InnoviGene Suite

A unified platform solution

InnoviGene Suite is an all-in-one, browser-based platform that offers a suite of Sanger sequencing applications software, providing a harmonious bouquet of tools to automate and optimize your data analysis. With its user-friendly interface and advanced features, InnoviGene Suite orchestrates researchers and scientists to efficiently manage and analyze their sequencing data, enabling accurate and reliable results.

Experience the power of innovation with InnoviGene Suite and let it help you take your sequencing workflow to new heights of productivity and success. Unleash the melody of discovery as you immerse yourself in the harmonious rhythm of InnoviGene Suite's capabilities.

Key features

Browser based platform

This allows multiple users in the lab to access the software simultaneously from any location, sharing the same data and protocols for collaborative and efficient work.

Data automation

Streamline and optimize your sanger data analysis leveraging automated features (quality control, confirmation, mismatch detection) for improved efficiency and accuracy.

Additional data security/privacy

Safeguard your sensitive information and support user privacy with robust data security measures and privacy protocols.

21 CFR Part 11 & GMP compliance support

Support compliance to 21 CFR Part 11 through a dedicated console (Security, Audit, e-signature) that enables electronic records , users management, tracking and monitoring of processes.

Customizable reports: allows users to tailor the presentation of your data (quality control, mismatch detected, detected) to their specific needs, thereby enhancing the clarity and relevance of the information presented.

OS compatibility Windows 11: enables simple operation and user experience across current operating system platforms.

AI Based basecalling: leverages advanced machine learning algorithms to accurately identify nucleotide sequences, hence supporting the precision and efficiency of data analysis and reducing needs of resequencing for difficult samples.

Minimal training: designed with an intuitive user interface, requiring minimal training, thus enabling users to quickly grasp its functionalities and start using it effectively.

Intuitive user interface: Experience a smooth and intuitive user interface, simplifying navigation and supporting productivity for sanger sequencing data analysis and management.

InnoviGene Suite modules and applications

InnovieGene Suite is a comprehensive solution providing two sequencing modules, Sequencing QC and Sequence Identity, enabling Sanger sequencing applications, including sequence confirmation and mRNA QC. It is installed on a local PC, offering access from devices connected to the local network.

Sequencing QC module

This module is designed for scientists who require a straightforward analysis and review of their sequence and its quality metrics. It allows you to explore data, make edits, print out QC reports, and extract sequences. It is an ideal tool for biopharma, clinical organizations, service providers, or core labs providing sequence to end users and for anyone who needs to generate a report in a user-friendly way. The Sequencing QC module incorporates the AI-based Smart Deep Basecaller.

Sequence Identity module

This module is designed for precise specimen sequencing confirmation. For every specimen you want to sequence, you provide the software with a reference, and it generates a list of mismatches. This feature is particularly important for mRNA QC manufacturers for two reasons: 1) to identify the specimen's characteristics, and 2) to confirm the accuracy of the manufactured mRNA with specific changes. This module is highly applicable for plasmid sequencing, offering one-to-one matching.

Optimize your capillary electrophoresis workflow with InnoviGene Suite

The InnoviGene Suite is compatible with our Applied Biosystems capillary electrophoresis instruments and consumables.

Automated data analysis

InnoviGene Suite and our SeqStudio Flex Genetic Analyzer together offer automation of data analysis through the Auto-analysis & Template feature. This allows easy loading of AB1 files generated by the SeqStudio Flex system into a local folder. InnoviGene Suite then manages, processes, and analyzes the files, resulting in efficient data and report generation. This automation helps improve workflow efficiency, leading to faster turnaround times and higher overall efficiency in data analysis.

Longer read lengths

InnoviGene Suite complements the benefits of the BigDye Terminator sequencing kit by enhancing data quality and reducing the need for resequencing. Indeed, leveraging the InnoviGene Suite AI-based basecaller helps deliver higher QC and extend read lengths by 20% (up to 1200 bp).