Restore IGV [CW-7234]
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main.nf
84
main.nf
@ -228,42 +228,6 @@ workflow pipeline {
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.concat(transcriptome.joint_sqanti_dir.map { [it, "cohort"] })
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.concat(transcriptome.sample_sqanti_dirs.map { meta, sqanti_dir -> [sqanti_dir, "samples/${meta.alias}"] })
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reference_basename = file(params.ref_genome).getName()
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if (params.igv) {
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//todo ???
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//results = results
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// .concat(transcriptome.reference.map { [it, "igv_reference"] })
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// .concat(transcriptome.reference_fai.map { [it, "igv_reference"] })
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// .concat(transcriptome.reference_gzi.map { [it, "igv_reference"] })
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results = Channel.empty()
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//igv_index_paths = transcriptome.reference_fai
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// .map { "igv_reference/${it.getName()}" }
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// .concat(transcriptome.reference_gzi.map { "igv_reference/${it.getName()}" })
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igv_index_paths = Channel.empty()
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igv_alignment_paths = reads
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.map { meta, bam, bai, stat -> [
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meta.src_xam ?: "cohort/alignments/${meta.alias}/reads.bam",
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meta.src_xai ?: "cohort/alignments/${meta.alias}/reads.bam.bai"
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] }
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.flatten()
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igv_files = Channel.of("igv_reference/${reference_basename}")
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.concat(igv_index_paths)
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.concat(igv_alignment_paths)
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.collectFile(name: "igv-files.txt", newLine: true, sort: false)
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igv_conf = configure_igv(
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igv_files,
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"",
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[displayMode: "SQUISHED", colorBy: "strand"],
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[:],
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false
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)
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results = results.concat(igv_conf.map { [it, null] })
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}
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if (params.de_analysis) {
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results = results.concat(de_dir.map { [it, null] })
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}
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@ -351,11 +315,55 @@ workflow {
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throw new Exception("No samples with reads were available for transcriptome analysis.")
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}
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processed_samples = analysis_samples
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pipeline_run = pipeline(processed_samples, sample_sheet, ref_genome, ref_annotation)
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publishResults(pipeline_run.results)
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results = pipeline_run.results
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reference_basename = file(params.ref_genome).getName()
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if (params.igv) {
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results = results
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.concat(ref_genome.map { fasta, faidx -> [fasta, "igv_reference"] })
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.concat(ref_genome.map { fasta, faidx -> [faidx, "igv_reference"] })
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is_compressed = params.ref_genome.toLowerCase().endsWith("gz")
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if (is_compressed) {
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// ref files are directly publish into output
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igv_files = Channel.of("${reference_basename}")
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igv_index_paths = prepared_reference.ref_gzidx.map {
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fasta, faidx, gzidx -> "${faidx.getName()}"
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}
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.concat(prepared_reference.ref_gzidx.map {
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fasta, faidx, gzidx -> "${gzidx.getName()}"
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})
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} else {
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igv_files = Channel.of("igv_reference/${reference_basename}")
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igv_index_paths = ref_genome.map { fasta, faidx -> "igv_reference/${faidx.getName()}"}
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}
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igv_alignment_paths = processed_samples
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.map { meta, bam, bai, stat -> [
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meta.src_xam ?: "${meta.alias},cohort/alignments/${meta.alias}/reads.bam",
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meta.src_xai ?: "${meta.alias},cohort/alignments/${meta.alias}/reads.bam.bai"
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] }
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.flatten()
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igv_files = igv_files
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.concat(igv_index_paths)
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.concat(igv_alignment_paths)
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.collectFile(name: "igv-files.txt", newLine: true, sort: false)
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igv_conf = configure_igv(
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igv_files,
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"",
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[displayMode: "SQUISHED", colorBy: "strand"],
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[:],
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false
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)
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results = results.concat(igv_conf.map { [it, null] })
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}
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publishResults(results)
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}
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