Access the latest technology today with flexible financing for instruments and reagents
All Kits & Reagents
Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep
All Selection & Planning Tools
Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price
All Software & Informatics Products
Integrated secondary analysis onboard the NovaSeq X System simplifies operations, accelerates the sequencing workflow turnaround
Fast, high-quality, sample-to-data next-generation sequencing services
All Popular Products
See what is possible through the latest advances in high-throughput sequencing technology
All Informatics Education
More About Us
Empower the next generation of scientists and engineers through educational opportunities and resources
More Career Info
All Investor Information
More Business Solutions
All Legal Information
Upgrade your MiSeqDx instrument from Windows 7 to Windows 10
All Support Tools
All Product Support Services
Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow
All Cancer Research Products
All Microbial Genomics Research
On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants
All Microbial Genomics Products
All Informatics Products
Sport sailors can use these environmental DNA collection kits even at full speed
All Agrigenomics Products
The institution is taking its research global, collecting international samples to find disease-associated variants
All Complex Disease Research Products
The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab
All Reproductive Health
All Reproductive Health Products
Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument
All Genetic Health Products
Learn how Illumina next-generation sequencing (NGS) works, and how it's furthering forensic science.
Find out how deep mitochondrial DNA (mtDNA) sequencing is being used to identify skeletal remains.
Fast library prep delivers quality de novo assembly of small genomes.
Instructions for human mtDNA D-loop hypervariable region sample preparation.
Instructions for human mtDNA genome sample preparation.
Improved human mtDNA analysis using NGS and cloud-based computing and storage.
Researchers use NGS to obtain more information-rich data and answer more complex forensic questions.
Criminalists use MiSeq FGx for high-resolution DNA profiling to build better forensic DNA databases.
Researchers identify genetic variants that influence facial features to enable facial imaging from DNA.
Learn about the advantages of targeted NGS and view the data validating the MiSeq FGx System in this Forensic Magazine article.
Learn about the potential of NGS to solve cold missing persons cases and identify unknown human remains.
In forensic work, the smallest detail can make the difference in solving a crime.
Hear from experts in the field how massively parallel sequencing (MPS) is paving the way ahead, and why now is the time to adopt it.
Learn how the Illumina forensic genomics workflow can transform forensic applications.
Dr. Mitch Holland of Penn State explains how NGS is helping us realize the power of mtDNA heteroplasmy.
The MiSeq FGx System is the first fully validated NGS solution designed exclusively for forensic science.