Use value channels for refs crossing samples
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@ -135,7 +135,8 @@ docker-run:
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NF_WORKFLOW_OPTS: "--fastq test_data/smoke/de --sample_sheet test_data/smoke/sample_sheet_de.csv --ref_genome test_data/smoke/reference.fa --ref_annotation test_data/smoke/annotation.gtf --de_analysis --reference_level control --covariates batch"
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AFTER_NEXTFLOW_CMD: >
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test -f ${CI_PROJECT_NAME}/de_analysis/condition_treated_vs_control/results_dge.tsv &&
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test -f ${CI_PROJECT_NAME}/de_analysis/condition_treated_vs_control/results_dtu_transcript.tsv
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test -f ${CI_PROJECT_NAME}/de_analysis/condition_treated_vs_control/results_dtu_transcript.tsv &&
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[ "$(find ${CI_PROJECT_NAME}/samples -type f -name 'gene_counts.tsv' | wc -l)" -eq 4 ]
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- if: $MATRIX_NAME == "invalid_mode"
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variables:
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NF_BEFORE_SCRIPT: ":"
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@ -211,8 +211,8 @@ workflow transcriptome_analysis {
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log.warn(stdoutput.trim())
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}
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}
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analysis_annotation = prepared_reference_annotation.annotation
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analysis_reference = prepared_reference_annotation.reference
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analysis_annotation = prepared_reference_annotation.annotation.first()
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analysis_reference = prepared_reference_annotation.reference.first()
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joint_bambu = runJointBambu(
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alignments
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