75 breakthrough innovations and our simplest workflow yet
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Streamlined high output single-cell sequencing on your benchtop
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A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
Software & Informatics Products
Bringing efficiency and high confidence to case management, variant analysis, and interpretation in rare disease
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
Find popular product groupings for your workflow
Empower the journey from association to causality
Joins Africa CDC alongside the Bill & Melinda Gates Foundation and others in a four-year plan
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Windows 10 upgrades and Windows 7 ESU licenses available for Illumina systems
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Expanded portfolio enables comprehensive genomic profiling from blood and tissue
Cancer Research Products
Microbial Genomics Research
Highly sensitive detection and characterization of common respiratory viruses, including COVID-19 strains
Microbial Genomics Products
2020 Agricultural Greater Good Initiative Winner shares how grant will improve crop yield and insect resistance
Studying populations and groups helps us understand how variants relate to each other and various diseases
Complex Disease Research Products
Endorsement from ACOG opens doors for pregnant women of any age or risk
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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