@@ -882,10 +882,10 @@ process convertBam {
882882 params. run_convertinputbam
883883
884884 input:
885- tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, path (bam) from ch_input_for_convertbam
885+ tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, file (bam) from ch_input_for_convertbam
886886
887887 output:
888- tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, path (" *fastq.gz" ), val(' NA' ) into ch_output_from_convertbam
888+ tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, file (" *fastq.gz" ), val(' NA' ) into ch_output_from_convertbam
889889
890890 script:
891891 base = " ${ bam.baseName} "
@@ -903,10 +903,10 @@ process indexinputbam {
903903 bam != ' NA' && ! params. run_convertinputbam
904904
905905 input:
906- tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, path (bam) from ch_input_for_indexbam
906+ tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, file (bam) from ch_input_for_indexbam
907907
908908 output:
909- tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, path (bam), path (" *.{bai,csi}" ) into ch_indexbam_for_filtering
909+ tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, file (bam), file (" *.{bai,csi}" ) into ch_indexbam_for_filtering
910910
911911 script:
912912 size = " ${ params.large_ref} " ? ' -c' : ' '
@@ -935,7 +935,7 @@ process fastqc {
935935 ! params. skip_fastqc
936936
937937 input:
938- tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, path (r1), path (r2) from ch_convertbam_for_fastqc
938+ tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, file (r1), file (r2) from ch_convertbam_for_fastqc
939939
940940 output:
941941 file " *_fastqc.{zip,html}" into ch_prefastqc_for_multiqc
@@ -981,11 +981,11 @@ process fastp {
981981 params. complexity_filter_poly_g
982982
983983 input:
984- tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, path (r1), path (r2) from ch_input_for_fastp. twocol
984+ tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, file (r1), file (r2) from ch_input_for_fastp. twocol
985985
986986 output:
987- tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, path (" *.pG.fq.gz" ) into ch_output_from_fastp
988- path (" *.json" ) into ch_fastp_for_multiqc
987+ tuple samplename, libraryid, lane, colour, seqtype, organism, strandedness, udg, file (" *.pG.fq.gz" ) into ch_output_from_fastp
988+ file (" *.json" ) into ch_fastp_for_multiqc
989989
990990 script:
991991 if ( seqtype == ' SE' ){
@@ -1045,12 +1045,12 @@ process adapter_removal {
10451045 publishDir " ${ params.outdir} /AdapterRemoval" , mode: ' copy'
10461046
10471047 input:
1048- tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, path (r1), path (r2) from ch_fastp_for_adapterremoval
1048+ tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, file (r1), file (r2) from ch_fastp_for_adapterremoval
10491049
10501050 output:
1051- tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, path (" output/*{combined.fq,.se.truncated,pair1.truncated}.gz" ) into ch_output_from_adapterremoval_r1
1052- tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, path (" output/*pair2.truncated.gz" ) optional true into ch_output_from_adapterremoval_r2
1053- tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, path (" output/*.settings" ) into ch_adapterremoval_logs
1051+ tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, file (" output/*{combined.fq,.se.truncated,pair1.truncated}.gz" ) into ch_output_from_adapterremoval_r1
1052+ tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, file (" output/*pair2.truncated.gz" ) optional true into ch_output_from_adapterremoval_r2
1053+ tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, file (" output/*.settings" ) into ch_adapterremoval_logs
10541054
10551055 when:
10561056 ! params. skip_adapterremoval
@@ -1180,7 +1180,7 @@ process lanemerge {
11801180 publishDir " ${ params.outdir} /lanemerging" , mode: ' copy'
11811181
11821182 input:
1183- tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, path (r1), file(r2) from ch_branched_for_lanemerge. merge_me
1183+ tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, file (r1), file(r2) from ch_branched_for_lanemerge. merge_me
11841184
11851185 output:
11861186 tuple samplename, libraryid, lane, seqtype, organism, strandedness, udg, file(" *.fq.gz" ) into ch_lanemerge_for_mapping
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