Welcome to NVIDIA Parabricks v4.7.1

pangenome_aware_deepvariant

Run a GPU-accelerated Pangenome-aware DeepVariant algorithm.

See the pangenome_aware_deepvariant Reference section for a detailed listing of all available options.

Pangenome-aware DeepVariant is an enhanced version of Google's DeepVariant that leverages pangenome reference graphs (GBZ files) to improve variant calling accuracy, particularly in complex and highly variable genomic regions. Traditional variant calling pipelines use a single linear reference genome, which can miss variants in regions that differ significantly from the reference. Pangenome-aware DeepVariant uses pangenome graphs that represent multiple haplotypes and structural variations, enabling more accurate variant detection in diverse populations. Like DeepVariant, Pangenome-aware Deepvariant generates pileup images and uses a CNN to infer genotypes. However, unlike DeepVariant, pileup images are generated for both the input reads and the pangenome haplotypes at potential variant positions. This allows directly using a pangenome for identifying true variants.

Linear genome references have been the standard for reference-based genomic analysis. However, linear references can introduce reference bias where the reference geneome is significantly different from the sample under study. Using a pangenome reference is one way to address this issue, since it includes diverse, non-redundant DNA sequences from multiple individuals. Pangenome-aware Deepvariant leverages the pangenome reference to outperform linear-reference-based DeepVariant by upto 25.5% across various short-read sequencing platforms and read mappers. Researchers from Google have also shown that Element reads with pangenome-aware DeepVariant can achieve 23.6% more accurate variant calling performance compared to existing methods.

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# This command assumes all the inputs are in the current working directory and all the outputs go to the same place. docker run --rm --gpus all --volume $(pwd):/workdir --volume $(pwd):/outputdir \ --workdir /workdir \ nvcr.io/nvidia/clara/clara-parabricks:4.7.1-1 \ pbrun pangenome_aware_deepvariant \ --ref /workdir/${REFERENCE_FILE} \ --pangenome /workdir/${GBZ_FILE} \ --in-bam /workdir/${INPUT_BAM} \ --out-variants /outputdir/${OUTPUT_VCF}

Use --sbx when calling variants from Roche SBX-D or SBX-Fast BAMs. Parabricks selects the SBX-trained pangenome-aware model (deepvariant_pangenome_aware_sbx.eng) for the current GPU architecture unless --pb-model-file overrides it, and applies make-examples and postprocess defaults aligned with the Google Roche SBX case study.

When --sbx is set, the following defaults apply:

  • Pileup image width of 301 base pairs.

  • alt_aligned_pileup=single_row pileup layout.

  • multiallelic_mode=product for multiallelic genotype resolution.

  • vsc_min_fraction_indels=0.08 and ws_min_base_quality=25.

  • --create-complex-alleles and --enable-strict-insertion-filter.

  • Insert-size pileup channel disabled by default (pass --channel-insert-size to enable it).

Roche SBX Quick Start

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# This command assumes all the inputs are in the current working directory and all the outputs go to the same place. docker run --rm --gpus all --volume $(pwd):/workdir --volume $(pwd):/outputdir \ --workdir /workdir \ nvcr.io/nvidia/clara/clara-parabricks:4.7.1-1 \ pbrun pangenome_aware_deepvariant \ --ref /workdir/${REFERENCE_FILE} \ --pangenome /workdir/${GBZ_FILE} \ --in-bam /workdir/HG002.roche_sbx.chr20.bam \ --out-variants /outputdir/HG002.chr20.output.vcf.gz \ --sbx \ -L chr20

Public case-study inputs (reference, GBZ, BAM, and GIAB truth sets) are available from the Google Roche SBX case study.

The command below shows the equivalent Google pangenome-aware DeepVariant command. Note that the Parabricks version provides the same accuracy with significant GPU acceleration.

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sudo docker run \ --volume <INPUT_DIR>:/input \ --volume <OUTPUT_DIR>:/output \ --shm-size 12gb \ google/pangenome_aware_deepvariant-1.9.0 \ /opt/deepvariant/bin/run_pangenome_aware_deepvariant \ --model_type WGS \ --ref /input/${REFERENCE_FILE} \ --reads /input/${INPUT_BAM} \ --pangenome /input/${GBZ_FILE} \ --output_vcf /output/${OUTPUT_VCF} \ --num_shards $(nproc) \ --make_examples_extra_args "ws_use_window_selector_model=true"

The command below shows the equivalent Google pangenome-aware DeepVariant Roche SBX command from the Roche SBX case study. Parabricks applies the same SBX defaults when --sbx is set.

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sudo docker run \ --volume <INPUT_DIR>:/input \ --volume <OUTPUT_DIR>:/output \ --volume <REFERENCE_DIR>:/reference \ --volume <MODEL_DIR>:/model \ --shm-size 12gb \ google/deepvariant:pangenome_aware_deepvariant-sbx \ /opt/deepvariant/bin/run_pangenome_aware_deepvariant \ --model_type WGS \ --ref /reference/${REFERENCE_FILE} \ --reads /input/HG002.roche_sbx.chr20.bam \ --pangenome /input/${GBZ_FILE} \ --output_vcf /output/HG002.chr20.output.vcf.gz \ --num_shards $(nproc) \ --regions chr20 \ --customized_model /model/model.ckpt \ --make_examples_extra_args="alt_aligned_pileup=single_row,create_complex_alleles=true,enable_strict_insertion_filter=true,keep_legacy_allele_counter_behavior=true,keep_only_window_spanning_haplotypes=true,keep_supplementary_alignments=true,min_mapping_quality=0,normalize_reads=true,pileup_image_height_pangenome=100,pileup_image_height_reads=100,pileup_image_width=301,sort_by_haplotypes=true,trim_reads_for_pileup=true,vsc_min_fraction_indels=0.08,ws_min_base_quality=25" \ --postprocess_variants_extra_args="multiallelic_mode=product"

While Parabricks Pangenome-aware DeepVariant does not lose any accuracy in functionality when compared with Google's Pangenome-aware DeepVariant, there are several reasons that can result in different output files:

  • CNN Inference

Google DeepVariant uses a CNN (convolutional neural network) to predict the possibilities of each variant candidate. The model is trained, and does inference through, Keras. In Parabricks DeepVariant we convert this Keras model to an engine file with TensorRT to perform accelerated deep learning inferencing on NVIDIA GPUs. Because of the optimizations from TensorRT, there is a small difference in the final possibility scores after inferencing (10^-5), which could cause a few different variants in the final VCF output. Based on current observations, the mismatches only happen to RefCalls with a quality score of zero.

  • Read Sorting Differences

The Google Pangenome-aware DeepVariant implementation uses sort instead of stable_sort for sorting reads based on position, fragment_name, and read_number. Unfortunately, when the keep-supplementary-alignments option is enabled, it is possible to have duplicate reads which are sorted non-deterministically by std::sort. The Parabricks implementation uses stable_sort to resolve this. To obtain identical results with Google's implementation, users are recommended to update the std::sort in BuildPileupForOneSample pileup_image_native.cc to std::stable_sort.

  • GBZ Reader Caching Mechanism

Google Pangenome-aware DeepVariant's GBZ reader includes a fast path to speed up queries to the pangenome graph. This fast path introduces non-determinism in the query operation to the pangenome where the result returned by the operation depends on the order of the previous queries to the pangenome. Since, Parabricks relies on multi-threading to achieve high performance, we disable the fast path in the Parabricks implementation. To obtain identical results using Google's implementation, users should comment out the call to updateCache in the GbzReader::Query() function in deepvariant/third_party/nucleus/io/gbz_reader.cc. Also, the check for whether the requested range is cached or not should be disabled (in the same function). Please note that disabling the cache can slow down Google Deepvariant significantly and is not recommended in general. We suggest this approach only for the purposes of comparing output accuracy.

Run pangenome_aware_deepvariant to convert BAM/CRAM to VCF.


Type

Name

Required?

Description

I/O --ref REF Yes Path to the reference file.
I/O --pangenome PANGENOME Yes Path to the pangenome gbz file.
I/O --in-bam IN_BAM Yes Path to the input BAM/CRAM file for variant calling.
I/O --interval-file INTERVAL_FILE No Path to a BED file (.bed) for selective access. This option can be used multiple times.
I/O --out-variants OUT_VARIANTS Yes Path of the vcf/vcf.gz/g.vcf/g.vcf.gz file after variant calling.
I/O --pb-model-file PB_MODEL_FILE No Path to a Parabricks TensorRT model (.eng) for pangenome_aware_deepvariant. Optional; if omitted, uses deepvariant_pangenome_aware.eng or deepvariant_pangenome_aware_sbx.eng when --sbx is set.
Tool --sbx No Roche SBX mode. Uses the shipped deepvariant_pangenome_aware_sbx.eng for the current GPU tier unless --pb-model-file overrides it.
Tool --disable-use-window-selector-model No Change the window selector model from Allele Count Linear to Variant Reads. This option will increase the accuracy and runtime.
Tool --norealign-reads No Do not locally realign reads before calling variants. Reads longer than 500 bp are never realigned.
Tool --vsc-min-fraction-indels VSC_MIN_FRACTION_INDELS No Indel alleles occurring at least this fraction of all counts in our AlleleCount will be advanced as candidates.
Tool --ws-min-base-quality WS_MIN_BASE_QUALITY No Minimum base quality to consider in calling a reference position for local assembly.
Tool --min-mapping-quality MIN_MAPPING_QUALITY No By default, reads with any mapping quality are kept. Setting this field to a positive integer i will only keep reads that have a MAPQ >= i. Note this only applies to aligned reads.
Tool --mode MODE No Value can be one of [shortread]. By default, it is shortread. (default: shortread)
Tool --pileup-image-width PILEUP_IMAGE_WIDTH No Pileup image width. Only change this if you know your model supports this width.
Tool --channel-insert-size No Enable the insert_size pileup channel. Without --sbx it is on by default. With --sbx it is off by default; pass this flag to enable it.
Tool --no-channel-insert-size No Disable the insert_size pileup channel. Without --sbx the channel is on by default; use this to turn it off. With --sbx the channel is already off unless --channel-insert-size is set. If both this flag and --channel-insert-size are set, the channel stays off. (default: False)
Tool --create-complex-alleles No Create complex alleles during calling.
Tool --enable-strict-insertion-filter No If True, add stricter filter for insertion in window selector. (experimental)
Tool --multiallelic-mode MULTIALLELIC_MODE No If True, use a specialized model for genotype resolution of multiallelic cases with two alts.
Tool --sample-name-pangenome SAMPLE_NAME_PANGENOME No Sample name to use for pangenome data. Default is 'pangenome'. (default: pangenome)
Tool --ref-name-pangenome REF_NAME_PANGENOME No Reference genome name for pangenome data. Default is 'GRCh38'. (default: GRCh38)
Tool -L INTERVAL, --interval INTERVAL No Interval within which to call the variants from the BAM/CRAM file. Overlapping intervals will be combined. Interval files should be passed using the --interval-file option. This option can be used multiple times (e.g. "-L chr1 -L chr2:10000 -L chr3:20000+ -L chr4:10000-20000").
Performance --num-cpu-threads-per-stream NUM_CPU_THREADS_PER_STREAM No Number of CPU threads to use per stream. (default: 6)
Performance --num-streams-per-gpu NUM_STREAMS_PER_GPU No Number of streams to use per GPU. Default is 'auto' which will try to use an optimal amount of streams based on the GPU. (default: auto)
Performance --run-partition No Divide the whole genome into multiple partitions and run multiple processes at the same time, each on one partition.
Performance --gpu-num-per-partition GPU_NUM_PER_PARTITION No Number of GPUs to use per partition.
Runtime --verbose No Enable verbose output.
Runtime --x3 No Show full command line arguments.
Runtime --logfile LOGFILE No Path to the log file. If not specified, messages will only be written to the standard error output.
Runtime --tmp-dir TMP_DIR No Full path to the directory where temporary files will be stored. (default: .)
Runtime --with-petagene-dir WITH_PETAGENE_DIR No Full path to the PetaGene installation directory. By default, this should have been installed at /opt/petagene. Use of this option also requires that the PetaLink library has been preloaded by setting the LD_PRELOAD environment variable. Optionally set the PETASUITE_REFPATH and PGCLOUD_CREDPATH environment variables that are used for data and credentials. Optionally set the PetaLinkMode environment variable that is used to further configure PetaLink, notably setting it to "+write" to enable outputting compressed BAM and .fastq files.
Runtime --keep-tmp No Do not delete the directory storing temporary files after completion.
Runtime --no-seccomp-override No Do not override seccomp options for docker.
Runtime --version No View compatible software versions.
Runtime --preserve-file-symlinks No Override default behavior to keep file symlinks intact and not resolve the symlink.
Runtime --num-gpus NUM_GPUS No Number of GPUs to use for a run. (default: 1)
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