Evidence map›Paper›PMID 42330012›Full record

ArticlePLoS computational biology2026

GrassSV - hybrid method to detect structural variants in high throughput DNA-seq data.

Dominik Witczak, Krzysztof Sychla, Julia Wysocka, Artur Laskowski, Wojciech Frohmberg, Marta Glowacka, Alicja Dzik, Piotr Lukasiak, Jacek Blazewicz, Aleksandra Swiercz

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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Dominik WitczakInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Krzysztof SychlaInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Julia WysockaInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Artur LaskowskiInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Wojciech FrohmbergInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Marta GlowackaInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Alicja DzikInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Piotr LukasiakInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Jacek BlazewiczInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Aleksandra SwierczInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.ORCID https://orcid.org/0000-0002-5574-8222

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic diversity is crucial for populations to adapt and survive in dynamic environments. This diversity arises from genetic mutations, which manifest in the genome as structural variants (SVs). Several types of SVs exist, but not all are equally easy to detect. Current SV detection tools tend to specialize in certain SV types or require the use of multiple tools to obtain a comprehensive variant profile, which increases computational cost and complexity. While some methods excel at identifying breakpoints, they often struggle with accurately classifying variant types, and their precision depends strongly on data quality and sequencing technology. At present, the majority of available genomic data originates from high-quality short reads, which remain the most affordable sequencing technology. In this manuscript, we introduce GrassSV, a novel and computationally efficient method that employs a hybrid pattern-matching approach to detect all major classes of structural variants using short-read sequencing data. GrassSV integrates depth-of-coverage analysis with contig-based pattern recognition to ensure both sensitivity and precision while minimizing false positives and runtime. Its robustness was demonstrated on the human Genome in a Bottle dataset, as well as on synthetic data derived from the yeast genome, where it achieved high accuracy across all SV types at a lower computational cost compared to existing methods. This makes GrassSV a practical alternative to multi-tool pipelines typically required for comprehensive SV detection. GrassSV is available at https://github.com/Domomod/GrassSV under GPL-3.0 license and the benchmark at: https://github.com/Domomod/GrassBenchmark.

Indexed as

Genomic Structural VariationHigh-Throughput Nucleotide SequencingSequence Analysis, DNAAlgorithmsComputational BiologyGenetic VariationGenome, HumanGenomicsHumansSoftware

Identifiers

PMID42330012
PMCPMC13309023

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.