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2 changes: 1 addition & 1 deletion scripts/vg_pedigree_scripts/setup_input_reads.sh
Original file line number Diff line number Diff line change
Expand Up @@ -86,7 +86,7 @@ if [ $RUN_SMALL_TEST == false ]; then
INDIVIDUAL_DATA_DIR="${INDIVIDUALS_DATA_DIR}/${SAMPLE_NAME}"
if [ $(find ${INDIVIDUAL_DATA_DIR}/ \( \( \( -wholename '*_R1*.fastq.gz' \) -not -wholename '*WES*' \) -not -wholename '*WTS*' \) | wc -l) -eq 1 ]; then
ln -s $(find ${INDIVIDUAL_DATA_DIR}/ \( \( \( -wholename '*_R1*.fastq.gz' \) -not -wholename '*WES*' \) -not -wholename '*WTS*' \) ) ${READ_DATA_DIR}/${SAMPLE_NAME}_read_pair_1.fq.gz
ln -s $(find ${INDIVIDUAL_DATA_DIR}/ \( \( \( -wholename '*_R1*.fastq.gz' \) -not -wholename '*WES*' \) -not -wholename '*WTS*' \) ) ${READ_DATA_DIR}/${SAMPLE_NAME}_read_pair_2.fq.gz
ln -s $(find ${INDIVIDUAL_DATA_DIR}/ \( \( \( -wholename '*_R2*.fastq.gz' \) -not -wholename '*WES*' \) -not -wholename '*WTS*' \) ) ${READ_DATA_DIR}/${SAMPLE_NAME}_read_pair_2.fq.gz
elif [ $(find ${INDIVIDUAL_DATA_DIR}/ \( \( \( -wholename '*_R1*.fastq.gz' \) -not -wholename '*WES*' \) -not -wholename '*WTS*' \) | wc -l) -gt 1 ]; then
PAIR_1_READS=()
PAIR_2_READS=()
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11 changes: 7 additions & 4 deletions scripts/vg_pedigree_scripts/setup_pedigree_script.sh
Original file line number Diff line number Diff line change
Expand Up @@ -236,6 +236,7 @@ ${RESTART_ARG} \\
--workDir ${COHORT_WORKFLOW_DIR}/tmp \\
--cleanWorkDir onSuccess \\
--whole_genome_config \\
--vg_docker 'quay.io/vgteam/vg:v1.31.0' \\
${COHORT_WORKFLOW_DIR}/${COHORT_NAME}_pedigree_jobstore \\
${COHORT_WORKFLOW_DIR}/${COHORT_NAME}_pedigree_outstore \\
${PROBAND_NAME} \\
Expand Down Expand Up @@ -275,8 +276,8 @@ ${SIB_READ_PAIR_LIST} \\
--snpeff_annotation \\
${DRAGEN_ARGS} \\
--run_analysis \\
--cadd_lines 100000 \\
--split_lines 100000 \\
--cadd_lines 30000 \\
--split_lines 30000 \\
--chrom_dir ${CHROM_ANNOT_DIR} \\
--edit_dir ${EDIT_ANNOT_DIR} \\
--cadd_data ${CADD_DATA_DIR} \\
Expand All @@ -293,6 +294,7 @@ ${RESTART_ARG} \\
--logFile ${COHORT_WORKFLOW_DIR}/${COHORT_NAME}_pedigree_workflow.log \\
--workDir ${COHORT_WORKFLOW_DIR}/tmp \\
--cleanWorkDir always \\
--vg_docker 'quay.io/vgteam/vg:v1.31.0' \\
${COHORT_WORKFLOW_DIR}/${COHORT_NAME}_pedigree_jobstore \\
${COHORT_WORKFLOW_DIR}/${COHORT_NAME}_pedigree_outstore \\
${PROBAND_NAME} \\
Expand Down Expand Up @@ -341,6 +343,7 @@ ${RESTART_ARG} \\
--workDir ${COHORT_WORKFLOW_DIR}/tmp \\
--cleanWorkDir onSuccess \\
--whole_genome_config \\
--vg_docker 'quay.io/vgteam/vg:v1.31.0' \\
${COHORT_WORKFLOW_DIR}/${COHORT_NAME}_pedigree_jobstore \\
${COHORT_WORKFLOW_DIR}/${COHORT_NAME}_pedigree_outstore \\
${PROBAND_NAME} \\
Expand Down Expand Up @@ -379,8 +382,8 @@ ${SIB_READ_PAIR_LIST} \\
--snpeff_annotation \\
${DRAGEN_ARGS} \\
--run_analysis \\
--cadd_lines 100000 \\
--split_lines 100000 \\
--cadd_lines 30000 \\
--split_lines 30000 \\
--chrom_dir ${CHROM_ANNOT_DIR} \\
--edit_dir ${EDIT_ANNOT_DIR} \\
--cadd_data ${CADD_DATA_DIR} \\
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6 changes: 3 additions & 3 deletions src/toil_vg/vg_config.py
Original file line number Diff line number Diff line change
Expand Up @@ -254,7 +254,7 @@
glnexus-docker: 'quay.io/mlin/glnexus:v1.2.7'

# Docker image to use for abra2
abra2-docker: 'dceoy/abra2:latest'
abra2-docker: 'quay.io/biocontainers/abra2:2.24--h7d875b9_0'

# Docker image to use for deeptrio
deeptrio-docker: 'google/deepvariant:deeptrio-1.1.0'
Expand Down Expand Up @@ -394,7 +394,7 @@

# Resources allotted for xg indexing by chromosome (used for GBWT).
gbwt-index-cores: 4
gbwt-index-mem: '50G'
gbwt-index-mem: '10G'
gbwt-index-disk: '100G'
gbwt-index-preemptable: True

Expand Down Expand Up @@ -584,7 +584,7 @@
glnexus-docker: 'quay.io/mlin/glnexus:v1.2.7'

# Docker image to use for abra2
abra2-docker: 'dceoy/abra2:latest'
abra2-docker: 'quay.io/biocontainers/abra2:2.24--h7d875b9_0'

# Docker image to use for deeptrio
deeptrio-docker: 'google/deepvariant:deeptrio-1.1.0'
Expand Down
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