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Flyer
Newborn Health - Working with Revvity
Revvity's comprehensive solutions and services for newborn health betterment.
Flyer
Official gene panel flyer
Summary of Revvity NGS gene panel used for newborn DNA sequencing research in the laboratory.
Infographic
Newborn sequencing research with Revvity
Infographic highlights Revvity's newborn sequencing workflow, featuring 390+ genes, for advancing genomic research while simplifying laboratory processes.
Flyer
The future of NGS software
A modular NGS software suite with LIMS, DNA analysis, and interpretation tools, designed to enhance genomic research workflows.
Brochure
Software suite for NGS research
A modular, customizable software suite for genomic analysis, enhancing NGS research with LIMS, DNA analysis, and interpretation tools.
Application Note
Targeted sequencing of DNA from dried blood spot samples
Optimized workflow for targeted sequencing of DNA from dried blood spots, ensuring high-quality genomic data for research applications.
Flyer
NGS software specifications
A secure, cloud-based NGS software suite with LIMS, DNA analysis, and interpretation tools, ensuring data confidentiality and integrity.
Technical Note
Technical Note NeoBase 2 on Sciex Triple Quad 4500MD - digital
Technical note NeoBase 2 on SCIEX Triple Quad 4500MD LC-MSMS System Digital.pdf
Guide
Example Report for PG-seq Core Panel
This report is an example of the output from utilizing the software associated with the PG-seq Core Panel.
Product Info
PG-Seq Core Panel HG38 Bedfile
The BED file for the PG-Seq™ Core Panel defines the genomic regions analyzed, focusing on over 200 SNPs located 2 Mb upstream and downstream of eight commonly targeted genes associated with monogenic disorders, covering a total of 4 Mb.
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