VUSVista: Enhancing the Curation of Variants of Uncertain Significance
Abstract
BackgroundThe increased demand for genomic sequencing has consequently led to a rise in the number of Variants of Uncertain Significance (VUS), which are classified as such due to insufficient evidence to determine their pathogenicity. VUS lead to incomplete diagnosis for patients, potentially causing anxiety due to the uncertainty associated with VUS and resulting in suboptimal management. ResultsWe developed a software, VUSVista, for organised and semi-automated VUS curation. It offers American College of Medical Genetics and Genomics (ACMG) criteria management, external database references, standardised Human Phenotype Ontology (HPO) terms for sample phenotypes, links between variants and pseudonymised samples as well as audit trails. VUSVista automatically checks for updates to ClinVars germline classification entries of recorded VUS and searches for newly released publications referencing its VUS using Lit-Var 2.0. Users are notified whenever a ClinVar entry is updated or a relevant publication is found, helping them stay informed about new scientific discoveries. Assessing the significance of this new evidence may lead to VUS reclassification through VUSVista. One-to-one sessions and a focus group were conducted with medical laboratory scientists and a senior pharmacist to validate the system. ConclusionsOverall, VUSVista facilitates VUS curation and reclassification, increasing the likelihood that patients receive a comprehensive diagnosis and the most appropriate treatment. Its implementation is publicly available on GitHub (https://github.com/estherspiteri/VUSVista).
02 /Specification & Classification
Click any tag to browse matching papersReproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Distinct rates of VUS reclassification are observed when subclassifying VUS by evidence level
Gwendolyn Bennett, Izabela Karbassi, … Heidi L. Rehm·Genetics in MedicinePeer-reviewed·Feb 28, 2025
- ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines
Christine G. Preston, Matt W. Wright, … Helio A. Costa·Genome MedicinePeer-reviewed·Jan 17, 2022
- Language models reveal evidence gaps in variants of uncertain significance
Weijiang Li, Vineel Bhat, … Christopher A. Cassa·medRxiv·Mar 2, 2026
- A scalable approach to resolving variants of uncertain significance
Malvika Tejura, Y P Chen, … Lea M. Starita·bioRxiv·Feb 23, 2026
- From Uncertain to Actionable: Significant Reduction in Variants of Uncertain Significance in Hereditary Germline Testing via Multi-Institutional Real-World Evidence
Kelly M. Schiabor Barrett, Matthew J. Ferber, … Elizabeth T. Cirulli·medRxiv·Aug 12, 2025
- The ten year evolution of Sherloc, a points-based framework for genetic variant classification
Yuya Kobayashi, Marjorie Jody Westbrook, … Robert D. Daber·medRxiv·Nov 24, 2025