polyg param improvement

CHANGELOG.md

@@ -10,6 +10,7 @@ and this project adheres to [Semantic Versioning](http://semver.org/spec/v2.0.0.
 
 ### `Fixed`
 * [#145](https://github.com/nf-core/eager/issues/145) - Added Picard Memory Handling [fix](https://github.com/nf-core/eager/issues/144)
+* Clarified `--complexity_filter` flag to be specifically for poly G trimming.
 
 
 ## [2.0.5] - 2019-01-28

conf/multiqc_config.yaml

@@ -9,6 +9,7 @@ top_modules:
             - '*_fastqc.zip'
         path_filters_exclude:
              - '*.combined.prefixed_fastqc.zip'
+     - 'fastp'
      - 'adapterRemoval'
      - 'fastqc':
          name: 'FastQC (post-AdapterRemoval)'

docs/usage.md

@@ -299,7 +299,7 @@ Turns off duplicate removal methods DeDup and MarkDuplicates respectively. No du
 
 ## Complexity Filtering Options
 
-### `--complexity_filter`
+### `--complexity_filter_poly_g`
 
 Performs a poly-G tail removal step in the beginning of the pipeline, if turned on. This can be useful for trimming ploy-G tails from short-fragments sequenced on two-colour Illumina chemistry such as NextSeqs (where no-fluorescence is read as a G on two-colour chemistry), which can inflate reported GC content values.
 

main.nf

@@ -50,7 +50,7 @@ def helpMessage() {
       --skip_deduplication
 
     Complexity Filtering 
-      --complexity_filtering            Run poly-G removal on FASTQ files
+      --complexity_filter_poly_g            Run poly-G removal on FASTQ files
       --complexity_filter_poly_g_min    Specify length of poly-g min for clipping to be performed (default: 10)
 
     Clipping / Merging
@@ -151,7 +151,7 @@ params.skip_qualimap = false
 params.skip_deduplication = false
 
 //Complexity filtering reads
-params.complexity_filter = false
+params.complexity_filter_poly_g = false
 params.complexity_filter_poly_g_min = 10
 
 //Read clipping and merging parameters
@@ -291,14 +291,14 @@ if( params.readPaths ){
             .from( params.readPaths )
             .map { row -> [ row[0], [ file( row[1][0] ) ] ] }
             .ifEmpty { exit 1, "params.readPaths or params.bams was empty - no input files supplied!" }
-            .into { ch_read_files_clip; ch_read_files_fastqc; ch_read_files_complexity_filtering }
+            .into { ch_read_files_clip; ch_read_files_fastqc; ch_read_files_complexity_filter_poly_g }
             ch_bam_to_fastq_convert = Channel.empty()
     } else if (!params.bam){
         Channel
             .from( params.readPaths )
             .map { row -> [ row[0], [ file( row[1][0] ), file( row[1][1] ) ] ] }
             .ifEmpty { exit 1, "params.readPaths or params.bams was empty - no input files supplied!" }
-            .into { ch_read_files_clip; ch_read_files_fastqc; ch_read_files_complexity_filtering }
+            .into { ch_read_files_clip; ch_read_files_fastqc; ch_read_files_complexity_filter_poly_g }
             ch_bam_to_fastq_convert = Channel.empty()
     } else {
         Channel
@@ -310,15 +310,15 @@ if( params.readPaths ){
 
             //Set up clean channels
             ch_read_files_fastqc = Channel.empty()
-            ch_read_files_complexity_filtering = Channel.empty()
+            ch_read_files_complexity_filter_poly_g = Channel.empty()
             ch_read_files_clip = Channel.empty()
     }
 } else if (!params.bam){
      Channel
         .fromFilePairs( params.reads, size: params.singleEnd ? 1 : 2 )
         .ifEmpty { exit 1, "Cannot find any reads matching: ${params.reads}\nNB: Path needs" +
             "to be enclosed in quotes!\nNB: Path requires at least one * wildcard!\nIf this is single-end data, please specify --singleEnd on the command line." }
-        .into { ch_read_files_clip; ch_read_files_fastqc; ch_read_files_complexity_filtering }
+        .into { ch_read_files_clip; ch_read_files_fastqc; ch_read_files_complexity_filter_poly_g }
         ch_bam_to_fastq_convert = Channel.empty()
 } else {
      Channel
@@ -331,7 +331,7 @@ if( params.readPaths ){
 
         //Set up clean channels
         ch_read_files_fastqc = Channel.empty()
-        ch_read_files_complexity_filtering = Channel.empty()
+        ch_read_files_complexity_filter_poly_g = Channel.empty()
         ch_read_files_clip = Channel.empty()
 
 }
@@ -548,13 +548,13 @@ process fastp {
     tag "$name"
     publishDir "${params.outdir}/FastP", mode: 'copy'
 
-    when: params.complexity_filter
+    when: params.complexity_filter_poly_g
 
     input:
-    set val(name), file(reads) from ch_read_files_complexity_filtering.mix(ch_read_files_converted_fastp)
+    set val(name), file(reads) from ch_read_files_complexity_filter_poly_g.mix(ch_read_files_converted_fastp)
 
     output:
-    set val(name), file("*pG.fq.gz") into ch_clipped_reads_complexity_filtered
+    set val(name), file("*pG.fq.gz") into ch_clipped_reads_complexity_filtered_poly_g
     file("*.json") into ch_fastp_for_multiqc
 
     script:
@@ -582,7 +582,7 @@ process adapter_removal {
     when: !params.bam
 
     input:
-    set val(name), file(reads) from ( params.complexity_filter ? ch_clipped_reads_complexity_filtered : ch_read_files_clip )
+    set val(name), file(reads) from ( params.complexity_filter_poly_g ? ch_clipped_reads_complexity_filtered_poly_g : ch_read_files_clip )
 
     output:
     file "*.combined*.gz" into (ch_clipped_reads, ch_clipped_reads_for_fastqc,ch_clipped_reads_circularmapper,ch_clipped_reads_bwamem)