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gatk4_hc_check.sh
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#! /bin/bash
#########################################################
#
# Platform: NCI Gadi HPC
# Usage:
# Version: 2.0
#
# For more details see: https://github.com/Sydney-Informatics-Hub/Germline-ShortV
#
# If you use this script towards a publication, support us by citing:
#
# Suggest citation:
# Sydney Informatics Hub, Core Research Facilities, University of Sydney,
# 2021, The Sydney Informatics Hub Bioinformatics Repository, <date accessed>,
# https://github.com/Sydney-Informatics-Hub/Germline-ShortV
#
# Please acknowledge the Sydney Informatics Hub and the facilities:
#
# Suggested acknowledgement:
# The authors acknowledge the technical assistance provided by the Sydney
# Informatics Hub, a Core Research Facility of the University of Sydney
# and the Australian BioCommons which is enabled by NCRIS via Bioplatforms
# Australia. The authors acknowledge the use of the National Computational
# Infrastructure (NCI) supported by the Australian Government.
#
#########################################################
config=''
if [ -z "${config}" ]
then
if [ -z "$1" ]
then
echo "Please run this script with the path to your <cohort>.config e.g. sh gatk4_hc_make_input.sh ../cohort.config"
exit
else
config=$1
fi
fi
config=$1
cohort=$(basename $config | cut -d'.' -f1)
ref=../Reference/hs38DH.fasta
scatterdir=../Reference/ShortV_intervals
scatterlist=$(ls $scatterdir/*.list)
if [[ ${#scatterlist[@]} > 1 ]]; then
echo "$(date): ERROR - more than one scatter list file found: ${scatterlist[@]}"
exit
fi
bamdir=../Final_bams
out=../GATK4_HC
logs=./Logs/GATK4_HC
INPUTS=./Inputs
inputfile=${INPUTS}/gatk4_hc_missing.inputs
errs=./Logs/GATK4_HC_error_capture
rm -rf ${inputfile}
# Number of intervals
num_int=`wc -l ${scatterlist} | cut -d' ' -f 1`
# Collect sample IDs from samples.config
# Only collect IDs for germline variant calling (labids ending in -B)
while read -r sampleid labid seq_center library; do
if [[ ! -z ${sampleid} && ! ${sampleid} =~ ^#.*$ && ! ${labid} =~ -T.*$ && ! ${labid} =~ -P.*$ && ! ${labid} =~ -M.*$ ]]; then
samples+=("${labid}")
fi
done < "${config}"
echo "$(date): Checking GATK 4 HaplotypeCaller job for samples: ${#samples[@]}"
echo "$(date): Samples: ${samples[@]}"
# For each sample, check intervals with no .vcf and .vcf.idx files
for sample in "${samples[@]}"; do
# Check if .vcf and .vcf.idx files exist and are not empty
i=0
for interval in $(seq -f "%04g" 0 $((${num_int}-1))); do
logdir=${logs}/${sample}
errdir=${errs}/${sample}
logfile=${logdir}/${interval}.log
errfile=${errdir}/${sample}.${index}.err
outdir=${out}/${sample}
vcf=${outdir}/${sample}.${interval}.vcf
idx=${outdir}/${sample}.${interval}.vcf.idx
bam=${bamdir}/${sample}.final.bam
if ! [[ -s "${vcf}" && -s "${idx}" ]]; then
intfile=$(grep ${interval} ${scatterlist})
echo "${ref},${sample},${bam},${scatterdir}/${intfile},${outdir},${logdir},${errdir}" >> ${inputfile}
elif [ -s "${err}" ]; then
echo "$(date): Error detected. See $err and investigate. Writing task to input file"
intfile=$(grep ${interval} ${scatterlist})
echo "${ref},${sample},${bam},${scatterdir}/${intfile},${outdir},${logdir},${errdir}" >> ${inputfile}
else
((++i))
fi
done
if [[ $i == ${num_int} ]]; then
echo "$(date): ${sample} has all vcf and vcf.idx present. Ready for merging into GVCF."
else
num_missing=$((${num_int} - $i))
echo "$(date): ${sample} has ${num_missing} missing vcf or vcf.idx files."
total_missing=$((${total_missing}+${num_missing}))
fi
done
if [[ ${total_missing} ]]; then
echo "$(date): There are $total_missing vcf files in $config. Please run gatk4_hc_missing_run_parallel.pbs"
else
echo "$(date): Found all vcf and idx files for samples in $config."
fi