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Release v1.1.0 #377
Release v1.1.0 #377
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added check for case id
Update schema, output.md, and remove unused parameters
update eklipse
Release prep v1.1.0
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CHANGELOG.md
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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). | |||
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## 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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LGTM
Thanks, @maxulysse! |
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LGTM
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Nice job only some small suggestions! 🚀
docs/output.md
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@@ -296,7 +306,13 @@ The pipeline performs variant calling using [Sentieon DNAscope](https://support. | |||
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#### vcfanno | |||
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[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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[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 ) | ||
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// 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, [[:],[]] ) |
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 😉
CHROMOGRAPH_SITES([[],[]], [[],[]], [[],[]], [[],[]], [[],[]], [[],[]], UPD_SITES.out.bed) | |
CHROMOGRAPH_REGIONS([[],[]], [[],[]], [[],[]], [[],[]], [[],[]], UPD_REGIONS.out.bed, [[],[]]) | |
CHROMOGRAPH_SITES([[:],[]], [[:],[]], [[:],[]], [[:],[]], [[:],[]], [[:],[]], UPD_SITES.out.bed) | |
CHROMOGRAPH_REGIONS([[:],[]], [[:],[]], [[:],[]], [[:],[]], [[:],[]], UPD_REGIONS.out.bed, [[:],[]]) |
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QUALIMAP_BAMQC (ch_bam, []) | ||
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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 |
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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 } | ||
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DEEPVARIANT ( ch_deepvar_in, ch_fasta, ch_fai, [] ) | ||
DEEPVARIANT ( ch_deepvar_in, ch_genome_fasta, ch_genome_fai, [[],[]] ) |
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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 🚀
Thanks @JoseEspinosa and @sguizard 🙏🏻 |
PR checklist
This PR contains all the changes for release v1.1.0.
nf-core lint
).nextflow run . -profile test,docker --outdir <OUTDIR>
).nextflow run . -profile test_one_sample,docker --outdir <OUTDIR>
).docs/usage.md
is updated.docs/output.md
is updated.CHANGELOG.md
is updated.README.md
is updated (including new tool citations and authors/contributors).