GENOVESA

The ultimate genomic solution

Designed for efficient clinical decision-making.

Streamline your NGS workflow

Whether you're analyzing small panels or conducting whole-genome sequencing, GENOVESA will meet any need with its powerful, customizable tools.

From data quality control to personalized variant interpretation, GENOVESA streamlines your workflow for efficient and accurate results.

All in one solution

from raw data to clinical reports in one platform
handle large datasets with cloud-based efficiency
GDPR-compliant with end-to-end encryption
tailor databases, reports, and workflows to your needs
connect with existing LIS and bioinformatic tools
share and interpret data across clinics effortlessly

Key features of GENOVESA

User-friendly interface

Discover the interface for easy data exploration, interpretation, and visualization, effortlessly identifying patterns.

Automated data analysis

Automated data analysis allows you to effortlessly process large datasets with precision and efficiency.

Advanced features

GENOVESA caters to experienced users with options to adjust parameters, apply complex filters, and visually evaluate variants.

Quality control

GENOVESA software ensures data quality with advanced quality control measures, including features such as Global Mapping Quality and fastQC.

Clinical variants database and data sharing

Own variant database.
Internal variant interpretation.
Data sharing between clinics.

Clinical report generation

Effortlessly generate clinical reports and streamline your reporting process.

Compatible with multiple sequencing technologies

GENOVESA is compatible with a wide range of sequencing technologies, including Illumina, MGI, PacBio, Oxford Nanopore Technologies, Genapsys, and others.
This flexibility allows users to analyze data regardless of the sequencing platform used.

Master NGS data effortlessly

GENOVESA is intuitive and easy to use. For beginners in NGS analysis, it allows a quick and easy generation of relevant information of their NGS data, without the need of their own dedicated bioinformatic experts.

On the other hand, GENOVESA allows experienced users to adjust and modify parameters, use complex filtering rules, and visually evaluate variants at the individual reading level.

Fast interpretation

The platform automates the entire process, from raw sequencing data (FASTQ files) to generating clinical reports.

This ensures rapid, accurate, and streamlined analysis, allowing users to focus on interpretation rather than technical details.

Comprehensive data management

All sequencing data, including small panels, clinical exomes (CES), and whole-exome (WES) or whole-genome (WGS) data, can be stored and easily managed in one place.

The system allows for efficient filtering, visualization, and classification of variants, which can be shared between clinics for collaborative evaluation.

Data security and GDPR compliance

GENOVESA prioritizes data security with HTTPS encryption and stores data in a secure data center in Prague.

The platform is fully compliant with GDPR regulations, ensuring the privacy and protection of sensitive patient information.

Advanced quality control

The platform includes sophisticated quality control measures for sequencing data (FASTQ, BAM, VCF), ensuring that users can trust the accuracy and reliability of their analyses.

Additionally, customizable filters allow for the exclusion of sequencing errors based on frequency across experiments.

More reasons to choose GENOVESA

Customizable annotation databases

Access a wide range of annotation databases and easily expand or customize them to fit your specific needs. GENOVESA offers flexibility for all types of genetic analyses, from small panels to whole genome sequencing.

Integration with laboratory information systems (LIS)

Seamlessly integrate with existing LIS systems for smooth data import and export. This feature enhances workflow efficiency, making GENOVESA ideal for clinical and research settings.

Collaborative variant interpretation

Facilitate teamwork by sharing data across clinics. GENOVESA allows users to collaboratively interpret genetic variants, improving both diagnostic accuracy and speed.

Flexible interpretation

Create customized clinical reports with tailored variant interpretation, comments, and classifications. This flexibility ensures precise and personalized reporting for both clinical and research applications.

Training and support services

Get continuous support with access to training courses, tutorials, and user assistance. GENOVESA ensures you get the most out of the platform, reducing the learning curve and ensuring success.

Fast and scalable performance

Leverage GENOVESA’s cloud-based architecture for rapid data processing. The platform scales with your growing data needs, ensuring efficient performance at any project size.