Start Your Evaluation
See how the VarSeq Suite fits your workflows with your data, your clinical applications, and zero IT setup required.
How It Works
Our structured evaluation process is designed to minimize your overhead while maximizing your team's exposure to the platform's clinical capabilities.
Discovery & Deployment Call
We start by understanding your current NGS workflows, pipeline challenges, and clinical goals. Together, we'll walk through on-prem, private cloud, and hybrid options to identify the right fit for your infrastructure and compliance requirements.
Scope Your Applications
Tell us what you're focused on so we can tailor the evaluation to what matters most—from hereditary disease to somatic oncology.
Dedicated Evaluation Environment
We provision a ready-to-use environment for your team: no internal IT setup, no infrastructure prerequisites. You log in and start.
Bring Your Data or Use Ours
Run your own validation samples through real workflows. If you're early in your NGS journey, we'll provide curated public reference datasets matched to your clinical applications.
Training & Guided Validation
Our customer success team works alongside you to ensure your evaluation goals are met from configuration through final validation results.
What You'll Walk Away With
Hands-on experience running your target clinical workflows
Validation evidence using your own samples or established reference data
A clear understanding of deployment, integration, and scaling path
Confidence that results meet your expected performance benchmarks
"Our goal is to ensure that by the end of your evaluation, you have a fully validated workflow ready for clinical production."
Support for Every Clinical Application
The VarSeq Suite is designed to support a wide range of clinical and research focus areas, from configuration through final validation results.
Rare Disease Diagnosis
Support for trio and extended family analysis with de novo, compound het, and phenotype-based variant prioritization.
Precision Oncology
Automate the interpretation of somatic variants using AMP guidelines, integrating therapy matching and clinical trial search.
Hereditary Disease Risk
Comprehensive workflows for inherited risk analysis, supporting high-throughput screening and clinical reporting.
Prenatal & Carrier Screening
Partner-paired workflows for reproductive risk analysis, supporting autosomal and X-linked recessive disorder screening.
Pharmacogenomics
PGx star allele calling and diplotype determination with CPIC guidelines for personalized medicine.
Variant Interpretation
Guided ACMG/AMP classification with automated criteria recommendation and evidence gathering in VSClinical.
Ready to Scale Your Genomics Program?
Connect with our team to architect the right licensing and deployment model for your bioinformatics infrastructure—typically scoped within one call.