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callSvFromBam.sh
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#!/bin/bash
OPTSTRING="hr:s:i:o:t:c:l:b:"
usage()
{
echo -e "You did it wrong"
}
declare SWITCH
threads=8
bam_base="NONE"
ref="NONE"
getref="FALSE"
# Examine individual options
while getopts "$OPTSTRING" SWITCH; do
case $SWITCH in
r) ref="$OPTARG"
ref=$(readlink -e "$ref")
echo "Reference = $ref"
;;
s) settings="$OPTARG"
echo "Settings = $settings"
;;
i) fasta_dir="$OPTARG"
fasta_dir=$(readlink -e "$fasta_dir")
echo "Fasta Directory = $fasta_dir"
;;
b) bam_base="$OPTARG"
bam_base=$(readlink -e "$bam_base")
echo "Bam base Directory = $bam_base"
;;
o) out_dir="$OPTARG"
out_dir=$(readlink -e "$out_dir")
echo "Output directory = $out_dir"
;;
t) tools_dir="$OPTARG"
tools_dir=$(readlink -e "$tools_dir")
echo "Tools directory = $tools_dir"
;;
l) tools_list="$OPTARG"
declare -a tools=($tools_list)
echo "Going to run the following tools = $tools"
;;
c) threads="$OPTARG"
echo "Threads = $threads"
;;
*) echo "script error: unhandled argument"
usage
exit 1
;;
esac
done
source $tools_dir/log_eval.sh
SAMBAMBA="docker run -u 1001:1001 --name sambamba --rm -v $PWD:$PWD -w $PWD clinicalgenomics/sambamba:0.8.0"
#declare -a tools=("wham" "svaba" "pindel" "bdmax" "softsv" "manta" "lumpy" "delly_1.1.6" "gridss")
declare -a fractionOfReads=(100 75 50 25)
seed=87
# IF no reference was defined get it from path
if [ $ref = "NONE" ]; then
getref="TRUE"
fi
stamp="$(date +'%Y_%d_%m-%H_%M_%S')"
org="CBS7435"
grep -v '^#' $settings | while IFS=$'\t' read -r -a settings_array
do
base_in=$(basename "$fasta_dir")
settings_string="${settings_array[0]}_f${settings_array[1]}_l${settings_array[2]}_m${settings_array[3]}_s${settings_array[4]}"
if [ $bam_base = "NONE" ]; then
bamdir=$out_dir/${base_in/fasta/bam}/$settings_string
svsdir=$out_dir/${base_in/fasta/svs}/$settings_string
else
bamdir=$bam_base/$settings_string
svsdir=${bam_base/bam/svs}/$settings_string
fi
fastqdir=$out_dir/${base_in/fasta/fastq}/$settings_string
timing=${svsdir}/${stamp}_timing.tsv
log=${svsdir}/${stamp}_sv_calling.log
echo "THIS IS the DIRECTORY: $bamdir"
if [ ! -d $svsdir ]; then
mkdir -m 777 $svsdir
fi
touch $timing
touch $log
for dir in "$fasta_dir"/*; do
if [[ -d $dir ]]; then
base=$(basename "$dir")
if [ ! -d $svsdir/$base ]; then
mkdir -m 777 $svsdir/$base
fi
READ1_FILE="${fastqdir}/${base}_1.fq.gz"
READ2_FILE="${fastqdir}/${base}_2.fq.gz"
SAM="${bamdir}/${base}.sam"
BAM_SORTED="${bamdir}/${base}.sorted.bam"
if [ $getref = "TRUE" ]; then
ref=$bam_base/${base}_refPlasmid.fasta
fi
echo "╔══════════════════════════════════════════════════════════════╗"
echo "║ starting SV analysis ║"
echo "╚══════════════════════════════════════════════════════════════╝"
if [ -s "$BAM_SORTED" ]; then
for fraction in "${fractionOfReads[@]}"; do
BAM_FRACTION=$BAM_SORTED
if [ $fraction -ne 100 ]; then
BAM_FRACTION="${BAM_SORTED/.bam/-${fraction}.bam}"
log_eval $PWD "$SAMBAMBA sambamba view -h -t $threads -s 0.$fraction -f bam \
--subsampling-seed=$seed -o $BAM_FRACTION $BAM_SORTED"
fi
for tool in "${tools[@]}"; do
tool_outdir="$svsdir/$base/${tool}_${fraction}"
if [ ! -d "$tool_outdir" ]; then
mkdir -m 777 "$tool_outdir"
export -f log_eval
log_eval $PWD "$tools_dir/$tool/${tool}.sh $BAM_FRACTION $ref $READ1_FILE $READ2_FILE $tool_outdir $threads $tools_dir $timing" "$log"
fi
done
if [ $fraction -ne 100 ]; then
rm ${BAM_FRACTION}*
fi
done
fi
fi
done
done