A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbes.
An economical solution for sequencing RNA from FFPE tissues and other low-quality samples.
Achieve up to 15 Gb of output with improved cluster density, read length, and quality scores.
These reagents offer increased stability and robustness over the v2 kit version.
Find the system that's right for you and your lab. Explore the entire porfolio of Illumina sequencing systems and microarray scanners.
View All InstrumentsDetermine the best kit for your needs based on your project type, starting material, and method of interest.
From fast and flexible to ultra-high-throughput production power, find the NGS system that's right for you.
Use this tool to explore experimental sequencing library preparation methods compiled from the scientific literature.
Interrogate over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
This microarray combines exceptional coverage of clinical research variants with optimized multi-ethnic, genome-wide content.
Perform production-scale targeted genotyping studies on any species with user-defined content.
GSA is a next-generation genotyping array for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research.
We offer a variety of next-generation sequencing products intended for in vitro diagnostic use. Browse our catalog and find the product that fits your needs.
View All IVD ProductsComprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
Study gene expression, variants, and fusions for 1385 oncology genes, in all RNA sample types, including FFPE.
Comprehensive panels targeting disease-associated regions of the exome with high analytical sensitivity and specificity.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Provides ultra-rapid secondary analysis of next-generation sequencing (NGS) data.
An economical and powerful computing environment to manage, analyze, and share data.
A laboratory information management system that helps labs track samples and optimize procedures and workflows.
Verify instrument operation and obtain an audit-ready report to help meet regulatory requirements.
Evaluate sample quality and repair degraded FFPE DNA samples for use in Infinium array-based assays.
Unique barcodes to seamlessly track samples through the sequencing workflow.