )
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SAMTOOLS_STATS ( bam_sorted_indexed, [[],[]] )
SAMTOOLS_STATS ( bam_sorted_indexed, [[:],[]] )

Comment on lines +74 to +75
CHROMOGRAPH_SITES([[],[]], [[],[]], [[],[]], [[],[]], [[],[]], [[],[]], UPD_SITES.out.bed)
CHROMOGRAPH_REGIONS([[],[]], [[],[]], [[],[]], [[],[]], [[],[]], UPD_REGIONS.out.bed, [[],[]])
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I like to pass the empty map as [:] but up to you really 😉

Suggested change
CHROMOGRAPH_SITES([[],[]], [[],[]], [[],[]], [[],[]], [[],[]], [[],[]], UPD_SITES.out.bed)
CHROMOGRAPH_REGIONS([[],[]], [[],[]], [[],[]], [[],[]], [[],[]], UPD_REGIONS.out.bed, [[],[]])
CHROMOGRAPH_SITES([[:],[]], [[:],[]], [[:],[]], [[:],[]], [[:],[]], [[:],[]], UPD_SITES.out.bed)
CHROMOGRAPH_REGIONS([[:],[]], [[:],[]], [[:],[]], [[:],[]], [[:],[]], UPD_REGIONS.out.bed, [[:],[]])


QUALIMAP_BAMQC (ch_bam, [])

TIDDIT_COV (ch_bam, []) // 2nd pos. arg is req. only for cram input
TIDDIT_COV (ch_bam, [[],[]]) // 2nd pos. arg is req. only for cram input
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TIDDIT_COV (ch_bam, [[],[]]) // 2nd pos. arg is req. only for cram input
TIDDIT_COV (ch_bam, [[:],[]]) // 2nd pos. arg is req. only for cram input

return [meta, bam, bai, []]
}
.set { ch_deepvar_in }

DEEPVARIANT ( ch_deepvar_in, ch_fasta, ch_fai, [] )
DEEPVARIANT ( ch_deepvar_in, ch_genome_fasta, ch_genome_fai, [[],[]] )
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Suggested change
DEEPVARIANT ( ch_deepvar_in, ch_genome_fasta, ch_genome_fai, [[],[]] )
DEEPVARIANT ( ch_deepvar_in, ch_genome_fasta, ch_genome_fai, [[:],[]] )

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Awesome @ramprasadn 🚀

@ramprasadn ramprasadn merged commit 1a66422 into master Jul 21, 2023
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Thanks @JoseEspinosa and @sguizard 🙏🏻

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