Highly tunable data output to run virtually any genome, sequencing method, and scale of project
Kits & Reagents
Easy adoption with superior support across the entire workflow. Fast, simple library prep and enrichment workflow from Illumina.
Selection & Planning Tools
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
Enables and accelerates research leveraging BaseSpace Correlation Engine
Environmentally friendly packaging reduces waste from landfills and carbon emissions
All Investor Information
Three approaches to help researchers with sequencing
All Support Tools
Product Support Services
Expanded portfolio enables comprehensive genomic profiling from blood and tissue
Cancer Research Products
Microbial Genomics Research
This high-throughput NGS test detects SARS-CoV-2 in nasopharyngeal, oropharyngeal, and mid-turbinate nasal swabs
Microbial Genomics Products
A transformational approach to biodiversity monitoring
New library prep kits enhance research in rare genetic diseases
Complex Disease Research Products
Why he believes CGP is poised to become a standard of care in oncology
Find out why laboratories In Europe have implemented VeriSeq 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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