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Revvity Genomics Software

Redefining what's possible in genomic research

Genomic analysis can be complicated, but your software shouldn't be.

Simplify your science with our cloud-based informatics suite – purpose-built for newborn screening and genomic laboratories, trusted throughout Revvity's global laboratory network.

Introducing the Revvity™ Genomics Software. It's time to redefine sequencing research.

For research use only. Not for use in diagnostic procedures.

Revvity Genomics Software

 

Modular design for maximum compatibility

Choose all three integrated modules or select only what you need.

Revvity genomics software
Harmonized sample management

Harmonized sample management

With the LIMS module, efficiently manage sample intake with precise accessioning and complete traceability throughout the sample journey. Strategic QC checkpoints ensure quality, allowing immediate exclusion of failed samples to preserve downstream integrity of your results.

Intelligent data processing

Intelligent data processing

The Analyze module combines next-generation sequencing analysis with cloud-based parallel processing to eliminate bottlenecks. Compatible with Element and Illumina sequencers, our user-friendly interface replaces complex bioinformatics environments with an intuitive dashboard. This empowers your team while maintaining compatibility with your current sequencing infrastructure.

Exact genomic interpretations

Exact genomic interpretations

The Interpret module transforms your sequencing data into meaningful, actionable insights with powerful pre-filtering capabilities and pre-classifications. These features are designed to create workflow efficiency - compressing interpretation timelines from several days to less than 2 hours, all while leveraging our continuously curated database of 390+ genes.

What’s inside

Comprehensive gene panel

Comprehensive gene panel

Our targeted gene panel provides thorough coverage for newborn sequencing research, ensuring you have access to all critical genetic markers. Each included gene meets rigorous selection criteria established by our team of genomic experts and bioinformaticians.

About our panel

Our targeted gene panel provides thorough coverage for newborn sequencing research, ensuring you have access to all critical genetic markers. Each included gene meets rigorous selection criteria established by our team of genomic experts and bioinformaticians.

About our panel

Accelerated variant interpretation

Accelerated variant interpretation

Engineered by laboratory specialists, our signature set of in-module capabilities is designed to shrink variant assessment times from 1-3 days to below 2 hours.*

Engineered by laboratory specialists, our signature set of in-module capabilities is designed to shrink variant assessment times from 1-3 days to below 2 hours.*

Accessible reporting suite

Accessible reporting suite

Generate tailored reports that adapt to your established workflows rather than forcing you to adapt to existing software templates . Create high-volume and automated reporting for benign variants or easily classify pathogenic variants within one intuitive workspace using a host of assay-specific templates.

Generate tailored reports that adapt to your established workflows rather than forcing you to adapt to existing software templates . Create high-volume and automated reporting for benign variants or easily classify pathogenic variants within one intuitive workspace using a host of assay-specific templates.

Take a closer look

Discover the modular and configurable software suite designed to propel your genomic analysis.

Key benefits

Operational excellence
Operational excellence

Reduce complexity and save valuable time with intelligent automation and parallel processing via cloud, designed to covert days of work into hours – allowing your team to focus on what matters most.

Uncompromising accuracy
Uncompromising accuracy

Paring strategic and multi-layered quality control checkpoints alongside a continually curated genomic database ensures reliable results that you can trust.

Seamless adaptation
Seamless adaptation

Configure the platform to your existing workflow and integrate with your preferred sequencing technology, offering true flexibility without forcing you to conform to rigid constraints.

Your partner in genomic excellence

With our reputable software suite and sequencing workflow, Revvity's list of genomic collaborations continues to grow. See what's possible – read about two of our latest projects here.

Stay at the forefront of newborn genomics

Join our community of leading laboratories by subscribing to our newborn sequencing eNewsletter. Packed with the latest insights and developments in newborn genomic research.

*1-3 day estimation is based on usage of non-specialized genetic interpretation software.

Revvity AI Assistant Beta