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 integrated solution, we...
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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
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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
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, they help reduce noise...
VarSome Clinical Oncology Germline
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...
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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,...
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Did you know you can search the entire VarSome knowledge base using plain text? Whether you’re investigating a specific gene, variant, condition, or concept, VarSome’s full text search helps you find relevant content quickly, without needing...
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Tumor mutational burden (TMB) and Microsatellite Instability (MSI) are now established biomarkers guiding immunotherapy decisions across a growing list of solid tumors. This article outlines how TMB and MSI are defined and assessed in VarSome...
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VarSome Clinical now lets you build report templates that match your laboratory's requirements.
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Mapping cyber threats in sequencing, analysis, and reporting.
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Wong M, Liew B, Hum M, Lee NY, Lee ASG. Benchmarking of variant calling software for whole-exome sequencing using gold standard datasets. Sci Rep. 2025;15(1):13697. doi:10.1038/s41598-025-97047-7
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