HiFi somatic WDL

A tumor-normal variant-calling workflow for HiFi data

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Table of contents

• Table of contents
• Installation and Dependencies
• Usage
• Important outputs from workflow
• Demo datasets and accuracy of the workflow
• References
• Tools versions
• Change logs
• DISCLAIMER

Installation and Dependencies

The workflow is written in WDL version 1.0 (Workflow Description Language). It depends on miniwdl and singularity (version 3 and later). miniwdl can be installed using Bioconda. The workflow can also be run using Cromwell. (See here for instructions, tested on version 86).

Usage

A step-by-step tutorial demonstrating usage and an FAQ can be found here.

Important outputs from workflow

The workflow will generate the following (non-exhaustive list) results in the $OUTDIR/_LAST/out folder. Please refer to output for a more detailed description of the outputs. An example of final HTML report from COLO829 dataset can be found here (Right click to save the file and double click to open it in a web browser).

Folder	Types of results
AnnotatedSeverusSV	Severus structural variants annotated with AnnotSV (TSV, see AnnotSV README)
Annotated*SV_intogen	Structural variants annotated with AnnotSV (TSV) overlapping with the Compendium of Cancer Genes (IntOGen May 23)
small_variant_vcf_annotated	DeepSomatic or ClairS SNV/INDEL annotated with VEP (VCF, single entry per variant with --pick, see VEP documentation)
small_variant_tsv_annotated	VEP annotation for SNV/INDEL in TSV format
small_variant_tsv_CCG	SNV/INDEL that are in the Compendium of Cancer Genes (IntOGen May 23)
mutsig_SNV_profile	Mutational profile plot (MutationalPattern)
mutsig_SNV	Mutational signature in TSV format (MutationalPattern)
normal_germline_small_variant_vcf_annotated	ClairS/Clair3 germline SNV/INDEL (In normal sample) annotated with VEP (Optional, see input JSON parameters)
DMR_annotated	Differentially methylated region annotated with genes/introns/promoters etc (TSV)
DMR_results	Raw differentially methylated region from DSS (Unannotated, TSV)
DMR_annotated_CCG	Annotated DMR (>50 CpG sites) overlapping with the Compendium of Cancer Genes (IntOGen May 23)
mosdepth_normal_summary	Depth of coverage of normal (TXT)
mosdepth_tumor_summary	Depth of coverage of tumor (TXT)
normal_bams_phased	Phased normal BAM file (Hiphase)
tumor_bams_hiphase	Phased tumor BAM file (Hiphase)
tumor_bams_longphase	Phased tumor BAM file (Optionally, use Longphase for phasing. See input JSON parameters)
overall_(tumor|normal)_alignment_stats	Alignment overall statistics (Mapped %)
per_alignment_(tumor|normal)_stats	Statistics (accuracy/n_mismatches/length) for each alignment
aligned_RL_summary_(tumor|normal)	Aligned read length N50, mean and median
normal_germline_small_variant_vcf	Germline variants in normal (VCF)
tumor_germline_small_variant_vcf	Germline variants in tumor (VCF)
pileup_(normal/tumor)_bed	Summarized 5mC probability  in normal and tumor (BED, see pb-CpG-tools for format description)
cnvkit_cns_with_major_minor_CN	Copy number segments adjusted with purity and ploidy estimate, see cnvkit_output for raw CNVKit result (BED)
Severus_filtered_vcf	Severus structural variants (filtered with control VCF and has simple annotation based on svpack)
small_variant_vcf	DeepSomatic or ClairS SNV/INDEL (Unannotated VCF)
Purple_outputs	Purity and ploidy estimate + allele-specific copy number calls from HMFtools suite
chord_hrd_prediction	Homologous recombination deficiency (HRD) prediction using CHORD
report	HTML report summarizing the results. This can be open in any modern web browser. The report is only generated if all steps in the pipeline is carried out (e.g. small variants calling, SV annotation)

Demo datasets and accuracy of the workflow

There are two cancer cell lines sequenced on Revio systems, provided by PacBio:

1. COLO829 (60X tumor, 60X normal): https://downloads.pacbcloud.com/public/revio/2023Q2/COLO829
2. HCC1395 (60X tumor, 40X normal): https://downloads.pacbcloud.com/public/revio/2023Q2/HCC1395/

A benchmark of both cell lines can be found here.

References

References of tools used

Following are the references for the tools used in the workflow, which should be cited if you use the workflow. The list may not be exhaustive; we welcome suggestions for additional references.

1. Zheng, Z. et al. ClairS: a deep-learning method for long-read somatic small variant calling. 2023.08.17.553778 Preprint at https://doi.org/10.1101/2023.08.17.553778 (2023).
2. English, A. C., Menon, V. K., Gibbs, R. A., Metcalf, G. A. & Sedlazeck, F. J. Truvari: refined structural variant comparison preserves allelic diversity. Genome Biology 23, 271 (2022).
3. Wang, T. et al. The Human Pangenome Project: a global resource to map genomic diversity. Nature 604, 437–446 (2022).
4. Danecek, P. et al. Twelve years of SAMtools and BCFtools. GigaScience 10, giab008 (2021).
5. Li, H. Minimap2: pairwise alignment for nucleotide sequences. Bioinformatics 34, 3094–3100 (2018).
6. Sedlazeck, F. J. et al. Accurate detection of complex structural variations using single molecule sequencing. Nat Methods 15, 461–468 (2018).
7. Pedersen, B. S. & Quinlan, A. R. Mosdepth: quick coverage calculation for genomes and exomes. Bioinformatics 34, 867–868 (2018).
8. McLaren, W. et al. The Ensembl Variant Effect Predictor. Genome Biology 17, 122 (2016).
9. Park, Y. & Wu, H. Differential methylation analysis for BS-seq data under general experimental design. Bioinformatics 32, 1446–1453 (2016).
10. Talevich, E., Shain, A. H., Botton, T. & Bastian, B. C. CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing. PLoS Comput Biol 12, e1004873 (2016).
11. Martínez-Jiménez, F. et al. A compendium of mutational cancer driver genes. Nat Rev Cancer 20, 555–572 (2020). https://www.intogen.org
12. Manders, F. et al. MutationalPatterns: the one stop shop for the analysis of mutational processes. BMC Genomics 23, 134 (2022).
13. Lin, J.-H., Chen, L.-C., Yu, S.-C. & Huang, Y.-T. LongPhase: an ultra-fast chromosome-scale phasing algorithm for small and large variants. Bioinformatics 38, 1816–1822 (2022).
14. HMFtools suite (Amber, Cobalt and Purple): https://github.com/hartwigmedical/hmftools/tree/master

Tools versions

Tools used in the workflow

Tool	Version	Purpose
pbmm2	1.12.0	Alignment of HiFi reads
pbtk	3.1.0	Merging HiFi reads
samtools	1.17	Various tasks manipulating BAM files
VEP	110.1	Annotation of small variants
AnnotSV	3.3.6	Annotation of structural variants
DSS	2.48.0	Differential methylation
annotatr	1.26.0	Annotation of differentially methylated region (DMR)
ClairS	0.1.6	Somatic SNV and INDEL caller
bcftools	1.17	Manipulation of VCF
CNVKit	0.9.10	Copy number segmentation
Truvari	4.0.0	Filtering of control structural variants (Deprecated, using svpack instead)
bedtools	2.31.0	Splitting genome intervals for parallelization
mosdepth	0.3.4	Calculating depth of coverage
pb-CpG-tools	2.3.1	Summarizing 5mC probability
HiPhase	1.1.0	Diploid phasing using germline variants
slivar	0.3.0	Selecting/filtering variants from VCF
Severus	v0.1.1	Structural variants
seqkit	2.5.1	Aligned BAM statistics
csvtk	0.27.2	Aligned BAM statistics summary and other CSV/TSV operation
IntOGen	May 31 2023	Compendium of Cancer Genes for annotation
MutationalPattern	3.10.0	Mutational signatures based on SNV
Longphase	v1.5.2	Optional phasing tool
Amber	v4.0	BAF segmentation (HMFtools suite)
Cobalt	v1.16.0	Log ratio segmentation (HMFtools suite)
Purple	v4.0	Purity and ploidy estimate, somatic CNV (HMFtools suite)
DeepSomatic	v1.6.0	Somatic SNV/INDELs caller
CHORD	v2.0.0	HRD prediction

Change logs

Click to expand changelogs:

• v0.6.2:

  • Added experimental CHORD HRD (Homologous Recombination Deficiency) prediction. See here for details.
  • Renamed some variables (legacy Sniffles parameters).
  • Swap CNVkit visualization to Purple in report.
  • Made changes in WDL for compatibility with Cromwell.
  • Allow specifying min/max purity/ploidy for Purple (In task WDL)

• v0.6.1:

  • Updated documentation and benchmark.
  • Small bugfix in tabix indexing of VCFs.
  • Added HTML report for summary metrics.
  • Fixed a bug where germline VCFs are not output when using DeepSomatic.
  • Fixed a bug introduced in svpack filtering where entries with SVLEN=0. are filtered out (They should not be).

• v0.6:

  • Added DeepSomatic 1.6.0 (Experimental and disabled by default. Enable with hifisomatic.use_deepsomatic in input JSON). Note that DeepSomatic is computationally expensive compared to ClairS so we recommend disabling it if computational resources are limited. See benchmark here for comparison between ClairS and DeepSomatic.
  • Use svpack to filter for control SVs (previously using truvari) and provide simple annotation in filtered VCF.
  • Switch to using samtools to strip kinetics.

• v0.5:

  • Updated Cobalt to 4.0. It now counts read depth correctly. See here for details.
  • Containers are now on pacbio quay.io.
  • SV calling now only uses Severus.
  • Individual tasks now output the version number in stdout.

• v0.4:

  • Added purity, ploidy and somatic CNV with Amber, Cobalt and Purple
    • Note that Cobalt doesn't count the read depth from long-reads correctly so it'll affect the segmentation accuracy. However, purity and ploidy estimation appears to be robust.
  • CNVKit segmentation results recalled with purity and ploidy estimate from Purple.
  • Severus release now updated with Bioconda container.
  • Fixed an issue when call_smallvariants is set to false (Issue #1).

• v0.3:

  • Added IntOGen filtering of SV/SNV/INDEL/DMR.
  • Added mutational signature analysis.
  • Added germline small variants annotation with VEP (optional).
  • Added Longphase as an optional phasing tool.
  • Better documentation of output in output.

• v0.2:

  • Downgraded to WDL 1.0 for better compatibility.
  • Added run time attribute to tasks for future support on cloud (not tested yet).

• v0.1: Initial release.

DISCLAIMER

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