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biolcl hace 3 años
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Se han modificado 6 ficheros con 239 adiciones y 0 borrados
  1. +1
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      README.md
  2. +25
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      defaults
  3. +28
    -0
      inputs
  4. +68
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      tasks/fastp.wdl
  5. +40
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      tasks/rediscoverte.wdl
  6. +77
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      workflow.wdl

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README.md Ver fichero

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word.docx

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defaults Ver fichero

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{
"salmon_index":"oss://pgx-reference-data/tediscover_salmon/Step_1_salmon_idx/",
"r_annotation":"oss://pgx-reference-data/tediscover_annotation/rollup_annotation/",
"rediscoverte_docker":"registry.cn-shanghai.aliyuncs.com/pgx-docker-registry/rediscoverte:1.7",
"rediscoverte_cluster":"OnDemand bcs.b4.3xlarge img-ubuntu-vpc",
"disk_size":"300",
"fastp_docker":"registry.cn-shanghai.aliyuncs.com/pgx-docker-registry/fastp:0.19.6",
"fastp_cluster":"OnDemand bcs.b4.3xlarge 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"
}

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inputs Ver fichero

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{
"{{ project_name }}.sample_id": "{{ sample_id }}",
"{{ project_name }}.fastq1": "{{ fastq1 }}",
"{{ project_name }}.fastq2": "{{ fastq2 }}",
"{{ project_name }}.salmon_index": "{{ salmon_index }}",
"{{ project_name }}.r_annotation": "{{ r_annotation }}",
"{{ project_name }}.rediscoverte_docker": "{{ rediscoverte_docker }}",
"{{ project_name }}.rediscoverte_cluster": "{{ rediscoverte_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 }}"
}

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tasks/fastp.wdl Ver fichero

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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 16 --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/${sample_id}_R2.fastq.tmp2.gz
else
fastp --thread 16 -U --umi_loc=${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 16 -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"
}
}

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tasks/rediscoverte.wdl Ver fichero

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task rediscoverte {
String sample_id
File fastq1
File fastq2
File salmon_index
File r_annotation

String disk_size
String docker
String cluster

command <<<
set -o pipefail
set -e

mkdir ./output/
/software/Salmon-0.8.2_linux_x86_64/bin/salmon quant --seqBias --gcBias -i ${salmon_index} -l ISR -1 ${fastq1} -2 ${fastq2} -p 28 -o Step_2_salmon_counts
echo -e "sample\tquant_sf_path" > Step_3_metadata_for_rollup.tsv.txt
echo -e "${sample_id}\tStep_2_salmon_counts/quant.sf" >> Step_3_metadata_for_rollup.tsv.txt
cp -r ${r_annotation} ./
cp /software/REdiscoverTE/a.Rdata ./
/opt/conda/bin/Rscript /software/REdiscoverTE/rollup.R

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

output {
Array[File] te_result=glob("./Step_4_rollup2/*.RDS")
}

}



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workflow.wdl Ver fichero

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import "./tasks/fastp.wdl" as fastp
import "./tasks/rediscoverte.wdl" as rediscoverte

workflow {{ project_name }} {
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 salmon_index
File r_annotation
String rediscoverte_docker
String rediscoverte_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 rediscoverte.rediscoverte as rediscoverte {
input:
sample_id=sample_id,
fastq1=fastp.Trim_R1,
fastq2=fastp.Trim_R2,
salmon_index=salmon_index,
r_annotation=r_annotation,
disk_size=disk_size,
docker=rediscoverte_docker,
cluster=rediscoverte_cluster
}



}

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