Browse Source

first commit

master
biochenglinliu 3 years ago
commit
c829ad3484
6 changed files with 249 additions and 0 deletions
  1. +1
    -0
      README.md
  2. +24
    -0
      defaults
  3. +27
    -0
      inputs
  4. +68
    -0
      tasks/fastp.wdl
  5. +57
    -0
      tasks/teprof_s1.wdl
  6. +72
    -0
      workflow_run.wdl

+ 1
- 0
README.md View File

@@ -0,0 +1 @@
word.docx

+ 24
- 0
defaults View File

@@ -0,0 +1,24 @@
{
"STAR_INDEX_DIR":"oss://database-shao/teprof_star_database/GRCh38.primary_assembly_gencode.25/",
"teprof_docker":"registry.cn-shanghai.aliyuncs.com/shaolab_docker/teprof:1.5",
"teprof_cluster":"OnDemand bcs.ps.g.2xlarge img-ubuntu-vpc",
"disk_size":"300",
"fastp_docker":"registry.cn-shanghai.aliyuncs.com/shaolab_docker/teprof:1.5",
"fastp_cluster":"OnDemand bcs.ps.g.2xlarge img-ubuntu-vpc",
"trim_front1":"0",
"trim_tail1":"0",
"max_len1":"0",
"trim_front2":"0",
"trim_tail2":"0",
"max_len2":"0",
"adapter_sequence":"AGATCGGAAGAGCACACGTCTGAACTCCAGTCA",
"adapter_sequence_r2":"AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGT",
"disable_adapter_trimming":"0",
"length_required":"50",
"length_required1":"20",
"UMI":"0",
"umi_len":"0",
"umi_loc":"umi_loc",
"qualified_quality_phred":"20",
"disable_quality_filtering":"1"
}

+ 27
- 0
inputs View File

@@ -0,0 +1,27 @@
{
"{{ project_name }}.sample_id": "{{ sample_id }}",
"{{ project_name }}.fastq1": "{{ fastq1 }}",
"{{ project_name }}.fastq2": "{{ fastq2 }}",
"{{ project_name }}.STAR_INDEX_DIR": "{{ STAR_INDEX_DIR }}",
"{{ project_name }}.teprof_docker": "{{ teprof_docker }}",
"{{ project_name }}.teprof_cluster": "{{ teprof_cluster }}",
"{{ project_name }}.disk_size": "{{ disk_size }}",
"{{ project_name }}.fastp_docker": "{{ fastp_docker }}",
"{{ project_name }}.fastp_cluster": "{{ fastp_cluster }}",
"{{ project_name }}.trim_front1": "{{ trim_front1 }}",
"{{ project_name }}.trim_tail1": "{{ trim_tail1 }}",
"{{ project_name }}.max_len1": "{{ max_len1 }}",
"{{ project_name }}.trim_front2": "{{ trim_front2 }}",
"{{ project_name }}.trim_tail2": "{{ trim_tail2 }}",
"{{ project_name }}.max_len2": "{{ max_len2 }}",
"{{ project_name }}.adapter_sequence": "{{ adapter_sequence }}",
"{{ project_name }}.adapter_sequence_r2": "{{ adapter_sequence_r2 }}",
"{{ project_name }}.disable_adapter_trimming": "{{ disable_adapter_trimming }}",
"{{ project_name }}.length_required1": "{{ length_required1 }}",
"{{ project_name }}.UMI": "{{ UMI }}",
"{{ project_name }}.umi_loc": "{{ umi_loc }}",
"{{ project_name }}.umi_len": "{{ umi_len }}",
"{{ project_name }}.length_required": "{{ length_required }}",
"{{ project_name }}.qualified_quality_phred": "{{ qualified_quality_phred }}",
"{{ project_name }}.disable_quality_filtering": "{{ disable_quality_filtering }}"
}

+ 68
- 0
tasks/fastp.wdl View File

@@ -0,0 +1,68 @@
task fastp {
File read1
File read2
String sample_id
String adapter_sequence
String adapter_sequence_r2
String docker
String cluster
String disk_size
String umi_loc
Int trim_front1
Int trim_tail1
Int max_len1
Int trim_front2
Int trim_tail2
Int max_len2
Int disable_adapter_trimming
Int length_required
Int umi_len
Int UMI
Int qualified_quality_phred
Int length_required1
Int disable_quality_filtering
command <<<
mkdir -p /cromwell_root/tmp/fastp/
##1.Disable_quality_filtering
if [ "${disable_quality_filtering}" == 0 ]
then
cp ${read1} /cromwell_root/tmp/fastp/{sample_id}_R1.fastq.tmp1.gz
cp ${read2} /cromwell_root/tmp/fastp/{sample_id}_R2.fastq.tmp1.gz
else
fastp --thread 32 --trim_front1 ${trim_front1} --trim_tail1 ${trim_tail1} --max_len1 ${max_len1} --trim_front2 ${trim_front2} --trim_tail2 ${trim_tail2} --max_len2 ${max_len2} -i ${read1} -I ${read2} -o /cromwell_root/tmp/fastp/${sample_id}_R1.fastq.tmp1.gz -O /cromwell_root/tmp/fastp/${sample_id}_R2.fastq.tmp1.gz -j ${sample_id}.json -h ${sample_id}.html
fi

##2.UMI
if [ "${UMI}" == 0 ]
then
cp /cromwell_root/tmp/fastp/${sample_id}_R1.fastq.tmp1.gz /cromwell_root/tmp/fastp/${sample_id}_R1.fastq.tmp2.gz
cp /cromwell_root/tmp/fastp/${sample_id}_R2.fastq.tmp1.gz /cromwell_root/tmp/fastp/${sample_id}_R2.fastq.tmp2.gz
else
fastp --thread 32 -U --umi_loc=${umi_loc} --umi_len=${umi_len} --trim_front1 ${trim_front1} --trim_tail1 ${trim_tail1} --max_len1 ${max_len1} --trim_front2 ${trim_front2} --trim_tail2 ${trim_tail2} --max_len2 ${max_len2} -i /cromwell_root/tmp/fastp/${sample_id}_R1.fastq.tmp1.gz -I /cromwell_root/tmp/fastp/${sample_id}_R2.fastq.tmp1.gz -o /cromwell_root/tmp/fastp/${sample_id}_R1.fastq.tmp2.gz -O /cromwell_root/tmp/fastp/${sample_id}_R2.fastq.tmp2.gz -j ${sample_id}.json -h ${sample_id}.html
fi

##3.Trim
if [ "${disable_adapter_trimming}" == 0 ]
then
fastp --thread 32 -l ${length_required} -q ${qualified_quality_phred} -u ${length_required1} --adapter_sequence ${adapter_sequence} --adapter_sequence_r2 ${adapter_sequence_r2} --detect_adapter_for_pe --trim_front1 ${trim_front1} --trim_tail1 ${trim_tail1} --max_len1 ${max_len1} --trim_front2 ${trim_front2} --trim_tail2 ${trim_tail2} --max_len2 ${max_len2} -i /cromwell_root/tmp/fastp/${sample_id}_R1.fastq.tmp2.gz -I /cromwell_root/tmp/fastp/${sample_id}_R2.fastq.tmp2.gz -o ${sample_id}_R1.fastq.gz -O ${sample_id}_R2.fastq.gz -j ${sample_id}.json -h ${sample_id}.html
else
cp /cromwell_root/tmp/fastp/${sample_id}_R1.fastq.tmp2.gz ${sample_id}_R1.fastq.gz
cp /cromwell_root/tmp/fastp/${sample_id}_R2.fastq.tmp2.gz ${sample_id}_R2.fastq.gz
fi
>>>
runtime {
docker: docker
cluster: cluster
systemDisk: "cloud_ssd 40"
dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
}

output {
File json = "${sample_id}.json"
File report = "${sample_id}.html"
File Trim_R1 = "${sample_id}_R1.fastq.gz"
File Trim_R2 = "${sample_id}_R2.fastq.gz"
}
}

+ 57
- 0
tasks/teprof_s1.wdl View File

@@ -0,0 +1,57 @@
task teprof_s1 {
String sample_id
File fastq1
File fastq2
File STAR_INDEX_DIR

String disk_size
String docker
String cluster

command <<<
set -o pipefail
set -e
pigz -p 8 -dc ${fastq1} > ${sample_id}_R1.fastq
pigz -p 8 -dc ${fastq2} > ${sample_id}_R2.fastq
STAR \
--runThreadN 8 \
--genomeDir ${STAR_INDEX_DIR} \
--readFilesIn ${sample_id}_R1.fastq ${sample_id}_R2.fastq \
--outSAMstrandField intronMotif \
--outSAMtype BAM SortedByCoordinate \
--outFileNamePrefix ./${sample_id}.

samtools view -@ 8 -q 255 -h ${sample_id}.Aligned.sortedByCoord.out.bam > ${sample_id}.filtered.Aligned.sortedByCoord.out.bam
stringtie -p 8 ${sample_id}.filtered.Aligned.sortedByCoord.out.bam -o ${sample_id}.Aligned.sortedByCoord.out.gtf -m 100 -c 1 --rf
python /database/rnapipelinerefhg38/rnapipeline/rmskhg38_annotate_gtf_update_test_tpm.py ${sample_id}.Aligned.sortedByCoord.out.gtf /database/rnapipelinerefhg38/rnapipeline/arguments.txt

python /database/rnapipelinerefhg38/rnapipeline/annotationtpmprocess.py ${sample_id}.Aligned.sortedByCoord.out.gtf_annotated_filtered_test
mkdir ${sample_id}_annotated
cp ${sample_id}.Aligned.sortedByCoord.out.gtf_annotated_* ${sample_id}_annotated
tar -zcvf ${sample_id}_annotated.tgz ${sample_id}_annotated

rm ${sample_id}.filtered.Aligned.sortedByCoord.out.bam
rm ${sample_id}_R1.fastq
rm ${sample_id}_R2.fastq

>>>
runtime {
docker: docker
cluster: cluster
systemDisk: "cloud_ssd 40"
dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
}

output {
File annotated = "${sample_id}_annotated.tgz"
File annotated_use = "${sample_id}.Aligned.sortedByCoord.out.gtf_annotated_filtered_test_c"
File output_bam = "${sample_id}.Aligned.sortedByCoord.out.bam"
File output_gtf = "${sample_id}.Aligned.sortedByCoord.out.gtf"
}

}


+ 72
- 0
workflow_run.wdl View File

@@ -0,0 +1,72 @@
import "./tasks/fastp.wdl" as fastp
import "./tasks/teprof_s1.wdl" as teprof_s1

workflow run_teprof_s1 {
String sample_id
File fastq1
File fastq2
String disk_size

String fastp_docker
String fastp_cluster
String adapter_sequence
String adapter_sequence_r2
String umi_loc
Int trim_front1
Int trim_tail1
Int max_len1
Int trim_front2
Int trim_tail2
Int max_len2
Int disable_adapter_trimming
Int length_required
Int umi_len
Int UMI
Int qualified_quality_phred
Int length_required1
Int disable_quality_filtering

File STAR_INDEX_DIR
String teprof_docker
String teprof_cluster

call fastp.fastp as fastp {
input:
read1=fastq1,
read2=fastq2,
sample_id=sample_id,
docker=fastp_docker,
cluster=fastp_cluster,
disk_size=disk_size,
adapter_sequence=adapter_sequence,
adapter_sequence_r2=adapter_sequence_r2,
umi_loc=umi_loc,
trim_front1=trim_front1,
trim_tail1=trim_tail1,
max_len1=max_len1,
trim_front2=trim_front2,
trim_tail2=trim_tail2,
max_len2=max_len2,
disable_adapter_trimming=disable_adapter_trimming,
length_required=length_required,
umi_len=umi_len,
UMI=UMI,
qualified_quality_phred=qualified_quality_phred,
length_required1=length_required1,
disable_quality_filtering=disable_quality_filtering
}

call teprof_s1.teprof_s1 as teprof_s1 {
input:
sample_id=sample_id,
fastq1=fastp.Trim_R1,
fastq2=fastp.Trim_R2,
STAR_INDEX_DIR=STAR_INDEX_DIR,
disk_size=disk_size,
docker=teprof_docker,
cluster=teprof_cluster
}



}

Loading…
Cancel
Save