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Truvari: refined structural variant comparison preserves allelic diversity

Adam C. English, Vipin K. Menon, Richard A. Gibbs, Ginger Metcalf, Fritz J. Sedlazeck

2022Genome biology231 citationsDOIOpen Access PDF

Abstract

The fundamental challenge of multi-sample structural variant (SV) analysis such as merging and benchmarking is identifying when two SVs are the same. Common approaches for comparing SVs were developed alongside technologies which produce ill-defined boundaries. As SV detection becomes more exact, algorithms to preserve this refined signal are needed. Here, we present Truvari-an SV comparison, annotation, and analysis toolkit-and demonstrate the effect of SV comparison choices by building population-level VCFs from 36 haplotype-resolved long-read assemblies. We observe over-merging from other SV merging approaches which cause up to a 2.2× inflation of allele frequency, relative to Truvari.

Topics & Concepts

BiologyHuman geneticsEvolutionary biologyAlleleDiversity (politics)GeneticsComputational biologyComputational genomicsGenetic diversityGenomicsGenomeGenePopulationAnthropologyDemographySociologyChromosomal and Genetic VariationsGenomics and Rare DiseasesGenomics and Chromatin Dynamics
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