Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project
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P1 reagents are now available for NextSeq 1000/NextSeq 2000 Systems, offering added flexibility to meet your project's needs
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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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Sequencing and microarray products for diverse applications
See what is possible through the latest advances in high-throughput sequencing technology
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How artificial intelligence and automation are enabling precision medicine to become the standard of care
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Manage the security and set up networking for your sequencing system
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Enable comprehensive genomic profiling with accurate and comprehensive homologous recombination deficiency assessment
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Monitor SARS-CoV-2 variants and other respiratory viruses in the community
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Mapping genetic diversity to identify where confiscated gorillas come from and boost survival rates
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Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation
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Comprehensive, IVD, in-lab aneuploidy screening solution for accurate NIPT results in 26 hours
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Whole-genome sequencing (WGS) for rare disease offers key advantages over other genetic testing methods
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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.
Access the MiSeq System interactive guide for general use, troubleshooting, and other additional resources.
Information about instrument components, software, required products, performing a sequencing run, and instrument maintenance.
Find lab specifications and requirements for preparing your lab for a MiSeq System.
Online Illumina sequencing courses are free, interactive, and available any time.
This tool will help you determine the best hands-on sequencing training for your needs based on your area of interest, application, library preparation kit, and platform.
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.
Find system guides, related application and technical notes, and other supporting documentation for the MiSeq System.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.
The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.
Practical information for new MiSeq users with many tips, tricks, and microbial examples gleaned from long instrument experience.
Researchers used paired-end 16S amplicon sequencing on the MiSeq System to explore their microbe-cycling hypothesis.
Researchers compared viral RNA sequences from samples, and found substitutions absent from other Western African Ebola genomes.