75 breakthrough innovations and our simplest workflow yet
Kits & Reagents
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility
Selection & Planning Tools
Compare instruments and find one that's right for you
Software & Informatics Products
Pay-as-you-go or purchase larger quantities at a lower price point for high-throughput data analysis applications
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
Find popular product groupings for your workflow
Whole-genome shotgun sequencing and transcriptomics provide data to refine drug discovery and development
Love and care is never rare
All Investor Information
After a shutdown: best practices to ensure a successful reopening
All Support Tools
Product Support Services
Expanded portfolio enables comprehensive genomic profiling from blood and tissue
Cancer Research Products
Microbial Genomics Research
Whole-genome sequencing using NGS technology delivers comprehensive genetic analysis
Microbial Genomics Products
A highly sensitive and accurate tool for measuring expression across the transcriptome
Powerful tools for studying the transcriptome in an unbiased manner from minimal input
Complex Disease Research Products
How cfDNA affects test results when considering NIPT
Reproductive Health Products
Genetic Health Products
Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.
Genet Med 18 231-8 2016
Clinical Sensitivity of Cystic Fibrosis Mutation Panels in a Diverse Population.
Hum Mutat 37 201-8 2016
Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic Fibrosis.
J Mol Diagn 18 267-82 2016
Information about instrument components and software, performing a sequencing run, and maintenance.
Preparing a lab for the MiSeqDx Platform: lab space, electrical, and bench requirements, and user-supplied consumables.
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.
User guide, safety guide, site preparation guide, and related application and tech notes for the MiSeqDx instrument.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.
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