High-throughput genomic analysis tools

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

High-Throughput Genomics: NGS & Arrays

Researchers are harnessing the power of high-throughput next-generation sequencing (NGS) and microarray technologies 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 sequencing and array technologies with unprecedented sample-to-analysis solutions and unparalleled collaborative expertise to meet these needs.

Illumina sequencing by synthesis (SBS) is a massively parallel sequencing technology that has revolutionized sequencing capabilities and launched the next generation in genomic sciences. The latest Illumina sequencers unite high-performance imaging with state-of-the-art flow cells to deliver massive increases in throughput.

Scientist in a High-Throughput Lab Using Illumina Sequencers

With unmatched scalable throughput, tremendous flexibility for a broad range of applications, and streamlined operation, the NovaSeq 6000 System is the most powerful high-throughput Illumina sequencer to date, perfectly positioned to help scientists perform large-scale genomics studies. The system offers output of up to 6 Tb and 20 billion reads in < 2 days.

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NovaSeq Instrument and Flow Cells

Scientists Discuss High-Throughput Sequencing Projects

 
Pink Ribbon
High-Throughput NGS to Identify Breast Cancer Targets

The Breast Cancer Atlas Project involves sequencing more than a million individual breast cancer cells to help researchers identify potential therapeutic targets.

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Plants
High-Throughput Sequencing Supports Australia Genome Center Growth

Implementing high-capacity NGS allowed the Deakin Genomics Centre to expand projects for species ancient and new, large and small.

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GLOBAL Clinical Study
Value of a Panomics-Based Drug Discovery Approach

A large clinical study that integrates sequencing with imaging, multiomic technologies, and big data uncovers novel therapeutic targets for chronic diseases.

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Recent advances in sequencing technologies have allowed for the development of 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
High-Throughput Library Prep Automation

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

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Multiplex Sequencing

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

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Large-Scale Sequencing Products

Single-lot shipments and other features empower clinical labs to reduce the frequency and cost of revalidating reagents and protocols.

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Bioinformatics Pipeline Setup

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

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LIMS for NGS

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

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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
Polygenic Risk Scores Could Become Useful Tools in the Physician's Toolbox

Researchers discuss large GWAS studies to identify disease-associated DNA risk loci and develop PRSs for clinical validation.

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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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Infinium Global Screening Array

A next-generation genotyping array for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research.

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Infinium XT

A comprehensive microarray solution for production-scale genotyping of up to 50,000 single or multi-species custom variants.

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Illumina Array LIMS

This state-of-the-art LIMS facilitates high-throughput microarray processing and sample tracking, using advanced automation and precise robotic control.

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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 in a learning health system.

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High-Throughput Genotyping

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

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SBS Technology

Illumina sequencing technology uses fluorescently labeled reversible terminators to detect bases as they’re incorporated into growing DNA strands.

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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.

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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.

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Shared Vision for the Power of Human WGS
Shared Vision for the Power of Human WGS

Genomics leaders share their perspective on the impact of high-throughput and population sequencing in clinical research.

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Chan Zuckerberg Biohub and the NovaSeq System
Chan Zuckerberg Biohub and the NovaSeq System

The Chan Zuckerberg Biohub uses the NovaSeq System to conduct innovative experiments in genomics.

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