bugfixes and minor changes

TOuCAN.nf

@@ -116,7 +116,6 @@ Usage: nextflow run TOuCAN.nf --in [Input Path] --out [Output Path] --mode [Modi
         --hic_thresh_min [(-)INT]   - Threshold filter miniumum [default: -1.5]
         --hic_thresh_max [INT]      - Threshold filter maximum [default: 5]
         --inputBufferSize [INT]     - Buffersize for creating hic matrix [default: 400000]
-        --bt2_index_threads [INT]   - Number of threads used or creating bt2 index
 
 Skip Aligment -> BAM files as Input:
 The BAM files need to be from this Pipeline with follwing
@@ -172,10 +171,10 @@ Path to bin: ${path_bin}
 Path to genome: ${path_genome}
 Path to restriction maps: ${path_T2C_restriction_maps}
 """
-if ( ! params.bam == "" ){
-    log.info """
-    Path to bam files: ${params.bam}
-    """
+if ( "${params.bam}" != "" ){
+log.info"""
+Path to bam files: ${params.bam}
+"""
 }
 
 log.info """
@@ -197,7 +196,7 @@ multiplot_bed_1 = Channel.empty()
 matrix_to_plot = Channel.empty()
 res_map = Channel.empty()
 bam_f = Channel.empty()
-bam_f2 = Channel.empty()
+bam2 = Channel.empty()
 interaction_uropa = Channel.empty()
 fastqGzFiles = Channel.empty()
 hic_matrix_f = Channel.empty()
@@ -242,8 +241,15 @@ if (params.mode != "plot"){
 		Channel
 			.fromPath("${params.bam}/*.bam")
 			.map {it -> [it.simpleName, it]}
-            .into {bam_f; bam_f2}
+            .set {bam_f}
 		create_bam = false
+        if("${params.mode}" == "HiC"){
+            Channel
+    			.fromPath("${params.bam}/*.bam")
+    			.map {it -> [it.simpleName.replaceAll(params.sample_extension, ""), it]}
+                .set {bam2}
+            create_bam = false
+        }
 	} else if ("${params.mode}" == "HiC" & "${params.mode}" == "h5") {
         hic_matrix_f = Channel
                             .fromPath("${params.in}/*.h5")
@@ -437,7 +443,7 @@ process decompress {
 
 	output:
 	set basisname, fastqName ,file ("${fastqName}.fastq") into decompressedfastq, decompressedfastq_for_HiC_bwa,
-                                                               decompressedfastq_for_HiC_bowtie2, decompressedfastq_for_HiC_histat
+                                                               decompressedfastq_for_HiC_bowtie2
 
 	script:
 	fastqName = fastqGz.simpleName
@@ -675,7 +681,7 @@ process index_bamfiles {
 	set name, file (bam) from finalbam
 
 	output:
-	set name, file ("${name}.bam.bai") into bam_bai_files, test
+	set name, file ("${name}.bam.bai") into bam_bai_files
 
 	when:
 	params.mode == "T2C"
@@ -960,19 +966,17 @@ process finalize_matrix {
 	set name, file (temp_bed) from temp_bed_file
 
 	output:
-	set name, file ("${name_raw}.reassigned.bed") into reassigned_matrix
-	set name_raw, file ("${name_raw}.reassigned.bed") into reassigned_matrix_raw
+	set name, file ("${name}.reassigned.bed") into reassigned_matrix
 
 	when:
 	params.mode == "T2C"
     params.reassin == 1
 
 	script:
-	name_raw =  "${name}_raw"
 	"""
 	cat ${temp_bed} | \
 		sort -k 1,1 -k 2,2n -k 4,4 -k 5,5n |\
-			${path_python}/python ${path_bin}/bin/aggregate_matrix.py -o ${name_raw}.reassigned.bed
+			${path_python}/python ${path_bin}/bin/aggregate_matrix.py -o ${name}.reassigned.bed
 	"""
 }
 
@@ -1008,7 +1012,7 @@ process normalize_matrix {
     	--method ${params.norm_method}
 	"""
 }
-to_plot = matrix_to_plot.concat(normalized_matrix).concat(reassigned_matrix_raw)
+to_plot = matrix_to_plot.concat(normalized_matrix)
 
 
 /*
@@ -1159,7 +1163,7 @@ process create_uropa_config_1 {
 process run_uropa_1 {
 
 	tag{name}
-    conda "$workflow.projectDir/uropa.yaml"
+    //conda "$workflow.projectDir/envtoucan.yaml"
 
     if(params.safe_all_files == 1){
 	       publishDir "${outpath}/${params.pn}_uropa/", mode: 'copy'
@@ -1258,7 +1262,7 @@ process create_uropa_config_2 {
 process run_uropa_2 {
 
 	tag{name}
-    conda "$workflow.projectDir/uropa.yaml"
+    //conda "$workflow.projectDir/envtoucan.yaml"
 
     if(params.safe_all_files == 1){
            publishDir "${outpath}/${params.pn}_uropa/", mode: 'copy'
@@ -1446,7 +1450,11 @@ process plot_TAD_graph {
 
 }
 
-multiplot_bed_merged = multiplot_bed_1.concat(multiplot_bed_2)
+multiplot_bed_1.concat(multiplot_bed_2).into {multiplot_bed_merged; testa}
+
+multiplot_TAD.join(multiplot_bed_merged).into {multi; testb}
+testa.println()
+testb.println()
 
 process multiplot {
 
@@ -1455,8 +1463,7 @@ process multiplot {
 	publishDir "${outpath}/${params.pn}_plots/multiplot/", mode: 'copy'
 
 	input:
-	set name, file (tad) from multiplot_TAD
-	set name, file (bed) from multiplot_bed_merged
+	set name, file (tad), file (bed) from multi
 
 	output:
 	file ("*.png") into for_pptx
@@ -1522,8 +1529,7 @@ process alignment_with_bwa {
 	set basisname, file ("${fastqName}.bam") into bwa_alignment
 
 	when:
-	params.mode == "HiC" && params.aln == "bwa"
-    create_bam == true
+	params.mode == "HiC" && params.aln == "bwa" && create_bam == true
 
 	script:
 	"""
@@ -1549,9 +1555,26 @@ process bowtie2_index {
 	script:
 	genome_file = file (path_genome)
 	genome_name = genome_file.name
-	"""
-	bowtie2-build ${path_genome} ${genome_name} --threads ${params.bt2_index_threads}
-	"""
+
+    indx = file ("${path_genome}").getBaseName()
+    path = file ("${path_genome}").getParent()
+    i = "${path}/bowtie2/${indx}"
+
+    bt1 = file("${i}.1.bt2")
+    bt2 = file("${i}.2.bt2")
+    bt3 = file("${i}.3.bt2")
+    bt4 = file("${i}.4.bt2")
+    rev1 = file("${i}.rev.1.bt2")
+    rev2 = file("${i}.rev.2.bt2")
+
+    if(bt1.exists() && bt2.exists() && bt3.exists() && bt4.exists() && rev1.exists() && rev2.exists())
+        """
+        echo "Skiped creating bt2 index"
+        """
+    else
+	    """
+	    bowtie2-build ${path_genome} ${genome_name} --threads ${params.bt2_index_threads}
+	    """
 }
 
 
@@ -1562,23 +1585,24 @@ process alignment_with_bowtie2 {
     conda "$workflow.projectDir/envtoucan.yaml"
 
 	input:
-	set basisname, fastqName ,file (fastq) from decompressedfastq_for_HiC_bowtie2
-    val bt2_idx from index_bt2
+	set basisname, fastqName ,file (fastq), bt2_idx from decompressedfastq_for_HiC_bowtie2.combine(index_bt2)
 
 	output:
-	set basisname, file ("${fastqName}.bam") into bowtie2_alignment
+	set basisname, file ("${fastqName}.sam") into bowtie2_alignment
 
 	when:
 	params.mode == "HiC" && params.aln == "bowtie2" && create_bam == true
 
 	script:
+    indx = file ("${path_genome}").getBaseName()
+    path = file ("${path_genome}").getParent()
+    i = "${path}/bowtie2/${indx}"
 	"""
-	bowtie2 -x ${path_genome} -U ${fastq} --very-sensitive -L 30 --score-min L,-0.6,-0.2 --end-to-end --reorder -p 12 \
-	| samtools view -Shb - > ${fastqName}.bam
+	bowtie2 -x ${i} -U ${fastq} --very-sensitive --reorder -p ${params.threads_bowtie2} > ${fastqName}.sam
 	"""
 }
 
-hic_alignment = bam_f2.concat(bwa_alignment.concat(bowtie2_alignment)) //.concat(histat_alignment)
+bam2.concat(bwa_alignment, bowtie2_alignment).set {hic_alignment}
 
 process create_HiC_matrix {
 
@@ -1590,7 +1614,7 @@ process create_HiC_matrix {
 
 	output:
 	set name, file("${name}_matrix.h5") into hic_matrix, hic_matrix_for_diagnostic
-	file ("${name}.bam") into hic_bam
+	file ("${name}.bam")
 
 	when:
 	params.mode == "HiC"
@@ -1606,11 +1630,12 @@ process create_HiC_matrix {
     }
 	"""
 	hicBuildMatrix --samFiles ${bam_r1} ${bam_r2} \
-				 --QCfolder ${outpath}/QC_${name}/  \
+				 --QCfolder ${outpath}/${params.pn}_QC_${name}/  \
                  --binSize ${params.bin} \
 				 -b ${name}.bam \
                  --inputBufferSize ${params.inputBufferSize} \
                  --restrictionSequence ${params.enzyme_a_sequence} \
+                 --threads ${params.hicBuildMatrix_threads}\
                  -o ${name}_matrix.h5
 
 	"""
@@ -1626,7 +1651,7 @@ process diagnostic_plot_of_HiC_Matrix {
 	set name, file (matrix) from hic_matrix_for_diagnostic
 
 	output:
-	set name, file ("${name}.png") // into hic_matrix_corrected
+	set name, file ("${name}.png")
 
 	when:
 	params.mode == "HiC"
@@ -1642,7 +1667,7 @@ hic_matrix_final = hic_matrix_f.concat(hic_matrix)
 process correct_matrix {
 
     tag{name}
-    publishDir "${outpath}/${params.pn}_h5_matrix/", mode: 'copy'
+    publishDir "${outpath}/${params.pn}_h5_matrix/corrected/", mode: 'copy'
 
     input:
     set name, file (matrix) from hic_matrix_final

envtoucan.yaml

@@ -7,4 +7,6 @@ dependencies:
   - bwa=0.7.15
   - samtools=1.3.1
   - bedtools=2.27.1
-  - bowtie2=2.3.3.1
+  - bowtie2=2.3.4.1
+  - python=2.7
+  - perl=5.26.0

nextflow.config

@@ -15,7 +15,7 @@ env {
 }
 
 params {
-	sample_extension = "_R[12]_001" // regex for sample extension [e.g "_R[12]_001" or "_R[12]"]
+	sample_extension = "_R[12]" // regex for sample extension [e.g "_R[12]_001" or "_R[12]"]
 
 	// Enzyme Information
 	// -------------------------------------------
@@ -26,23 +26,25 @@ params {
 
 	// Minor fixed parameters for BWA and SAMtools
 	// -------------------------------------------
-	bwa_T2C_options = "-t 16" // bwa aln
-	sort_options = "--threads 16"
+	bwa_T2C_options = "-t 32" // bwa aln
+	sort_options = "--threads 32"
 	library_label = "capture"
 	platform_label = "ILLUMINA"
 	center_label = "ECB"
 
 	//Parameter for normalization and plotting T2C
 	// -------------------------------------------
 	plot_options_T2C = ""
-	norm_method = "FPM" //log, fpm, array and none
+	norm_method = "array" //log, fpm, array and none
 
 	uropa_threads = 32
 
 	//Parameter for HiC matrix
 	//--------------------------------------------
-	hicBuildMatrix_options = "--threads 16 --inputBufferSize 100000"
+	hicBuildMatrix_threads = 16
 	bwa_HiC_options = "-t 4" // bwa mem
+	threads_bowtie2 = 12
+	inputBufferSize = 400000
 
 	//Parameter for uropa configuration
 	uropa_feature = "" // "String,String,String,..."