ArticleBriefings in bioinformatics2025
SVHunter: long-read-based structural variation detection through the transformer model.
Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.
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.
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Who cites it
7 citing papers in PubMed.
- Comprehensive evaluation of structural variation detection for germline and somatic analysis with long-read sequencing data.Briefings in bioinformatics · 2026Article
- nf-core/pacsomatic: a scalable somatic analytic pipeline using PacBio HiFi data.Bioinformatics (Oxford, England) · 2026Article
- Dual-SVF: a robust knowledge-guided multimodal method for structural variant filtering in long-read sequencing.Briefings in bioinformatics · 2026Article
- MRDsteer: quality-aware AI-driven closed-loop optimization enhances ctDNA-based minimal residual disease detection.Briefings in bioinformatics · 2026Article
- Article
- MRDadaptis: self-adaptive parameter configuration enhances minimal residual disease detection in heterogeneous ctDNA samples.Briefings in bioinformatics · 2025Article
- Long-Read Sequencing and Structural Variant Detection: Unlocking the Hidden Genome in Rare Genetic Disorders.Diagnostics (Basel, Switzerland) · 2025Review
Corrections and comments
- Erratum issued
Authors and funding
7 authors.
Funding
Abstract
Structural variations (SVs) are genomic rearrangements larger than 50 bp, that are widely present in the human genome and are associated with various complex diseases. Existing long-read-based SV detection tools often rely on fixed rules or heuristic algorithms, which can oversimplify the complexity of SV signatures. Therefore, these methods usually lack flexibility and cannot fully capture SV signals, leading to reduced accuracy and robustness. To address these issues, we propose SVHunter, a transformer-based method for long-read SV detection. SVHunter combines convolutional neural networks and transformers to capture both local and global SV signatures, enabling accurate identification of SVs. Additionally, SVHunter employs the mean shift clustering algorithm, which dynamically adjusts bandwidth parameters to accommodate different types of SVs without requiring a preset number of clusters, thus allowing precise breakpoint clustering. Validation across multiple sequencing platforms and datasets demonstrates that SVHunter excels at detecting various types of SVs, with a notable reduction in the false discovery rate. This highlights considerable strong potential for both research and clinical applications.
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Registered trials
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.