Reveal new connections in complex disease

Reach further with NGS and array solutions

Complex Disease Genomics

Complex diseases affect us all. Illumina is committed to advancing our understanding of complex diseases and how they will be diagnosed and treated.

Complex diseases result from a combination of genetic and environmental factors, many of which are not understood. These diseases include neurodegenerative, psychiatric, and autoimmune disorders, and others.

The expanding Illumina complex disease product portfolio includes array and next-generation sequencing (NGS) technologies that are helping drive a revolution in complex disease genomics. Complete solutions deliver high-quality, reproducible results that accelerate research on various complex diseases. These discoveries have the potential to lead to life-changing improvements for patients and their loved ones.

Array and NGS soultions for Complex Disease Genomics

Illumina offers microarray and NGS solutions to advance complex disease research in all focus areas, from immunology to neuroscience and beyond.

Immunology Research
Neuroscience Research
Other Complex Disease Research
See All

Illumina provides genomic solutions for all levels of complex disease research, from large-scale genomic discovery to functional cellular and clinical research.

Cellular Research
Clinical Complex Disease Research
High-Throughput Genomics Research
See All
Genomic Solutions for Cell Biology and Complex Disease Research

This review gives a general overview of how genomic technologies and NGS can help in the study of complex diseases, and highlights recent publications featuring Illumina technology.

Read Publication Review
Genomic Solutions for Cell Biology and Complex Disease Research
Interested in receiving newsletters, case studies, and information on complex disease genomics? Please enter your email address.
NGS for Cell Biologists
An Introduction to NGS for Cell Biologists

Learn the numerous ways that genomic technologies can be applied to tumor biology.

Access PDF
Genomic Basis of Complex Disease
Methods for Investigating the Genomic Basis of Complex Disease

Learn how genomics can provide a deeper understanding of complex diseases.

Access PDF
NextSeq 500 System
Unraveling Disease Mechanisms with the NextSeq 500 System

Researchers are studying mtDNA, piRNA and TCR repertoire diversity to unlock the secrets of cancer, infertility, and autoimmune disease.

Access PDF
Mapping Neural Diversity with Single-Cell mRNA-Seq
Mapping Neural Diversity with Single-Cell mRNA-Seq

The ability to analyze gene expression signatures from individual cells is transforming the way neurons are classified.

Read Interview
Driving IBD Discovery with Integrative Genomics
Driving IBD Discovery with Integrative Genomics

Dr Carl Anderson discusses integrated genomic research approaches in inflammatory bowel disease (IBD) research.

Watch Video
Driving ALS Discovery with Integrative Genomics
Driving ALS Discovery with Integrative Genomics

Jan Veldink, PhD shares how integrative genomics helped drive his ALS research, leading to the discovery that NEK1 is an ALS gene.

Watch Video
NGS for Cell Biologists
Complex Disease Applications Brochure

Explore applications, methods, and streamlined workflows to power discovery in complex disease research.

Access PDF
The Functional Effects of Genetic Variants
The Functional Effects of Genetic Variants

Tuuli Lappalainen, PhD is working toward identifying how genetic differences may affect an individual’s risk for certain diseases.

Watch Video