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Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep
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Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price
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DRAGEN v3.10 release now available, setting new standards for accuracy and increased genome coverage.
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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Whole-exome sequencing kit with library prep, hybridization reagents, exome probe panel, size selection beads, and indexes
Two DRAGENs help Cardio-CARE slay one petabyte of data to better understand heart disease in Hamburg
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Empower the next generation of scientists and engineers through educational opportunities and resources
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Get instructions for using Illumina DRAGEN Bio-IT Platform v4.0
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Enable comprehensive genomic profiling with accurate and comprehensive homologous recombination deficiency assessment
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Metagenomic and metatranscriptomic results from research on the microbiomes of an isolated tribe living deep in the Amazon
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A multi-species, low-cost, genome-wide genotyping platform to support molecular breeding in small grains
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Using whole-genome sequencing, a forward-looking organization is helping diagnose rare genetic diseases faster for more patients
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The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab
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Delivers a range of ready-to-use and custom panels for simple, flexible targeted resequencing that provides high-quality data you can trust.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, user-friendly workflow for a wide range of target enrichment applications encompassing custom panels, fixed panels, and whole-exome sequencing.
Perform targeted genotyping on large numbers of samples. Scale up to more than 1 million samples per year.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
Perform high-throughput, cost-effective genotyping for quality control, tracking, and stratification applications, including biobanking.
Purchase the TruSight Oncology 500 assay for the first time and receive an exclusive limited time offer.
Whole-genome sequencing library prep kits for small genomes (e.g. bacterial and viral genomes), amplicons, and plasmids.
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
This array offers an optimal and comprehensive set of both common and rare SNP content for diverse world populations.
Interrogate over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
Optimized chemistry to increase cluster density and read length, and improve sequencing quality scores, compared to earlier MiSeq reagent kit versions.
These sequencing reagent kits offer increased stability and robustness over the prior v2 kit version.