High-throughput genomic analysis tools

Fast, cost-effective sequencing and microarray solutions for large-scale studies

High-Throughput Genomics

Researchers are harnessing the power of high-throughput genomics to conduct large-scale, global genetic analyses. This research often focuses on multifactorial genetic discovery of disease risk markers, and may involve looking for changes in genetic variants such as single nucleotide polymorphisms (SNPs), indels, splice variants, structural variants, and methylation markers.

High-throughput genomics studies with tens to hundreds of thousands of samples require fast, cost-effective tools. Illumina offers high-throughput genomic analysis technologies with comprehensive sample-to-analysis solutions and exceptional collaborative expertise to meet these needs.

Sequencing by synthesis is a massively parallel sequencing technology that has launched the next generation in genomic sciences.

Our high-density microarray technology offers trusted data quality and exceptional coverage of valuable genomic regions, making Illumina arrays the platform of choice by leading institutions for high-throughput screening and large-scale genotyping research programs.

Scientist in a High-Throughput Lab Using Illumina Sequencers

Recent advances in sequencing technologies have allowed for the development of high-throughput genomics-based strategies to assay GWAS SNPs for potential functional relevance. Powerful combinations of high-throughput experimental assays, single-cell approaches, and computational analyses are accelerating the ability to link variants to function, and, by extension, link genotype to phenotype.

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Prioritizing Functional Genetic Variants
Library Prep Automation

For labs preparing large quantities of NGS libraries, liquid-handling robots and other automation solutions provide a good option.

Multiplex Sequencing

Sample multiplexing allows large numbers of NGS libraries to be pooled and sequenced simultaneously during a single run.

Bioinformatics Pipeline Setup

Find information and resources to help simplify the process of setting up an informatics infrastructure and data analysis pipeline.


Learn how you can benefit from a laboratory information management system (LIMS) optimized for genomics, and find out what to look for.

High-Throughput Genotyping

Large-scale genotyping with arrays can identify variants associated with disease risk in large cohorts or populations.

High-Throughput Sequencing

Process more samples to improve statistical power. Get multidimensional insights and increase analytical resolution in a scalable, cost-effective manner.

Hear From High-Throughput Genomics Labs

Establishing and Scaling an Efficient Genotyping Facility
Establishing and Scaling an Efficient Genotyping Facility

Prenetics created a high-throughput genotyping laboratory to serve its growing customer base in Southeast Asia.

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DNA Variants
Identifying Breast Cancer Targets

The Breast Cancer Atlas Project involves cellular genomics studies of over a million individual breast cancer cells to help researchers identify potential therapeutic targets.

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Scientists in a High-Throughput Lab
Scaling Up to Genotype Thousands of Samples

Resource planning and automated genotyping workflows allowed GPBio to achieve immediate efficiency and throughput gains.

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Population Genomics

National population genomics programs seek to integrate large, diverse data sets, combining clinical information with genomic data at scale.

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Complex Disease Genomics

Genomic technologies are introducing new avenues for understanding complex disease etiology on a molecular level.

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Drug Discovery & Development

NGS can help pharmaceutical scientists identify potential drug targets and support development of targeted therapies.

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Genome-Wide Association Studies
Genome-Wide Association Studies

These studies use high-throughput genomics to quickly scan entire genomes, to find genetic variants linked to a disease or trait. 

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