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POSTER

Using a Knowledgebase of Clinical Assertions to Identify Potential Therapy Targets for Investigation in Underserved Cancers

Despite the recognized oncogenicity of certain gene alterations, many still lack established therapeutic options...
Despite the recognized oncogenicity of certain gene alterations, many still lack established therapeutic options...
WHITEPAPER

Elevate Your LDTs

A Blueprint for Success in Precision Genomics for Oncology. In the rapidly advancing field of precision oncology, a critical bottleneck in patient care is selecting the most relevant molecular test and using it to identify and accurately interpret the genetic alterations identifi...
A Blueprint for Success in Precision Genomics for Oncology. In the rapidly advancing field of precision oncology, a critical bottleneck in patient care is selecting the most relevant molecular test and using it to identify and acc...
WHITEPAPER

Inherited Cancer Testing

A laboratory guide to hereditary cancer testing.
A laboratory guide to hereditary cancer testing.
POSTER

Perspectives on FDA’s Final Rule on Laboratory Developed Tests:
Understanding the Impacts of IVD Requirements on Test Manufacturers who are Laboratories

The FDA’s new ruling on Laboratory...
The FDA’s new ruling on Laboratory...
POSTER

Consistency of Analytical Performance Characteristics and Other Observed Trends from the Validation of comprehensive Genomic Profiling LDTs by Diverse Laboratories 

Validation of comprehensive..
Validation of comprehensive..
TECHNOTE

Velsera Clinical Genomics Knowledgebase:

Rapidly, accurately identify clinically significant variants and produce an actionable report

This technical note describes the Velsera Knowledgebase in the context of somatic cancer biomarker reporting.
This technical note describes the Velsera Knowledgebase in the context of somatic cancer biomarker reporting.
POSTER

Orthogonal Approaches to Validate the Velsera Knowledgebase, a Precision Oncology Knowledgebase that Supports Automated Reporting of Clinically Relevant Somatic Cancer Variants.

Deciphering cancer genome alterations and treatment options is complex due to the diverse technologies and therapies available...
Deciphering cancer genome alterations and treatment options is complex due to the diverse technologies and therapies available...
POSTER

CGW Plus: A New Standard In Clinical Genomics Reporting

Discover how Velsera’s reimagined Clinical Genomics Workspace (CGW) Plus is transforming the way clinical laboratories handle genomic data. Based on over a decade of customer insights and...
Discover how Velsera’s reimagined Clinical Genomics Workspace (CGW) Plus is transforming the way clinical laboratories handle genomic data. Based on over a decade of customer insights and...
Blog

Insights from Velsera.

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Velsera Blog

Community is the Key to Progress with Precision Medicine

Our User Conference, Better. Faster. Simpler. Accelerate Your Capabilities with Velsera,...
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Velsera Blog

Make Training Great Again: Maximize Your Innovation Investment with a Tailored Training Plan

We all know how important training is in the workplace; our new starters can’t get to...
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Velsera Blog

A Winning Methodology: Key Criteria for Success in Launching an NGS assay

Consider this: your company has decided to bring on a new next-generation sequencing...
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EXPLORE OUR PRODUCTS

Document library.

BROCHURE

The Seven Bridges Platform

Accelerating your drug discovery process with Velsera's enterprise-grade bioinformatics ecosystem.

BROCHURE

GRAF

A better approach to NGS data analysis: building a pan-genome graph containing population genetics. 

BROCHURE

ARIA

Robust analysis on integrated genomic and phenotypic data. 

BROCHURE

Clinical Genomics Workspace

All-in-one analysis and reporting tool for clinical NGS data, enhancing the quality and efficiency of patient care delivery. 

BROCHURE

FastFinder

A secure and reliable platform for molecular diagnostics. 

on-demand

Video library.

CGW Plus webinar Social images
September 10, 2024
Tackling Complexity in Oncology Biomarker Interpretation with CGW Plus.

A discussion of challenges and innovative solutions in clinical genomics workflows. Discover how laboratories leverage variant databases and medical genomics knowledge to automate and accelerate the analysis and reporting of genomic alterations in oncology. We also introduce Velsera's completely reimagined solution to these challenges, CGW Plus, showcasing its variant quality assessment, clinical evidence review, and adaptive learning and memory capabilities.  

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August 10, 2024

RHEO In Action: A Snapshot of Innovation

Discover how users can effortlessly automate complex bioinformatics analyses with RHEO's push-button solution, designed to handle any use case or data modality. With seamless integration into existing external systems like cloud storage buckets, local databases, and LIMS systems, RHEO accelerates the pace of discovery, leading to faster, more profound insights into your data.

watch here
Group 8429
August 1, 2024

Expanding Your Research Horizons: Single Cell and Spatial Transcriptomics Capabilities in Biomedical Research

Discover how single-cell RNA sequencing and spatial transcriptomics are transforming our understanding of tissue cell diversity, developmental processes, and tumor heterogeneity.

watch here
CGW Plus webinar Social images
September 10, 2024
Tackling Complexity in Oncology Biomarker Interpretation with CGW Plus.

A discussion of challenges and innovative solutions in clinical genomics workflows. Discover how laboratories leverage variant databases and medical genomics knowledge to automate and accelerate the analysis and reporting of genomic alterations in oncology. We also introduce Velsera's completely reimagined solution to these challenges, CGW Plus, showcasing its variant quality assessment, clinical evidence review, and adaptive learning and memory capabilities.  

watch here
Single Cell Banner (YouTube Thumbnail) (2)
August 10, 2024

RHEO In Action: A Snapshot of Innovation

Discover how users can effortlessly automate complex bioinformatics analyses with RHEO's push-button solution, designed to handle any use case or data modality. With seamless integration into existing external systems like cloud storage buckets, local databases, and LIMS systems, RHEO accelerates the pace of discovery, leading to faster, more profound insights into your data.

watch here
Group 8429
August 1, 2024

Expanding Your Research Horizons: Single Cell and Spatial Transcriptomics Capabilities in Biomedical Research

Discover how single-cell RNA sequencing and spatial transcriptomics are transforming our understanding of tissue cell diversity, developmental processes, and tumor heterogeneity.

watch here
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