一个fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbes.
一个n economical solution for sequencing RNA from FFPE tissues and other low-quality samples.
一个chieve 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.
Identify genetic associations with common and rare traits across diverse populations.
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.
The first FDA-approved NGSin vitrodiagnostic for metastatic colorectal cancer for use in establishing eligibility of patients for treatment with Vectibix®.
FDA-cleared next-generation sequencing assay provides a full view of coding regions of the CFTR gene, to aid in in vitro diagnosis of cystic fibrosis.
FDA-cleared NGS assay with the largest panel of clinically relevant, functionally validated cystic fibrosis variants in a diverse population.
Comprehensive 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.
一个ssay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
一个n economical and powerful computing environment to manage, analyze, and share data.
一个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.