GENOVESA software

GENOVESA

Bioinformatic software
for all NGS data

From FASTQ to report in one streamlined bioinformatic pipeline

Fast

From FASTQ to report in one streamlined bioinformatic pipeline

From FASTQ to report in one streamlined bioinformatic pipeline

Secure

Cloud-native & compliant with GDPR

From FASTQ to report in one streamlined bioinformatic pipeline

Intuitive

Clinician-friendly interface, zero clutter

From FASTQ to report in one streamlined bioinformatic pipeline

Comprehensive

One platform for all your NGS diagnostics:

Germline

Germline

Somatic

Somatic

Metagenomic

Metagenomic

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At BioVendor, we believe clinical genomics should be clear, consistent, and ready for action.

That’s why we built GENOVESA — a secure, end-to-end platform for automated variant interpretation, reproducible analysis, and seamless clinical reporting.

From amplicons and targeted panels to WES, WGS, or other DNA/RNA-seq data, GENOVESA transforms raw sequencing into meaningful, clinical-grade insights — fast.

Compatible with Illumina, Oxford Nanopore, MGI, Element, PacBio, Genapsys, and more, GENOVESA brings reproducibility to every run and confidence to every call — no scripts, no guesswork.

Try our platform

Request a customized demo or get answers to your specific questions.

Synergy of two established companies

As experts from BioVendor Group and Bioxsys, we developed GENOVESA, a cloud-based bioinformatic software for NGS data analysis.

At BioVendor Group, we ensured the software addresses the needs of clinical and research labs, while Bioxsys provided bioinformatic expertise for precise data interpretation.

Together, we created an easy-to-use, all-in-one solution simplifying NGS analysis for laboratories worldwide.

company logo BioVendor Group
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The BioVendor Group in numbers

30+

Years of clinical
excellence

180+

People ​in research ​and development

115+

Countries ​represented ​by companies

You already know our NGS solution.
How will it help your lab?

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  1. Increased Efficiency and Accuracy: Our NGS solution speeds up sample analysis, improving workflow efficiency and reducing diagnostic time.

  2. Simplified Data Interpretation: Gain access to advanced analysis tools, making complex genetic data easier to interpret.

  3. Reduced Operational Costs: Optimize sequencing processes, cutting down on costs while increasing sample throughput.

  4. Flexibility for Your Needs: Tailor analyses to your lab’s specific focus, from oncology research to genetic counseling.

  5. Support and Training: We provide comprehensive training and support to help your team maximize the solution’s potential.

  6. High Quality and Reliability: Trusted globally, our solution ensures reliable, high-quality results for your lab.

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