Newborn Sequencing Research
With the latest advancements in next generation sequencing (NGS), we are experiencing rapid acceleration in genetic disease research. While NGS maintains the power to detect genetic variants responsible for many diseases, these technologies have been inaccessible for many laboratories.
Through our decades of experience in rare disease technologies, Revvity has developed an end-to-end NGS workflow to suit your needs. Our customizable, holistic workflow – from the DNA extraction of dried blood spot samples, library preparation, automated liquid handling, sequencing, to final data analysis – is built to bring newborn research into the hands of more laboratories. One end-to-end solution from one supplier.
For research use only. Not for use in diagnostic procedures.
Benefits for your laboratory
See how you can power your newborn sequencing research with Revvity today.
Workflow steps
From sample to final result, we cover the entire sequencing process.
Sample collection
226 Sample Collection Device
226 Sample Collection Device
A dried blood spot card that delivers reliable and homogenous analytical results from across the dried sample area. Enables simplified sample collection and delivery.
Laboratory LIMS
Revvity Genomics LIMS
Revvity Genomics LIMS
Our cloud-based, platform solution is primed for secure data management and LIS integration. The solution operates on ISO27001 certified cloud technology while the application is designed to comply with GDPR and HIPAA requirements.
Sample extraction
Multiple Options
Multiple Options
Revvity Puncher Instruments
Simplified and robust options for your DBS (dried blood spot) punching needs. Equipped with semi-automatic punching capabilities and a changeable head, punch DBS samples into microtitration plates with ease.
Chemagen 360 Instrument & Kits
Chemagen’s well-established magnetic bead-based technology brings reliability to sample extraction. Chemagen is optimized for extracting high-quality and high-yield genomic DNA from dried blood spot samples, making it the perfect choice for newborn sequencing research.
Sample QC and quantification
Multiple Options
Multiple Options
With a host of solutions, we offer several reliable systems that are designed to quantify and assess the quality of your DNA samples. Get fast, high-throughput QC analysis of your samples.
Library preparation
NEXTflex® Kits
NEXTflex® Kits
Offers robust genome coverage to identify variants in 390+ genes. Targeted regions are designed for comprehensive research of early onset disorders. Library prep is also Illumina® and Element Biosciences compatible.
Library preparation automation
Multiple options
Multiple options
With a portfolio of automated liquid handling solutions, Revvity offers flexibility and throughput to meet your needs. Our instrumentation is designed to minimize cross-contamination and user error.
- Sciclone G3 NGSx Workstation
- Zephyr Workstations
- Janus Workstations (for normalization)
Library QC and quantification
Multiple options
Multiple options
With a host of solutions to serve your unique needs, Revvity delivers fast, high-throughput QC analysis of NGS libraries. Enables a simplified approach to DNA fragment analysis, including NGS library QC.
Sequencing
Element Biosciences AVITI™ and Illumina®
Element Biosciences AVITI™ and Illumina®
Compatible library with AVITI sequencers and Illumina platforms. With unparalleled performance, the cost-effective AVITI system reimagines sequencing with your needs in mind. Built for fast turnaround time, the AVITI benchtop sequencer can complete a 2x150 run with indexing, generating up to 600 GB of data and 2 billion reads.
Primary and secondary analysis
Revvity Genomics Analyze
Revvity Genomics Analyze
Built to offer a seamless fit to your analytical needs for sequencing data, our software offers alignment and variant calling to your laboratory. Software operates on the same closed & secure platform as our LIMS solution and is compatible with both Element Biosciences and Illumina sequencers.
Tertiary analysis and reporting
Revvity Genomics Interpret
Revvity Genomics Interpret
Our software enables easy result interpretation for your research needs. Preview, add comments and select your report delivery method, all in-app. A cloud-based application, users can login from anywhere for easy access reporting. Software operates on the same closed & secure platform as our LIMS solution.