Variants of uncertain significance (VUS) are the most frequent outcome in germline genetic testing, with almost 30% of patients receiving only VUS results. This delays clinical decisions and forces manual review, complicating the interpretation of...

Community VarSome.com Events

Reclassification of VUS with VarSome

By Lyndsey Fletcher on June 19, 2026

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VarSome Clinical now includes an Overlap with Known SVs column within the Structural Variant Table. This new feature provides an immediate view of how a copy number variant overlaps with previously reported SVs, supporting faster and more consistent...

VarSome Clinical News

Overlap with Known Structural Variants in VarSome Clinical

By Jason Armstrong on March 16, 2026

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Our fusion annotation solution is built for routine somatic oncology workflows. Upload TSV or CSV files from widely used fusion callers across amplicon and hybrid capture assays, and review annotated fusion events in a structured format. RNA fusion...

VarSome Clinical News Oncology

RNA Fusion Annotation in VarSome Clinical

By Jason Armstrong on March 16, 2026

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Updated 16th March 2026 In clinical genomics, you are often confronted with fragmented, siloed data sources in different formats and the constant challenge of bringing together disparate sets of evidence. To provide you with a comprehensive and...

Technology VarSome Clinical VarSome Team Oncology Germline KnowledgeHub

MolecularDB: A Unified Source for Genomic Data Analysis

By Jason Armstrong on November 19, 2025

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Technology VarSome Clinical VarSome Team Germline KnowledgeHub

VarSome Picks: Algorithmic Prioritization That Thinks Like a Clinician

By Jason Armstrong on November 13, 2025

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Lausanne, 17 October, 2025 — Sciencewerke, a leading provider of biomedical and life science solutions, is proud to announce its appointment as the official distributor for VarSome, the comprehensive platform for genomic variant interpretation and...

Press Releases VarSome Clinical News

Sciencewerke Appointed Official Distributor for VarSome in Australia, Malaysia, Singapore, and Thailand

By Xanthippi Papakonstanti on October 17, 2025

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Interpreting genomic variants is one of the most time-consuming and complex tasks in clinical genomics. Each variant must be assessed for its clinical significance using established guidelines (where available), curated databases, and the latest...

VarSome Clinical Oncology Germline

Automated Germline and Somatic Classification

By Jason Armstrong on September 22, 2025

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VarSome Clinical is a CE IVDR-certified, HIPAA-compliant platform for interpreting NGS data. It supports analysis of genomes, exomes, and gene panels from individual samples, trios, families, or cohorts.

VarSome Clinical Oncology Germline

Germline and Somatic Pipelines

By Jason Armstrong on September 22, 2025

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Updated 16th March 2026 VarSome Clinical offers two types of filtering: algorithmic filters, which run during analysis to prioritize variants, and dynamic filters, which give you flexible control over how results are viewed and explored.Together,...

VarSome Clinical Oncology Germline

Algorithmic and Dynamic Filters

By Jason Armstrong on September 22, 2025

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VarSome Clinical is designed to process NGS data, from gene panels to whole genomes, and supports FASTQ or VCF files. To effectively use the platform, it's important to understand the data upload methods and the specific requirements for different...

VarSome Clinical

File Uploads - VarSome Clinical

By Jason Armstrong on September 22, 2025

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Each year, International Programmers’ Day is marked on the 256th day of the calendar. This number is chosen because 256 is both the total number of values an eight-bit byte can represent and the largest power of 2 below 365. Depending on the year,...

Community Technology Awareness Days

International Programmers' Day 2025

By Jason Armstrong on September 12, 2025

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