Journal Article

Benchmarking UMI-aware and standard variant callers for low frequency ctDNA variant detection

Brierley, Liam, Fowler, Anna, Jorgensen, Andrea, Maruzani, Rugare

2024

Overview

Background Circulating tumour DNA (ctDNA) is a subset of cell free DNA (cfDNA) released by tumour cells into the bloodstream. Circulating tumour DNA has shown great potential as a biomarker to inform treatment in cancer patients. Collecting ctDNA is minimally invasive and reflects the entire genetic makeup of a patient’s cancer. ctDNA variants in NGS data can be difficult to distinguish from sequencing and PCR artefacts due to low abundance, particularly in the early stages of cancer. Unique Molecular Identifiers (UMIs) are short sequences ligated to the sequencing library before amplification. These sequences are useful for filtering out low frequency artefacts. The utility of ctDNA as a cancer biomarker depends on accurate detection of cancer variants. Results In this study, we benchmarked six variant calling tools, including two UMI-aware callers for their ability to call ctDNA variants. The standard variant callers tested included Mutect2, bcftools, LoFreq and FreeBayes. The UMI-aware variant callers benchmarked were UMI-VarCal and UMIErrorCorrect. We used both datasets with known variants spiked in at low frequencies, and datasets containing ctDNA, and generated synthetic UMI sequences for these datasets. Variant callers displayed different preferences for sensitivity and specificity. Mutect2 showed high sensitivity, while returning more privately called variants than any other caller in data without synthetic UMIs – an indicator of false positive variant discovery. In data encoded with synthetic UMIs, UMI-VarCal detected fewer putative false positive variants than all other callers in synthetic datasets. Mutect2 showed a balance between high sensitivity and specificity in data encoded with synthetic UMIs. Conclusions Our results indicate UMI-aware variant callers have potential to improve sensitivity and specificity in calling low frequency ctDNA variants over standard variant calling tools. There is a growing need for further development of UMI-aware variant calling tools if effective early detection methods for cancer using ctDNA samples are to be realised.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Analysis / Animal Genetics and Genomics / Artifact identification / Benchmarking / Benchmarks / Biological markers / Biomarkers / Biomarkers, Tumor - blood / Biomarkers, Tumor - genetics / Biomedical and Life Sciences / Biopsy / Breast cancer / Cancer / Circulating Tumor DNA - blood / Circulating Tumor DNA - genetics / ctDNA / Datasets / Deoxyribonucleic acid / Diagnosis / DNA / DNA methylation / DNA sequencing / Gene sequencing / Genetic Variation / High-Throughput Nucleotide Sequencing - methods / Humans / Life Sciences / Low frequencies / Metastasis / Methods / Microarrays / Microbial Genetics and Genomics / Mortality / Mutation / Neoplasms - blood / Neoplasms - genetics / Next generation sequencing / Nucleotide sequence / Plant Genetics and Genomics / Proteomics / Sensitivity / Sensitivity and Specificity / Sequence Analysis, DNA - methods / Software / Synthetic data / Tumors / Variant calling