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SNP_VQSR_INDEL_HF_SUBMITTER.sh
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SNP_VQSR_INDEL_HF_SUBMITTER.sh
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#! /bin/bash
###################
# INPUT VARIABLES #
###################
PROJECT_MS=$1 # the project where the multi-sample vcf is being written to
SAMPLE_SHEET=$2 # full/relative path to the sample sheet
PREFIX=$3 # prefix name that you want to give the multi-sample vcf
ARRAY_REF=$4 # OPTIONAL: if there is argument present the array reference genome is grch38. otherwise the default is grch37.
if
[[ ! ${ARRAY_REF} ]]
then
ARRAY_REF="grch37"
fi
SNP_SENSITIVITY=$5 # SNP TRUTH SENTIVITY CUT-OFF FOR VQSR (OPTIONAL). DEFAULT IS 99.5
# VALUE MUST HAVE ONE DECIMAL POINT (e.g. 99.7)
if
[[ ! ${SNP_SENSITIVITY} ]]
then
SNP_SENSITIVITY="99.5"
fi
PRIORITY=$6 # SGE PRIORITY. default is -14. range is -1 to -1023. CLOSER TO ZERO IS HIGHER PRIORITY.
# OPTIONAL: IF YOU WANT TO SET THIS YOU NEED TO SET SNP SENSIVITY AS WELL. EVEN TO THE DEFAULT VALUE.
if
[[ ! ${PRIORITY} ]]
then
PRIORITY="-14"
fi
NUMBER_OF_BED_FILES=$7 # scatter count. HOW MANY FILES YOU WANT TO BREAK UP THE BED FILE INTO FOR PARALLEL PROCESSING DISTRIBUTION.
# OPTIONAL: IF YOU WANT TO SET THIS YOU NEED TO SET SNP SENSITIVITY AS WELL AS SGE PRIORITY. EVEN TO THE DEFAULT VALUES.
if
[[ ! ${NUMBER_OF_BED_FILES} ]]
then
NUMBER_OF_BED_FILES=500
fi
###########################
# CORE VARIABLES/SETTINGS #
###########################
# CHANGE SCRIPT DIR TO WHERE YOU HAVE HAVE THE SCRIPTS BEING SUBMITTED
SUBMITTER_SCRIPT_PATH=$( cd "$(dirname "${BASH_SOURCE[0]}")" ; pwd -P )
SCRIPT_DIR="${SUBMITTER_SCRIPT_PATH}/SNP_VQSR_INDEL_HF"
COMMON_SCRIPT_DIR="${SUBMITTER_SCRIPT_PATH}/COMMON_SCRIPTS"
COMMON_VQSR_SCRIPT_DIR="${SUBMITTER_SCRIPT_PATH}/COMMON_VQSR_SCRIPTS"
COMMON_GRCH37_SCRIPT_DIR="${SUBMITTER_SCRIPT_PATH}/COMMON_GRCH37_SCRIPTS"
COMMON_HARD_FILTER_SCRIPT_DIR="${SUBMITTER_SCRIPT_PATH}/COMMON_HARD_FILTER_SCRIPTS"
# gcc is so that it can be pushed out to the compute nodes via qsub (-V)
module load gcc/7.2.0
# Directory where sequencing projects are located
CORE_PATH="/mnt/research/active"
# Generate a list of active queue and remove the ones that I don't want to use
QUEUE_LIST=$(qstat -f -s r \
| egrep -v "^[0-9]|^-|^queue|^ " \
| cut -d @ -f 1 \
| sort \
| uniq \
| egrep -v "bigmem.q|all.q|cgc.q|programmers.q|rhel7.q|qtest.q|bigdata.q|uhoh.q|testcgc.q" \
| datamash collapse 1 \
| awk '{print $1}')
# | awk '{print $1,"-l \x27hostname=!DellR730-03\x27"}'`
# eventually, i want to push this out to something...maybe in the vcf file header.
PIPELINE_VERSION=$(git \
--git-dir=${SCRIPT_DIR}/../.git \
--work-tree=${SCRIPT_DIR}/.. \
log \
--pretty=format:'%h' \
-n 1)
# generate a random number b/w "0 - 32767" to be used for the job name for variant annotator both pre and post refinement
# this is to help cut down on the job name length so I can increase the scatter count
HACK=$(echo ${RANDOM})
# explicitly setting this b/c not everybody has had the $HOME directory transferred and I'm not going to through
# and figure out who does and does not have this set correctly
umask 0007
# grab email addy
SEND_TO=$(cat ${SCRIPT_DIR}/../email_lists.txt)
# make a directory to place the annovar logs
ANNOVAR_LOGS="/mnt/research/tools/LOGS"
mkdir -p ${ANNOVAR_LOGS}
# QSUB ARGUMENTS LIST
# set shell on compute node
# start in current working directory
# transfer submit node env to compute node
# set SINGULARITY BINDPATH
# set queues to submit to
# set priority
# combine stdout and stderr logging to same output file
QSUB_ARGS="-S /bin/bash" \
QSUB_ARGS=${QSUB_ARGS}" -cwd" \
QSUB_ARGS=${QSUB_ARGS}" -V" \
QSUB_ARGS=${QSUB_ARGS}" -v SINGULARITY_BINDPATH=/mnt:/mnt" \
QSUB_ARGS=${QSUB_ARGS}" -q ${QUEUE_LIST}" \
QSUB_ARGS=${QSUB_ARGS}" -p ${PRIORITY}" \
QSUB_ARGS=${QSUB_ARGS}" -j y"
#####################
# PIPELINE PROGRAMS #
#####################
JAVA_1_8="/mnt/linuxtools/JAVA/jdk1.8.0_73/bin"
BEDTOOLS_DIR="/mnt/linuxtools/BEDTOOLS/bedtools-2.22.0/bin"
GATK_DIR="/mnt/linuxtools/GATK/GenomeAnalysisTK-3.7"
SAMTOOLS_0118_DIR="/mnt/linuxtools/SAMTOOLS/samtools-0.1.18"
# Becasue I didn't want to go through compiling this yet for version 1.6...I'm hoping that Keith will eventually do a full OS install of RHEL7 instead of his
# typical stripped down installations so I don't have to install multiple libraries again
TABIX_DIR="/mnt/linuxtools/TABIX/tabix-0.2.6"
CIDRSEQSUITE_JAVA_DIR="/mnt/linuxtools/JAVA/jre1.7.0_45/bin"
CIDRSEQSUITE_6_1_1_DIR="/mnt/linuxtools/CIDRSEQSUITE/6.1.1"
CIDRSEQSUITE_ANNOVAR_JAVA="/mnt/linuxtools/JAVA/jre1.6.0_25/bin"
CIDRSEQSUITE_DIR_4_0="/mnt/research/tools/LINUX/CIDRSEQSUITE/Version_4_0"
CIDRSEQSUITE_PROPS_DIR="/mnt/research/tools/LINUX/00_GIT_REPO_KURT/CIDR_SEQ_CAPTURE_JOINT_CALL/STD_VQSR"
# cp -p /u01/home/hling/cidrseqsuite.props.HGMD /mnt/research/tools/LINUX/00_GIT_REPO_KURT/CIDR_SEQ_CAPTURE_JOINT_CALL/STD_VQSR/cidrseqsuite.props
# 14 June 2018
CIDRSEQSUITE_7_5_0_DIR="/mnt/research/tools/LINUX/CIDRSEQSUITE/7.5.0"
LAB_QC_DIR="/mnt/linuxtools/CUSTOM_CIDR/EnhancedSequencingQCReport/0.1.1"
# Copied from /mnt/research/tools/LINUX/CIDRSEQSUITE/pipeline_dependencies/QC_REPORT/EnhancedSequencingQCReport.jar
# md5 f979bb4dc8d97113735ef17acd3a766e EnhancedSequencingQCReport.jar
SAMTOOLS_DIR="/mnt/linuxtools/ANACONDA/anaconda2-5.0.0.1/bin"
# This is samtools version 1.7
# I have no idea why other users other than me cannot index a cram file with a version of samtools that I built from the source
# Apparently the version that I built with Anaconda works for other users, but it performs REF_CACHE first...
DATAMASH_DIR="/mnt/research/tools/LINUX/DATAMASH/datamash-1.0.6"
TABIX_DIR="/mnt/research/tools/LINUX/TABIX/tabix-0.2.6"
R_DIRECTORY="/mnt/linuxtools/R/R-3.1.1/bin"
GATK_DIR_4011="/mnt/linuxtools/GATK/gatk-4.0.11.0"
PICARD_DIR="/mnt/linuxtools/PICARD/picard-2.20.6"
PARALLEL_DIR="/cm/shared/apps/parallel/20161222/bin"
PICARD_LIFTOVER_CONTAINER="/mnt/research/tools/LINUX/00_GIT_REPO_KURT/CONTAINERS/picard-2.26.10.0.simg"
ALIGNMENT_CONTAINER="/mnt/research/tools/LINUX/00_GIT_REPO_KURT/CONTAINERS/ddl_ce_control_align-0.0.5.simg"
##################
# PIPELINE FILES #
##################
HAPMAP_VCF="/mnt/research/tools/PIPELINE_FILES/GATK_resource_bundle/2.8/b37/hapmap_3.3.b37.vcf"
OMNI_VCF="/mnt/research/tools/PIPELINE_FILES/GATK_resource_bundle/2.8/b37/1000G_omni2.5.b37.vcf"
ONEKG_SNPS_VCF="/mnt/research/tools/PIPELINE_FILES/GATK_resource_bundle/2.8/b37/1000G_phase1.snps.high_confidence.b37.vcf"
DBSNP_138_VCF="/mnt/research/tools/PIPELINE_FILES/GATK_resource_bundle/2.8/b37/dbsnp_138.b37.vcf"
ONEKG_INDELS_VCF="/mnt/research/tools/PIPELINE_FILES/GATK_resource_bundle/2.8/b37/Mills_and_1000G_gold_standard.indels.b37.vcf"
P3_1KG="/mnt/research/tools/PIPELINE_FILES/GRCh37_aux_files/ALL.wgs.phase3_shapeit2_mvncall_integrated_v5.20130502.sites.vcf.gz"
ExAC="/mnt/research/tools/PIPELINE_FILES/GRCh37_aux_files/ExAC.r0.3.sites.vep.vcf.gz"
KNOWN_SNPS="/mnt/research/tools/PIPELINE_FILES/GATK_resource_bundle/2.8/b37/dbsnp_138.b37.excluding_sites_after_129.vcf"
VERACODE_CSV="/mnt/linuxtools/CIDRSEQSUITE/Veracode_hg18_hg19.csv"
B37_TO_HG19_CHAIN="/mnt/shared_resources/public_resources/liftOver_chain/chainFiles_b37/b37tohg19.chain"
HG19_REF="/mnt/research/tools/PIPELINE_FILES/GATK_resource_bundle/2.8/hg19/ucsc.hg19.fasta"
HG19_TO_GRCH38_CHAIN="/mnt/shared_resources/public_resources/liftOver_chain/hg19ToHg38.over.chain"
GRCH38_REF="/mnt/research/tools/PIPELINE_FILES/GRCh38_aux_files/Homo_sapiens_assembly38.fasta"
REF_DICT="/mnt/research/tools/PIPELINE_FILES/bwa_mem_0.7.5a_ref/human_g1k_v37_decoy.dict"
# what is used in the clinical exome pipeline line...at least at first. basically longest transcript per translated gene
REF_SEQ_TRANSCRIPTS="/mnt/research/tools/PIPELINE_FILES/GRCh37_aux_files/RefSeq.Unique.GRCh37.FINAL.19Feb2018.bed"
##################################################
##################################################
##### JOINT CALLING PROJECT SET-UP ###############
### WHERE THE MULTI-SAMPLE VCF GETS WRITTEN TO ###
##################################################
##################################################
# This checks to see if bed file directory and split gvcf list has been created from a previous run.
# If so, remove them to not interfere with current run
if
[ -d ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT ]
then
rm -rf ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT
fi
if
[ -d ${CORE_PATH}/${PROJECT_MS}/TEMP/SPLIT_LIST ]
then
rm -rf ${CORE_PATH}/${PROJECT_MS}/TEMP/SPLIT_LIST
fi
############################################################################################
##### MAKE THE FOLLOWING FOLDERS IN THE PROJECT WHERE THE MULTI-SAMPLE VCF IS GOING TO #####
############################################################################################
mkdir -p ${CORE_PATH}/${PROJECT_MS}/{LOGS,COMMAND_LINES}
mkdir -p ${CORE_PATH}/${PROJECT_MS}/TEMP/{BED_FILE_SPLIT,AGGREGATE,QC_REPORT_PREP_${PREFIX},SPLIT_LIST}
mkdir -p ${CORE_PATH}/${PROJECT_MS}/MULTI_SAMPLE/VARIANT_SUMMARY_STAT_VCF/
mkdir -p ${CORE_PATH}/${PROJECT_MS}/GVCF/AGGREGATE
mkdir -p ${CORE_PATH}/${PROJECT_MS}/REPORTS/{ANNOVAR,LAB_PREP_REPORTS_MS,QC_REPORTS}
mkdir -p ${CORE_PATH}/${PROJECT_MS}/REPORTS/QC_REPORT_PREP_MS/QC_REPORT_PREP_${PREFIX}
mkdir -p ${CORE_PATH}/${PROJECT_MS}/REPORTS/VCF_METRICS/MULTI_SAMPLE/
mkdir -p ${CORE_PATH}/${PROJECT_MS}/TEMP/ANNOVAR/${PREFIX}
mkdir -p ${CORE_PATH}/${PROJECT_MS}/LOGS/{A01_COMBINE_GVCF,B01_GENOTYPE_GVCF,C01_VARIANT_ANNOTATOR,H01_CALCULATE_GENOTYPE_POSTERIORS,I01_VARIANT_ANNOTATOR_REFINED}
mkdir -p ${CORE_PATH}/${PROJECT_MS}/LOGS/{G01A01_LIFTOVER_INITIAL_MS_TO_HG19,G01A01A01_LIFTOVER_INITIAL_HG19_TO_HG38,I02_LIFTOVER_HG19_REFINED,I02A01_LIFTOVER_GRCH38_REFINED}
##################################################
### FUNCTIONS FOR JOINT CALLING PROJECT SET-UP ###
##################################################
# grab the reference genome file, dbsnp file and bait bed file for the "project"
## !should do a check here to make sure that there is only one record...!
CREATE_PROJECT_INFO_ARRAY ()
{
PROJECT_INFO_ARRAY=(`sed 's/\r//g' ${SAMPLE_SHEET} \
| awk 'BEGIN{FS=","} NR>1 {print $12,$15,$16,$17,$18}' \
| sed 's/,/\t/g' \
| sort -k 1,1 \
| awk '{print $1,$2,$3,$4,$5}' \
| sort \
| uniq`)
REF_GENOME=${PROJECT_INFO_ARRAY[0]} # field 12 from the sample sheet
PROJECT_TITV_BED=${PROJECT_INFO_ARRAY[1]} # field 15 from the sample sheet
PROJECT_TITV_BED_NAME=$(basename ${PROJECT_TITV_BED} .bed)
PROJECT_BAIT_BED=${PROJECT_INFO_ARRAY[2]} # field 16 from the sample sheet
PROJECT_TARGET_BED=${PROJECT_INFO_ARRAY[3]} # field 17 from the sample sheet
PROJECT_TARGET_BED_NAME=$(basename ${PROJECT_TARGET_BED} .bed)
PROJECT_DBSNP=${PROJECT_INFO_ARRAY[4]} # field 18 from the sample sheet
}
# GET RID OF ALL THE COMMON BED FILE EFF-UPS,
FORMAT_AND_SCATTER_BAIT_BED ()
{
BED_FILE_PREFIX=$(echo BF)
# make sure that there is EOF
# remove CARRIAGE RETURNS
# remove CHR PREFIXES (THIS IS FOR GRCH37)
# CONVERT VARIABLE LENGTH WHITESPACE FIELD DELIMETERS TO SINGLE TAB.
awk 1 ${PROJECT_BAIT_BED} | sed -r 's/\r//g ; s/chr//g ; s/[[:space:]]+/\t/g' \
>| ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/FORMATTED_BED_FILE.bed
# SORT TO GRCH37 ORDER
# DO NOT ADD MT
(awk '$1~/^[0-9]/' ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/FORMATTED_BED_FILE.bed | sort -k1,1n -k2,2n ; \
awk '$1=="X"' ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/FORMATTED_BED_FILE.bed | sort -k 2,2n ; \
awk '$1=="Y"' ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/FORMATTED_BED_FILE.bed | sort -k 2,2n) \
>| ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/FORMATTED_AND_SORTED_BED_FILE.bed
# Determining how many records will be in each mini-bed file.
# The +1 at the end is to round up the number of records per mini-bed file to ensure all records are captured.
# So the last mini-bed file will be smaller.
# IIRC. this statement isn't really true, but I don't feel like figuring it out right now. KNH
INTERVALS_DIVIDED=$(wc -l ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/FORMATTED_AND_SORTED_BED_FILE.bed \
| awk '{print $1"/""'${NUMBER_OF_BED_FILES}'"}' \
| bc \
| awk '{print $0+1}')
split -l ${INTERVALS_DIVIDED} \
-a 4 \
-d \
${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/FORMATTED_AND_SORTED_BED_FILE.bed \
${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/$BED_FILE_PREFIX
# ADD A .bed suffix to all of the now splitted files
ls ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/$BED_FILE_PREFIX* \
| awk '{print "mv",$0,$0".bed"}' \
| bash
# fix target and ti/tv bed files
# make sure that there is EOF
# remove CARRIAGE RETURNS
# remove CHR PREFIXES (THIS IS FOR GRCH37)
# CONVERT VARIABLE LENGTH WHITESPACE FIELD DELIMETERS TO SINGLE TAB.
awk 1 ${PROJECT_TARGET_BED} \
| sed -r 's/\r//g ; s/chr//g ; s/[[:space:]]+/\t/g' \
>| ${CORE_PATH}/${PROJECT_MS}/TEMP/${PROJECT_MS}-${PROJECT_TARGET_BED_NAME}.bed
awk 1 ${PROJECT_TITV_BED} \
| sed -r 's/\r//g ; s/chr//g ; s/[[:space:]]+/\t/g' \
>| ${CORE_PATH}/${PROJECT_MS}/TEMP/${PROJECT_MS}-${PROJECT_TITV_BED_NAME}.bed
# convert fixed bed files into picard interval lists
(grep "^@SQ" ${REF_DICT} \
; awk 'BEGIN {OFS="\t"} \
{print $1,($2+1),$3,"+",$1"_"($2+1)"_"$3}' \
${CORE_PATH}/${PROJECT_MS}/TEMP/${PROJECT_MS}-${PROJECT_TARGET_BED_NAME}.bed) \
>| ${CORE_PATH}/${PROJECT_MS}/TEMP/${PROJECT_MS}-${PROJECT_TARGET_BED_NAME}-picard.bed
(grep "^@SQ" ${REF_DICT} \
; awk 'BEGIN {OFS="\t"} \
{print $1,($2+1),$3,"+",$1"_"($2+1)"_"$3}' \
${CORE_PATH}/${PROJECT_MS}/TEMP/${PROJECT_MS}-${PROJECT_TITV_BED_NAME}.bed) \
>| ${CORE_PATH}/${PROJECT_MS}/TEMP/${PROJECT_MS}-${PROJECT_TITV_BED_NAME}-picard.bed
}
##########################################################################################################
##### UNIQUE THE SAMPLE INTO SAMPLE/PROJECT COMBOS AND CREATE A SAMPLE SHEET INTO 300 SAMPLE CHUNKS. #####
##########################################################################################################
### god, i was really tired and under a lot of pressure when I did this...i've done it more sensibly in ##
### other pipelines since then, but if this still works I'm not going to rework it to match what I did ###
### in the other pipelines ###
##############################
awk 'BEGIN {FS=",";OFS="\t"} NR>1 {print $1,$8}' \
${SAMPLE_SHEET} \
| sort -k 1,1 -k 2,2 \
| uniq \
| split -l 300 -a 4 -d - \
${CORE_PATH}/${PROJECT_MS}/TEMP/SPLIT_LIST/
# # Use the chunked up sample sheets to create gvcf list chunks
for PROJECT_SAMPLE_LISTS in \
$(ls ${CORE_PATH}/${PROJECT_MS}/TEMP/SPLIT_LIST/*)
do
awk 'BEGIN {OFS="/"} {print "'${CORE_PATH}'",$1,"GVCF",$2".g.vcf.gz"}' \
${PROJECT_SAMPLE_LISTS} \
>| ${PROJECT_SAMPLE_LISTS}.list
done
# take all of the project/sample combos in the sample sheet and write a g.vcf file path to a *list file
# At this point this is just for record keeping...it is being scatterred above
CREATE_GVCF_LIST ()
{
# count how many unique sample id's (with project) are in the sample sheet.
TOTAL_SAMPLES=$(awk 'BEGIN{FS=","} NR>1{print $1,$8}' ${SAMPLE_SHEET} \
| sort \
| uniq \
| wc -l)
# find all of the gvcf files write all of the full paths to a *samples.gvcf.list file.
awk 'BEGIN{FS=","} NR>1{print $1,$8}' ${SAMPLE_SHEET} \
| sort \
| uniq \
| awk 'BEGIN{OFS="/"}{print "ls " "'${CORE_PATH}'",$1,"GVCF",$2".g.vcf*"}' \
| bash \
| egrep -v "idx|tbi|md5" \
>| ${CORE_PATH}/${PROJECT_MS}/${TOTAL_SAMPLES}.samples.gvcf.list
# STORE THE GVCF LIST FILE PATH AS A VARIABLE
GVCF_LIST=$(echo ${CORE_PATH}/${PROJECT_MS}/${TOTAL_SAMPLES}.samples.gvcf.list)
}
# Run Ben's EnhancedSequencingQCReport which;
# Generates a QC report for lab specific metrics including Physique Report, Samples Table, Sequencer XML data, Pca and Phoenix.
# Does not check if samples are dropped.
RUN_LAB_PREP_METRICS ()
{
echo \
qsub \
${QSUB_ARGS} \
-N A02-LAB_PREP_METRICS_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/${PROJECT_MS}-LAB_PREP_METRICS.log \
${COMMON_SCRIPT_DIR}/A02_LAB_PREP_METRICS.sh \
${JAVA_1_8} \
${LAB_QC_DIR} \
${CORE_PATH} \
${PROJECT_MS} \
${SAMPLE_SHEET}
}
############################################################
##### CALL THE ABOVE FUNCTIONS TO SET-UP JOINT CALLING #####
############################################################
CREATE_PROJECT_INFO_ARRAY
FORMAT_AND_SCATTER_BAIT_BED
CREATE_GVCF_LIST
RUN_LAB_PREP_METRICS
echo sleep 0.1s
#################################################################
##### CREATE SAMPLE SPECIFIC SUB-DIRECTORIES, FIX BED FILES #####
#################################################################
# for each unique sample id in the sample sheet grab the bed files, ref genome, project and store as an array
CREATE_SAMPLE_INFO_ARRAY ()
{
SAMPLE_INFO_ARRAY=(`sed 's/\r//g' ${SAMPLE_SHEET} \
| awk 'BEGIN{FS=","} NR>1 {print $1,$8,$16,$17,$15,$18,$12}' \
| sed 's/,/\t/g' \
| sort -k 2,2 \
| uniq \
| awk '$2=="'${SAMPLE}'" {print $1,$2,$3,$4,$5,$6,$7,NR}'`)
PROJECT_SAMPLE=${SAMPLE_INFO_ARRAY[0]}
SM_TAG=${SAMPLE_INFO_ARRAY[1]}
BAIT_BED=${SAMPLE_INFO_ARRAY[2]}
TARGET_BED=${SAMPLE_INFO_ARRAY[3]}
TITV_BED=${SAMPLE_INFO_ARRAY[4]}
DBSNP=${SAMPLE_INFO_ARRAY[5]} #Not used unless we implement HC_BAM
SAMPLE_REF_GENOME=${SAMPLE_INFO_ARRAY[6]}
SAMPLE_ROW_COUNT=${SAMPLE_INFO_ARRAY[7]}
UNIQUE_ID_SM_TAG=$(echo ${SM_TAG} | sed 's/@/_/g') # If there is an @ in the qsub or holdId name it breaks
BARCODE_2D=$(echo ${SM_TAG} | awk '{split($1,SM_TAG,/[@-]/); print SM_TAG[2]}') # SM_TAG = RIS_ID[@-]BARCODE_2D
}
# for each sample make a bunch directories if not already present in the samples defined project directory
MAKE_PROJ_DIR_TREE ()
{
mkdir -p \
${CORE_PATH}/$PROJECT_SAMPLE/{TEMP,LOGS,COMMAND_LINES} \
${CORE_PATH}/$PROJECT_SAMPLE/REPORTS/CONCORDANCE_MS \
${CORE_PATH}/${PROJECT_MS}/TEMP/${SM_TAG} \
${CORE_PATH}/${PROJECT_MS}/LOGS/${SM_TAG}
}
###################################################
### fix common formatting problems in bed files ###
### create picard style interval files ############
### DO PER SAMPLE #################################
###################################################
FIX_BED_FILES ()
{
echo \
qsub \
${QSUB_ARGS} \
-N A00-FIX_BED_FILES_${UNIQUE_ID_SM_TAG}_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_SAMPLE}/LOGS/${SM_TAG}/${SM_TAG}-FIX_BED_FILES.log \
${COMMON_GRCH37_SCRIPT_DIR}/A00-FIX_BED_FILES.sh \
${CORE_PATH} \
${ALIGNMENT_CONTAINER} \
${PROJECT_MS} \
${SM_TAG} \
${BAIT_BED} \
${TARGET_BED} \
${TITV_BED} \
${REF_DICT} \
${B37_TO_HG19_CHAIN} \
${HG19_TO_GRCH38_CHAIN}
}
for SAMPLE in \
$(awk 'BEGIN {FS=","} NR>1 {print $8}' ${SAMPLE_SHEET} \
| sort \
| uniq )
do
CREATE_SAMPLE_INFO_ARRAY
MAKE_PROJ_DIR_TREE
FIX_BED_FILES
echo sleep 0.1s
done
#######################################################################
#######################################################################
################# Scatter of Joint Calling ############################
#######################################################################
#######################################################################
# aggregate all of individual g.vcf into one cohort g.vcf per bed file chunk
COMBINE_GVCF ()
{
echo \
qsub \
${QSUB_ARGS} \
-N A01_COMBINE_GVCF_${PROJECT_MS}_${PGVCF_LIST_NAME}_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/A01_COMBINE_GVCF/A01_COMBINE_GVCF_${PGVCF_LIST_NAME}_${BED_FILE_NAME}.log \
${COMMON_SCRIPT_DIR}/A01_COMBINE_GVCF.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PGVCF_LIST} \
${PREFIX} \
${BED_FILE_NAME}
}
for BED_FILE in \
$(ls ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/BF*bed);
do
BED_FILE_NAME=$(basename ${BED_FILE} .bed)
for PGVCF_LIST in \
$(ls ${CORE_PATH}/${PROJECT_MS}/TEMP/SPLIT_LIST/*list)
do
PGVCF_LIST_NAME=$(basename ${PGVCF_LIST} .list)
COMBINE_GVCF
echo sleep 0.1s
done
done
#####################################################################
BUILD_HOLD_ID_GENOTYPE_GVCF ()
{
for PROJECT_A in ${PROJECT_MS};
# yeah, so uh, this looks bad, but I just needed a way to set a new project variable that equals the multi-sample project variable.
do
GENOTYPE_GVCF_HOLD_ID="-hold_jid "
for PGVCF_LIST in \
$(ls ${CORE_PATH}/$PROJECT_A/TEMP/SPLIT_LIST/*list)
do
PGVCF_LIST_NAME=$(basename ${PGVCF_LIST} .list)
GENOTYPE_GVCF_HOLD_ID=${GENOTYPE_GVCF_HOLD_ID}A01_COMBINE_GVCF_${PROJECT_A}_${PGVCF_LIST_NAME}_${BED_FILE_NAME},
done
done
}
# genotype the cohort g.vcf chunks
GENOTYPE_GVCF ()
{
echo \
qsub \
${QSUB_ARGS} \
-N B01_GENOTYPE_GVCF_${PROJECT_MS}_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/B01_GENOTYPE_GVCF/B01_GENOTYPE_GVCF_${BED_FILE_NAME}.log \
${GENOTYPE_GVCF_HOLD_ID} \
${COMMON_SCRIPT_DIR}/B01_GENOTYPE_GVCF.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${BED_FILE_NAME}
}
# add dnsnp ID, genotype summaries, gc percentage, variant class, tandem repeat units and homopolymer runs to genotyped g.vcf chunks.
VARIANT_ANNOTATOR ()
{
echo \
qsub \
${QSUB_ARGS} \
-N C${HACK}_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/C01_VARIANT_ANNOTATOR/C01_VARIANT_ANNOTATOR_${BED_FILE_NAME}.log \
-hold_jid B01_GENOTYPE_GVCF_${PROJECT_MS}_${BED_FILE_NAME} \
${COMMON_SCRIPT_DIR}/C01_VARIANT_ANNOTATOR.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${BED_FILE_NAME} \
${PROJECT_DBSNP}
}
# build a string of job names (comma delim) from the variant annotator scatter to store as variable to use as
# hold_jid for the cat variants gather (it's used in the next section after the for loop below)
GENERATE_CAT_VARIANTS_HOLD_ID ()
{
CAT_VARIANTS_HOLD_ID=${CAT_VARIANTS_HOLD_ID}C${HACK}_${BED_FILE_NAME},
}
# for each chunk of the original bed file, do combine gvcfs, then genotype gvcfs, then variant annotator
# then generate a string of all the variant annotator job names submitted
for BED_FILE in \
$(ls ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/BF*bed);
do
BED_FILE_NAME=$(basename ${BED_FILE} .bed)
BUILD_HOLD_ID_GENOTYPE_GVCF
GENOTYPE_GVCF
echo sleep 0.1s
VARIANT_ANNOTATOR
echo sleep 0.1s
GENERATE_CAT_VARIANTS_HOLD_ID
done
#########################################################
#########################################################
##### VCF Gather and Genotype Refinement Functions #####
#########################################################
#########################################################
# use cat variants to gather up all of the vcf files above into one big file
# MIGHT WANT TO LOOK INTO GatherVcfs (Picard) here
# Other possibility is MergeVcfs (Picard)...GatherVcfs is supposedly used for scatter operations so hopefully more efficient
# The way that CatVariants is constructed, I think would cause a upper limit to the scatter operation.
CAT_VARIANTS ()
{
echo \
qsub \
${QSUB_ARGS} \
-N D01_CAT_VARIANTS_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/D01_CAT_VARIANTS.log \
-hold_jid ${CAT_VARIANTS_HOLD_ID} \
${COMMON_SCRIPT_DIR}/D01_CAT_VARIANTS.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# Breakout the snps
EXTRACT_SNV ()
{
echo \
qsub \
${QSUB_ARGS} \
-N E01_EXTRACT_SNV_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/E01_EXTRACT_SNV.log \
-hold_jid D01_CAT_VARIANTS_${PROJECT_MS} \
${COMMON_HARD_FILTER_SCRIPT_DIR}/E01_EXTRACT_SNV.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# run the snp vqsr model
VARIANT_RECALIBRATOR_SNV ()
{
echo \
qsub \
${QSUB_ARGS} \
-N E01-A01_VARIANT_RECALIBRATOR_SNV_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/E01-A01_VARIANT_RECALIBRATOR_SNV.log \
-hold_jid E01_EXTRACT_SNV_${PROJECT_MS} \
$SCRIPT_DIR/E01-A01_VARIANT_RECALIBRATOR_SNV.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${HAPMAP_VCF} \
${OMNI_VCF} \
${ONEKG_SNPS_VCF} \
${DBSNP_138_VCF} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${R_DIRECTORY} \
${SEND_TO}
}
# apply the snp vqsr model to the full vcf
APPLY_RECALIBRATION_SNV ()
{
echo \
qsub \
${QSUB_ARGS} \
-N E01-A01-A01_APPLY_RECALIBRATION_SNV_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/E01-A01-A01_APPLY_RECALIBRATION_SNV.log \
-hold_jid E01-A01_VARIANT_RECALIBRATOR_SNV_${PROJECT_MS} \
$SCRIPT_DIR/E01-A01-A01_APPLY_RECALIBRATION_SNV.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${SNP_SENSITIVITY}
}
# Breakout the non-snps
EXTRACT_INDEL_AND_MIXED ()
{
echo \
qsub \
${QSUB_ARGS} \
-N E02_EXTRACT_INDEL_AND_MIXED_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/E02_EXTRACT_INDEL_AND_MIXED.log \
-hold_jid D01_CAT_VARIANTS_${PROJECT_MS} \
${COMMON_HARD_FILTER_SCRIPT_DIR}/E02_EXTRACT_INDELS_AND_MIXED.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# Apply Hard Filters to Indels and Mixed
HARD_FILTER_INDEL_AND_MIXED ()
{
echo \
qsub \
${QSUB_ARGS} \
-N E02-A01_FILTER_INDEL_AND_MIXED_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/E02-A01_FILTER_INDEL_AND_MIXED.log \
-hold_jid E02_EXTRACT_INDEL_AND_MIXED_${PROJECT_MS} \
${COMMON_HARD_FILTER_SCRIPT_DIR}/E02-A01_FILTER_INDELS_AND_MIXED.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# COMBINE_VARIANTS
COMBINE_SNV_INDEL_VARIANTS ()
{
echo \
qsub \
${QSUB_ARGS} \
-N F01_COMBINE_VARIANTS_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/F01_COMBINE_VARIANTS.log \
-hold_jid E01-A01-A01_APPLY_RECALIBRATION_SNV_${PROJECT_MS},E02-A01_FILTER_INDEL_AND_MIXED_${PROJECT_MS} \
${COMMON_HARD_FILTER_SCRIPT_DIR}/F01_COMBINE_VARIANTS.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# call cat variants and vqsr
CAT_VARIANTS
echo sleep 0.1s
EXTRACT_SNV
echo sleep 0.1s
VARIANT_RECALIBRATOR_SNV
echo sleep 0.1s
APPLY_RECALIBRATION_SNV
echo sleep 0.1s
EXTRACT_INDEL_AND_MIXED
echo sleep 0.1s
HARD_FILTER_INDEL_AND_MIXED
echo sleep 0.1s
COMBINE_SNV_INDEL_VARIANTS
echo sleep 0.1s
##################################################
##################################################
##### SCATTER FOR GENOTYPE REFINEMENT ############
##################################################
##################################################
# liftover initial final vcf to hg19
LIFTOVER_INITIAL_GRCH37_VCF_TO_HG19 ()
{
echo \
qsub \
${QSUB_ARGS} \
-N G01A01_LIFTOVER_INITIAL_GRCH37_TO_HG19_${PROJECT_MS}_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/G01A01_LIFTOVER_INITIAL_MS_TO_HG19/G01A01_LIFTOVER_INITIAL_MS_TO_HG19_${BED_FILE_NAME}.log \
-hold_jid F01_COMBINE_VARIANTS_${PROJECT_MS} \
${COMMON_GRCH37_SCRIPT_DIR}/G01A01_LIFTOVER_INITIAL_GRCH37_TO_HG19.sh \
${JAVA_1_8} \
${PICARD_DIR} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${HG19_REF} \
${B37_TO_HG19_CHAIN} \
${BED_FILE_NAME}
}
# liftover initial hg19 vcf to grch38
LIFTOVER_INITIAL_HG19_VCF_TO_HG38 ()
{
echo \
qsub \
${QSUB_ARGS} \
-N I${HACK}L_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/G01A01A01_LIFTOVER_INITIAL_HG19_TO_HG38/G01A01A01_LIFTOVER_INITIAL_HG19_TO_HG38_${BED_FILE_NAME}.log \
-hold_jid G01A01_LIFTOVER_INITIAL_GRCH37_TO_HG19_${PROJECT_MS}_${BED_FILE_NAME} \
${COMMON_GRCH37_SCRIPT_DIR}/G01A01A01_LIFTOVER_INITIAL_HG19_TO_GRCH38.sh \
${JAVA_1_8} \
${PICARD_DIR} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${GRCH38_REF} \
${HG19_TO_GRCH38_CHAIN} \
${BED_FILE_NAME}
}
# do a scatter of genotype refinement using the same chunked bed files use to the g.vcf aggregation
# external priors used are the final 1kg genomes dataset, exac v0.3, no family priors used (no ped file)
CALCULATE_GENOTYPE_POSTERIORS ()
{
echo \
qsub \
${QSUB_ARGS} \
-N H01_CALCULATE_GENOTYPE_POSTERIORS_${PROJECT_MS}_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/H01_CALCULATE_GENOTYPE_POSTERIORS/H01_CALCULATE_GENOTYPE_POSTERIORS_${BED_FILE_NAME}.log \
-hold_jid F01_COMBINE_VARIANTS_${PROJECT_MS} \
${COMMON_SCRIPT_DIR}/H01_CALCULATE_GENOTYPE_POSTERIORS.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${P3_1KG} \
${ExAC} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${BED_FILE_NAME}
}
# recalculate the genotype summaries for the now refined genotypes for each vcf chunk
VARIANT_ANNOTATOR_REFINED ()
{
echo \
qsub \
${QSUB_ARGS} \
-N I${HACK}_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/I01_VARIANT_ANNOTATOR_REFINED/I01_VARIANT_ANNOTATOR_REFINED_${BED_FILE_NAME}.log \
-hold_jid H01_CALCULATE_GENOTYPE_POSTERIORS_${PROJECT_MS}_${BED_FILE_NAME} \
${COMMON_SCRIPT_DIR}/I01_VARIANT_ANNOTATOR_REFINED.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${PROJECT_DBSNP} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${BED_FILE_NAME}
}
# liftover refined genotypes to hg19
LIFTOVER_GRCH37_TO_HG19_REFINED_ANNOTATED ()
{
echo \
qsub \
${QSUB_ARGS} \
-N I${HACK}J_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/I02_LIFTOVER_HG19_REFINED/I02_LIFTOVER_HG19_REFINED_${BED_FILE_NAME}.log \
-hold_jid I${HACK}_${BED_FILE_NAME} \
${COMMON_GRCH37_SCRIPT_DIR}/I02_REFINED_LIFTOVER_VARIANTS_GRCH37_TO_HG19.sh \
${PICARD_LIFTOVER_CONTAINER} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${BED_FILE_NAME} \
${HG19_REF} \
${B37_TO_HG19_CHAIN} \
${SAMPLE_SHEET} \
${SUBMIT_STAMP}
}
# liftover refined genotypes from hg19 to grch38
LIFTOVER_HG19_TO_GRCH38_REFINED_ANNOTATED ()
{
echo \
qsub \
${QSUB_ARGS} \
-N I${HACK}K_${BED_FILE_NAME} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/I02A01_LIFTOVER_GRCH38_REFINED/I02A01_LIFTOVER_GRCH38_REFINED_${BED_FILE_NAME}.log \
-hold_jid I${HACK}J_${BED_FILE_NAME} \
${COMMON_GRCH37_SCRIPT_DIR}/I02A01_REFINED_LIFTOVER_VARIANTS_HG19_TO_GRCH38.sh \
${PICARD_LIFTOVER_CONTAINER} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX} \
${BED_FILE_NAME} \
${GRCH38_REF} \
${HG19_TO_GRCH38_CHAIN} \
${SAMPLE_SHEET} \
${SUBMIT_STAMP}
}
# build a string of job names (comma delim) from the variant annotator scatter to store as variable to use as
# hold_jid for the cat variants gather (it's used in the next section after the for loop below)
GENERATE_CAT_REFINED_VARIANTS_HOLD_ID ()
{
CAT_REFINED_VARIANTS_HOLD_ID=${CAT_REFINED_VARIANTS_HOLD_ID}I${HACK}_${BED_FILE_NAME},
COMBINE_REFINED_LIFTOVER_VARIANTS_HOLD_ID=${COMBINE_REFINED_LIFTOVER_VARIANTS_HOLD_ID}I${HACK}K_${BED_FILE_NAME},
COMBINE_INITIAL_LIFTOVER_VARIANTS_HOLD_ID=${COMBINE_INITIAL_LIFTOVER_VARIANTS_HOLD_ID}I${HACK}L_${BED_FILE_NAME},
}
# for each chunk of the original bed file, do calculate_genotype_posteriors, then variant annotator
# then generate a string of all the variant annotator job names submitted
for BED_FILE in \
$(ls ${CORE_PATH}/${PROJECT_MS}/TEMP/BED_FILE_SPLIT/BF*);
do
BED_FILE_NAME=$(basename ${BED_FILE} .bed)
LIFTOVER_INITIAL_GRCH37_VCF_TO_HG19
echo sleep 0.1s
LIFTOVER_INITIAL_HG19_VCF_TO_HG38
echo sleep 0.1s
CALCULATE_GENOTYPE_POSTERIORS
echo sleep 0.1s
VARIANT_ANNOTATOR_REFINED
echo sleep 0.1s
LIFTOVER_GRCH37_TO_HG19_REFINED_ANNOTATED
echo sleep 0.1s
LIFTOVER_HG19_TO_GRCH38_REFINED_ANNOTATED
echo sleep 0.1s
GENERATE_CAT_REFINED_VARIANTS_HOLD_ID
done
#########################################################
#########################################################
##### GT Refined VCF Gather #############################
##### Multi-Sample VCF ANNOVAR ##########################
##### VARIANT SUMMARY STATS VCF BREAKOUTS ###############
#########################################################
#########################################################
# use cat variants to gather up all of the gt refined, reannotated vcf files above into one big file
CAT_REFINED_VARIANTS ()
{
echo \
qsub \
${QSUB_ARGS} \
-N J01_CAT_REFINED_VARIANTS_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/J01_CAT_REFINED_VARIANTS.log \
-hold_jid $CAT_REFINED_VARIANTS_HOLD_ID \
${COMMON_SCRIPT_DIR}/J01_CAT_REFINED_VARIANTS.sh \
${JAVA_1_8} \
${GATK_DIR} \
${REF_GENOME} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# use cat variants to gather up all of the gt refined, reannotated vcf files above into one big file
COMBINE_REFINED_LIFTOVER_GRCH38_VARIANTS ()
{
echo \
qsub \
${QSUB_ARGS} \
-N J02_COMBINE_REFINED_LIFTOVER_GRCH38_VARIANTS_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/J02_COMBINE_REFINED_LIFTOVER_GRCH38_VARIANTS.log \
-hold_jid ${COMBINE_REFINED_LIFTOVER_VARIANTS_HOLD_ID} \
${COMMON_GRCH37_SCRIPT_DIR}/J02_COMBINE_REFINED_LIFTOVER_GRCH38_VARIANTS.sh \
${JAVA_1_8} \
${GATK_DIR} \
${GRCH38_REF} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# use cat variants to gather up all of the gt refined, reannotated vcf files above into one big file
COMBINE_REFINED_LIFTOVER_GRCH38_REJECTED_VARIANTS ()
{
echo \
qsub \
${QSUB_ARGS} \
-N J03_CAT_REFINED_LIFTOVER_GRCH38_REJECTED_VARIANTS_${PROJECT_MS} \
-o ${CORE_PATH}/${PROJECT_MS}/LOGS/J03_COMBINE_REFINED_LIFTOVER_GRCH38_REJECTED_VARIANTS.log \
-hold_jid ${COMBINE_REFINED_LIFTOVER_VARIANTS_HOLD_ID} \
${COMMON_GRCH37_SCRIPT_DIR}/J03_COMBINE_REFINED_LIFTOVER_GRCH38_REJECTED_VARIANTS.sh \
${JAVA_1_8} \
${TABIX_DIR} \
${GATK_DIR} \
${GRCH38_REF} \
${CORE_PATH} \
${PROJECT_MS} \
${PREFIX}
}
# use cat variants to gather up all of the gt refined, reannotated vcf files above into one big file