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remove sentieon leftovers #643

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Jul 17, 2022
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1 change: 1 addition & 0 deletions CHANGELOG.md
Original file line number Diff line number Diff line change
Expand Up @@ -148,6 +148,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
- [#562](https://github.com/nf-core/sarek/pull/562) - Restart from `--step annotate` from folder is removed. Use a `csv` file instead
- [#571](https://github.com/nf-core/sarek/pull/571) - Removed the local module `concat_vcf`.
- [#605](https://github.com/nf-core/sarek/pull/605) - Removed Scatter/gather from GATK_SINGLE_SAMPLE_GERMLINE_VARIANT_CALLING, all intervals are processed together
- [#643](https://github.com/nf-core/sarek/pull/643) - Removed Sentieon parameters

## [2.7.1](https://github.com/nf-core/sarek/releases/tag/2.7.1) - Pårtejekna

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5 changes: 2 additions & 3 deletions nextflow.config
Original file line number Diff line number Diff line change
Expand Up @@ -22,7 +22,6 @@ params {
// Main options
no_intervals = false // Intervals will be built from the fasta file
nucleotides_per_second = 1000 // Default interval size
sentieon = false // Not using Sentieon by default
tools = null // No default Variant_Calling or Annotation tools
skip_tools = null // All tools (markduplicates + baserecalibrator + QC) are used by default

Expand Down Expand Up @@ -64,8 +63,8 @@ params {
cf_minqual = 0 // ControlFreec default values
cf_window = null // by default we are not using this in Control-FREEC

pon = null // No default PON (Panel of Normals) file for GATK Mutect2 / Sentieon TNscope
pon_tbi = null // No default PON index for GATK Mutect2 / Sentieon TNscope
pon = null // No default PON (Panel of Normals) file for GATK Mutect2
pon_tbi = null // No default PON index for GATK Mutect2
ignore_soft_clipped_bases = false // no --dont-use-soft-clipped-bases for GATK Mutect2
wes = false // Set to true, if data is exome/targeted sequencing data. Used to use correct models in various variant callers
joint_germline = false // g.vcf & joint germline calling are not run by default if HaplotypeCaller is selected
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11 changes: 2 additions & 9 deletions nextflow_schema.json
Original file line number Diff line number Diff line change
Expand Up @@ -57,7 +57,7 @@
"type": "string",
"fa_icon": "fas fa-toolbox",
"description": "Tools to use for variant calling and/or for annotation.",
"help_text": "Multiple separated with commas.\n\nGermline variant calling can currently only be performed with the following variant callers:\n- FreeBayes, HaplotypeCaller, Manta, mpileup, Strelka, TIDDIT\n\nSomatic variant calling can currently only be performed with the following variant callers:\n- ASCAT, Control-FREEC, FreeBayes, Manta, MSIsensorpro, Mutect2, Strelka\n\n**NB** Mutect2 for somatic variant calling cannot be combined with `--no_intervals`\n\nTumor-only somatic variant calling can currently only be performed with the following variant callers:\n- Control-FREEC, Manta, mpileup, Mutect2, TIDDIT\n\nAnnotation is done using snpEff, VEP, or even both consecutively.\n\n> **NB** As Sarek will use bgzip and tabix to compress and index VCF files annotated, it expects VCF files to be sorted.\n\n\n\n`DNAseq`, `DNAscope` and `TNscope` are only available with `--sentieon`\n\n> **NB** tools can be specified with no concern for case.",
"help_text": "Multiple separated with commas.\n\nGermline variant calling can currently only be performed with the following variant callers:\n- FreeBayes, HaplotypeCaller, Manta, mpileup, Strelka, TIDDIT\n\nSomatic variant calling can currently only be performed with the following variant callers:\n- ASCAT, Control-FREEC, FreeBayes, Manta, MSIsensorpro, Mutect2, Strelka\n\n**NB** Mutect2 for somatic variant calling cannot be combined with `--no_intervals`\n\nTumor-only somatic variant calling can currently only be performed with the following variant callers:\n- Control-FREEC, Manta, mpileup, Mutect2, TIDDIT\n\nAnnotation is done using snpEff, VEP, or even both consecutively.\n\n> **NB** As Sarek will use bgzip and tabix to compress and index VCF files annotated, it expects VCF files to be sorted.\n\n> **NB** tools can be specified with no concern for case.",
"pattern": "^((ascat|cnvkit|controlfreec|deepvariant|dnascope|dnaseq|freebayes|haplotypecaller|manta|merge|mpileup|msisensorpro|mutect2|snpeff|strelka|tiddit|tnscope|vep)*,?)*$"
},
"no_intervals": {
Expand All @@ -73,12 +73,6 @@
"help_text": "Intervals are part of the genome chopped up, used to speed up preprocessing and variant calling.",
"default": 1000
},
"sentieon": {
"type": "boolean",
"fa_icon": "fas fa-tools",
"description": "Enable Sentieon if available.",
"help_text": "Sentieon is a commercial solution to process genomics data with high computing efficiency, fast turnaround time, exceptional accuracy, and 100% consistency.\n\n> **NB** Adds the following tools for the `--tools` options: `DNAseq`, `DNAscope` and `TNscope`."
},
"skip_tools": {
"type": "string",
"fa_icon": "fas fa-forward",
Expand Down Expand Up @@ -291,7 +285,7 @@
"pon": {
"type": "string",
"fa_icon": "fas fa-file",
"description": "Panel-of-normals VCF (bgzipped) for GATK Mutect2 / Sentieon TNscope.",
"description": "Panel-of-normals VCF (bgzipped) for GATK Mutect2",
"help_text": "Without PON, there will be no calls with PASS in the INFO field, only an unfiltered VCF is written.\nIt is recommended to make your own PON, as it depends on sequencer and library preparation.\nFor tests in iGenomes there is a dummy PON file in the Annotation/GermlineResource directory, but it should not be used as a real PON file.\n\nSee [PON documentation](https://gatk.broadinstitute.org/hc/en-us/articles/360042479112-CreateSomaticPanelOfNormals-BETA)\n> **NB** PON file should be bgzipped."
},
"pon_tbi": {
Expand Down Expand Up @@ -319,7 +313,6 @@
"type": "boolean",
"fa_icon": "fas fa-database",
"description": "Allow usage of fasta file for annotation with VEP.\ncf https://www.ensembl.org/info/docs/tools/vep/script/vep_cache.html#fasta",
"default": false,
"hidden": true
},
"vep_dbnsfp": {
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