InnoviGene Suite

InnoviGene Suite is an all-in-one, browser-based platform that offers a symphony of Sanger sequencing and fragment analysis applications software, providing a harmonious bouquet of tools to connect, automate, and secure 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 capillary electrophoresis (CE) 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, improving your lab efficiency through a complete CE solution tailored for your needs.

Key features of InnoviGene Suite

Labs prioritize tools that simplify daily operations, save valuable time, support regulatory compliance, and offer top-level security. Software should be innovative, user-friendly, and adaptable, leveraging advancements like AI to enable true efficiency and keep pace with evolving technology.

  • Browser-based platform
  • Intuitive user interface
  • AI-based basecalling
  • Enhanced cybersecurity
  • Standards compliance
  • Data automation
  • Customizable reporting
  • Compatibility with CE workflow

InnoviGene Suite applications

InnoviGene Suite 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 incorporates the AI-based Smart Deep Basecaller, helping ensure precise and efficient data handling.

InnoviGene Suite 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
  2. To confirm the accuracy of the manufactured mRNA with specific changes

This application is highly applicable for plasmid sequencing, offering one-to-one matching.

STR typing comes with two modules:

  1. Sizing QC: Allows you to analyze a mixture of DNA fragments, separated by size
  2. Sizing Typing: Provides a profile of the separation, calculates the sizes of the fragments, and determines the alleles present in samples

Automated workflow for mRNA In Vitro Transcription

This application note presents a fully automated workflow for mRNA in vitro transcription (IVT), covering plasmid purification, template preparation, RNA synthesis, and purification. It highlights integrated quality control methods—including Sanger sequencing—to enable nucleic acid identity, purity, and quantification, with InnoviGene Suite playing a key role in analyzing and interpreting sequencing data to support reliable and efficient mRNA therapeutic development.

Optimize your capillary electrophoresis workflow with InnoviGene Suite

InnoviGene Suite optimizes CE workflows by integrating easily with CE consumables and SeqStudio Series instruments. The solution delivers higher data quality, with up to a 20% increase in read lengths—reaching up to 1200 base pairs—and improved quality values (QV) for generated data. It enables full automation through autoanalysis and template features, significantly enhancing workflow efficiency. Additionally, InnoviGene Suite is fully compatible with all CE instruments and workflows, helping ensure a smooth and consistent integration into existing laboratory processes.

For Research Use Only. Not for use in diagnostic procedures.