Modular design for maximum compatibility
Choose all three integrated modules or select only what you need.

What’s inside

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.
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.

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
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
Key benefits

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

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
Stay at the forefront of newborn genomics
Featured resources
*1-3 day estimation is based on usage of non-specialized genetic interpretation software.
