Clinical research pipeline for exploring variants in PacBio HiFi whole genome (WGS) data (Hg38)

crg2-pacbio is a research pipeline aimed at discovering clinically relevant variants from PacBio HiFi whole genome sequence data in a family-based manner. crg2-pacbio uses Snakemake and Conda to manage jobs and software dependencies.

crg2-pacbio takes as input the following VCFs output by PacBio's WGS pipeline:

• DeepVariant joint-genotyped small variant VCF
• pbsv joint-genotyped structural variant VCF
• TRGT VCFs, one per family member
• aligned BAM files for each sample

How to run the pipeline

1. Make a folder in a directory with sufficient space. Copy over the template files crg2-pacbio/samples.tsv, crg2-pacbio/units.tsv, crg2-pacbio/config.yaml, crg2-pacbio/crg2-pacbio.sh, crg2-pacbio/slurm_profile/slurm-config.yaml. Note that 'slurm-config.yaml' is for submitting each rule as cluster jobs, so ignore this if not running on cluster.

mkdir NA12878
cp crg2-pacbio/samples.tsv crg2-pacbio/units.tsv crg2-pacbio/config.yaml crg2-pacbio/crg2-pacbio.sh crg2-pacbio/slurm_profile/slurm-config.yaml NA12878
cd NA12878

2. Set up pipeline run

• Reconfigure 'samples.tsv' and 'units.tsv' to reflect sample names and input files. Note that because several of the inputs are joint-genotyped, one row in the units.tsv file corresponds to one family, not one sample. 'units.tsv' must be configured with the path to the joint-genotyped deepvariant small_variant_vcf, the path to a directory containing per-sample genome-wide TRGT VCFs trgt_vcf_dir, and the joint-genotyped pbsv pbsv_vcf. The trgt_vcf_dir must ALSO contain the TRGT spanning BAMs to successfully run the denovo tandem repeat report. The 'samples.tsv' file should contain one row per family member, with the sample column corresponding to the family member ID and the BAM column corresponding to the path to the BAM file for that sample. units.tsv example:

family	platform	small_variant_vcf	trgt_vcf_dir	pbsv_vcf	trgt_pathogenic_vcf_dir
1042	PACBIO	/hpf/largeprojects/ccmbio/ccmmarvin_tcag_shared/PacBio/MEA26290/1042_TR0246.joint/1042_TR0246.joint.GRCh38.deepvariant.glnexus.phased.vcf.gz	trgt	/hpf/largeprojects/ccmbio/ccmmarvin_tcag_shared/PacBio/MEA26290/1042_TR0246.joint/1042_TR0246.joint.GRCh38.pbsv.phased.vcf.gz

samples.tsv example:

sample	BAM
01	/hpf/largeprojects/ccmbio/ccmmarvin_tcag_shared/PacBio/MEA26290/1042_TR0246/01.m84090_240206_172710_s2.hifi_reads.bc2010.KL.GRCh38.aligned.haplotagged.bam
02	/hpf/largeprojects/ccmbio/ccmmarvin_tcag_shared/PacBio/MEA26290/1042_TR0247/02.m84090_240206_192642_s3.hifi_reads.bc2011.KL.GRCh38.aligned.haplotagged.bam

• Add paths to the HPO term file and pedigree file to config.yaml.
• Do a dry run: add a -n flag to the Snakemake command in crg2-pacbio.sh. This will print out the rules that will be run, but not actually run them.
• If the dry run is successful, run the pipeline: sbatch crg2-pacbio.sh.
• If you just want to generate a single report, you can specify the report name in the Snakemake command in crg2-pacbio.sh. For example, to generate the repeat outlier report, add repeat_outliers/{family}.repeat.outliers.annotated.csv to the Snakemake command.

Example:

#!/bin/bash
#SBATCH --job-name=crg2-pacbio
#SBATCH --time=50:00:00
#SBATCH --ntasks-per-node=1
#SBATCH --mem=4G
#SBATCH --output=%x-%j.out

SF=~/crg2-pacbio/Snakefile
CP="/hpf/largeprojects/ccm_dccforge/dccdipg/Common/snakemake"
SLURM=~/crg2-pacbio/slurm_profile/
CONFIG="config.yaml"

source /hpf/largeprojects/ccm_dccforge/dccdipg/Common/anaconda3/etc/profile.d/conda.sh
conda activate snakemake

snakemake --use-conda -s ${SF} --cores 4 --conda-prefix ${CP} --configfile ${CONFIG} --profile ${SLURM} repeat_outliers/{family}.repeat.outliers.annotated.csv

Small variant annotation and report: small_variants/coding/{family}/{family}.wes.regular.{date}.csv

• annotate variants with VEP and vcfanno
• generate a gemini variant database
• generate a rare (less than 1% maximum gnomAD population AF) variant report with medium to high impact variants. Report generation scripts are derived from cre, but copied to this repo for convenience. Report details are described here; additional columns included are allele frequencies and counts from the CoLoRSDB cohort.

Small variant panel report: small_variants/panel/{family}/{family}.wgs.regular.{date}.csv, small_variants/panel-flank/{family}/{family}.wgs.regular.{date}.csv

• The annotation pipeline is the same as above, but only variants in a gene panel are considered. The panel report includes variants of any impact (i.e. it includes non-coding variants and intronic variants).
• To generate a gene panel from an HPO text file exported from PhenomeCentral or G4RD, add the HPO filepath to config["run"]["hpo"].
• The first time you run the pipeline, you will also need to generate Ensembl and RefSeq gene files as well as an HGNC gene mapping file.
• Download and unzip Ensembl gtf: wget -qO- https://ftp.ensembl.org/pub/release-112/gtf/homo_sapiens/Homo_sapiens.GRCh38.112.gtf.gz | gunzip -c > Homo_sapiens.GRCh38.112.gtf
• Download and unzip RefSeq gff: wget https://ftp.ncbi.nlm.nih.gov/refseq/H_sapiens/annotation/GRCh38_latest/refseq_identifiers/GRCh38_latest_genomic.gff.gz | gunzip -c > GRCh38_latest_genomic.gff
• Download RefSeq chromosome mapping file: wget https://ftp.ncbi.nlm.nih.gov/refseq/H_sapiens/annotation/GRCh38_latest/refseq_identifiers/GRCh38_latest_assembly_report.txt
• Run script to parse the above files: python scripts/clean_gtf.py --ensembl_gtf /path/to/Homo_sapiens.GRCh38.112.gtf --refseq_gff3 /path/to/GRCh38_latest_genomic.gff --refseq_assembly /path/to/GRCh38_latest_assembly_report.txt
• Add the paths to the output files, Homo_sapiens.GRCh38.112.gtf_subset.csv and GRCh38_latest_genomic.gff_subset.csv, to the config["gene"]["ensembl"] and config["gene"]["refseq"] fields.
• You will also need the HGNC alias file: download this from https://www.genenames.org/download/custom/ using the default fields. Add the path this file to config["gene"]["hgnc"].

Structural variant annotation and report: sv/{family}.pbsv.{date}.csv

• annotate variants using SnpEFF and AnnotSV
• filter out variants under 50bp
• annotate SVs with custom Python script
• a description of the report and fields can be found here

Repeat expansion outlier report: repeat_outliers/{family}.repeat.outliers.annotated.csv

• TRGT must have previously been run on each sample against the 937,122 repeats originally released by the Genome in a Bottle tandem repeat benchmarking project
• this module is derived from the find-outlier-expansions workflow developed by Egor Dolzhenko (PacBio), Adam English (Baylor College of Medicine), Tom Mokveld (PacBio), Giulia Del Gobbo (CHEO), and Madeline Couse (SickKids)
• construct a repeat database from 98 HPRC samples and the individuals from the family of interest
• identify repeats with outlying size in family members
• annnotate repeat outliers with custom Python script

De novo tandem repeat variant report: TRGT_denovo/{family}_{child}.TRGT.denovo.annotated.csv

• identify de novo tandem repeats in probands using TRGT-denovo v0.2.0
• note that the trgt_vcf_dir must contain the TRGT spanning BAMs to successfully run the denovo tandem repeat report
• filter annotate de novo repeats with custom Python script

Pathogenic repeat loci report: pathogenic_repeats/{family}.known.path.str.loci.csv

• genotype repeats per-sample using TRGTv1.0.0 against the pathogenic repeat loci BED file provided by TRGT (the GIAB 937,122 catalog only contains 50/56 loci). Note that TRGT requires BAMs; these must be added to the samples.tsv file
• merge sample VCFs into multi-sample family VCF
• annotate repeat loci with custom Python script