Access the latest technology today with flexible financing for instruments and reagents
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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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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
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See what is possible through the latest advances in high-throughput sequencing technology
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Empower the next generation of scientists and engineers through educational opportunities and resources
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Upgrade your MiSeqDx instrument from Windows 7 to Windows 10
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Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow
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On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants
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Sport sailors can use these environmental DNA collection kits even at full speed
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The institution is taking its research global, collecting international samples to find disease-associated variants
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The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab
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Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument
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Find tools to help you choose the right products for your needs and plan your experiments. Identify the right library prep kit or microarray, calculate sequencing coverage, explore methods compiled from publications, design custom assays, and more.
This guide contains an overview of instrument components and instructions for operating and maintaining the MiniSeq System.
Sequencing coverage describes the average number of NGS reads that align to known reference bases. Coverage requirements vary by application.
Additional information about sequencing quality scores, how they are calculated, and the relationship between quality score and base call accuracy.
The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.
Discover how the simple, affordable MiniSeq System makes sequencing an everyday tool for labs of any size.
Mattia Prosperi, PhD, will use his MINI Cooper and MiniSeq to study the spread of mosquito-borne pathogens in Florida.
Hongmei Li-Byarlay, PhD, describes how she will use the MiniSeq to study the honeybee.
Una McVeigh discusses how the MiniSeq System will help her identify new genetic variants associated with breast cancer.
This webinar provides an introduction to the MiniSeq System and its simple, streamlined workflow.
Learn how comprehensive tumor profiling with NGS can help you avoid costly and time-consuming iterative testing.