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Merge pull request nf-core#1329 from drpatelh/updates
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Remove tags from all nf-test files
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drpatelh authored Jun 20, 2024
2 parents 579684a + 9dbdd2c commit 53e59a8
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1 change: 1 addition & 0 deletions CHANGELOG.md
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Expand Up @@ -93,6 +93,7 @@ Thank you to everyone else that has contributed by reporting bugs, enhancements
- [PR #1324](https://github.com/nf-core/rnaseq/pull/1324) - Fix tags entries and rename pipeline level tests
- [PR #1325](https://github.com/nf-core/rnaseq/pull/1325) - Minor fixes to strandedness settings and messaging
- [PR #1326](https://github.com/nf-core/rnaseq/pull/1326) - Move Conda dependencies for local modules to individual environment file
- [PR #1329](https://github.com/nf-core/rnaseq/pull/1329) - Remove tags from all nf-test files

### Parameters

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1 change: 0 additions & 1 deletion modules/local/star_align_igenomes/tests/main.nf.test
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Expand Up @@ -3,7 +3,6 @@ nextflow_process {
name "Test Process STAR_ALIGN_IGENOMES"
script "../main.nf"
process "STAR_ALIGN_IGENOMES"
tag "STAR_GENOMEGENERATE_IGENOMES"

setup {
run("STAR_GENOMEGENERATE_IGENOMES") {
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1 change: 0 additions & 1 deletion modules/nf-core/custom/tx2gene/tests/main.nf.test

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2 changes: 0 additions & 2 deletions modules/nf-core/hisat2/align/tests/main.nf.test

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1 change: 0 additions & 1 deletion modules/nf-core/hisat2/build/tests/main.nf.test

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1 change: 0 additions & 1 deletion modules/nf-core/kallisto/quant/tests/main.nf.test

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1 change: 0 additions & 1 deletion modules/nf-core/salmon/quant/tests/main.nf.test

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1 change: 0 additions & 1 deletion modules/nf-core/star/align/tests/main.nf.test

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2 changes: 0 additions & 2 deletions modules/nf-core/tximeta/tximport/tests/main.nf.test

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5 changes: 0 additions & 5 deletions subworkflows/local/align_star/tests/main.nf.test
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Expand Up @@ -4,11 +4,6 @@ nextflow_workflow {
script "../main.nf"
workflow "ALIGN_STAR"
config "./nextflow.config"
tag "STAR_GENOMEGENERATE"
tag "STAR_GENOMEGENERATE_IGENOMES"
tag "STAR_ALIGN"
tag "STAR_ALIGN_IGENOMES"
tag "BAM_SORT_STATS_SAMTOOLS"

test("star - no igenomes") {

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17 changes: 0 additions & 17 deletions subworkflows/local/prepare_genome/tests/main.nf.test
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Expand Up @@ -4,23 +4,6 @@ nextflow_workflow {
script "../main.nf"
workflow "PREPARE_GENOME"
config "./nextflow.config"
tag "BBMAP_BBSPLIT"
tag "CUSTOM_CATADDITIONALFASTA"
tag "CUSTOM_GETCHROMSIZES"
tag "GFFREAD"
tag "GTF2BED"
tag "GTF_FILTER"
tag "GUNZIP"
tag "HISAT2_BUILD"
tag "HISAT2_EXTRACTSPLICESITES"
tag "KALLISTO_INDEX"
tag "PREPROCESS_TRANSCRIPTS_FASTA_GENCODE"
tag "RSEM_PREPAREREFERENCE"
tag "SALMON_INDEX"
tag "SORTMERNA"
tag "STAR_GENOMEGENERATE"
tag "STAR_GENOMEGENERATE_IGENOMES"
tag "UNTAR"

test("default options") {

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4 changes: 0 additions & 4 deletions subworkflows/local/quantify_rsem/tests/main.nf.test
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Expand Up @@ -4,10 +4,6 @@ nextflow_workflow {
script "../main.nf"
workflow "QUANTIFY_RSEM"
config "./nextflow.config"
tag "RSEM_PREPAREREFERENCE"
tag "RSEM_CALCULATEEXPRESSION"
tag "RSEM_MERGE_COUNTS"
tag "BAM_SORT_STATS_SAMTOOLS"

test("homo_sapiens") {

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Expand Up @@ -2,7 +2,6 @@ nextflow_function {

name "Test Functions"
script "../main.nf"
tag "UTILS_NFCORE_RNASEQ_PIPELINE"

test("Test Function checkSamplesAfterGrouping success") {

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Expand Up @@ -3,7 +3,6 @@ nextflow_workflow {
name "Test Workflow PIPELINE_COMPLETION"
script "../main.nf"
workflow "PIPELINE_COMPLETION"
tag "UTILS_NFCORE_RNASEQ_PIPELINE"

test("test PIPELINE_COMPLETION successfully completes") {

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8 changes: 0 additions & 8 deletions subworkflows/nf-core/bam_rseqc/tests/main.nf.test

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3 changes: 0 additions & 3 deletions subworkflows/nf-core/bam_stats_samtools/tests/main.nf.test

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4 changes: 0 additions & 4 deletions subworkflows/nf-core/fastq_align_hisat2/tests/main.nf.test

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2 changes: 0 additions & 2 deletions tests/default.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline with default settings"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: default") {

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2 changes: 0 additions & 2 deletions tests/featurecounts_group_type.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline without a group type for featureCounts"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: --featurecounts_group_type false") {

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2 changes: 0 additions & 2 deletions tests/kallisto.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline with Kallisto, skipping both QC and alignment"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: --pseudo_aligner kallisto --skip_qc --skip_alignment") {

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2 changes: 0 additions & 2 deletions tests/min_mapped_reads.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline with a minimum mapped read threshold of 90"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: --min_mapped_reads 90") {

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2 changes: 0 additions & 2 deletions tests/remove_ribo_rna.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline with ribosomal RNA removal"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: --remove_ribo_rna") {

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2 changes: 0 additions & 2 deletions tests/salmon.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline with Salmon, skipping both QC and alignment"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: --pseudo_aligner salmon --skip_qc --skip_alignment") {

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2 changes: 0 additions & 2 deletions tests/skip_qc.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline by skipping QC options"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: --skip_qc") {

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2 changes: 0 additions & 2 deletions tests/skip_trimming.nf.test
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Expand Up @@ -2,8 +2,6 @@ nextflow_pipeline {

name "Test pipeline by skipping trimming options"
script "../main.nf"
tag "RNASEQ"
tag "PIPELINE"

test("Params: --skip_trimming") {

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