DRAGEN secondary analysis

Accurate, comprehensive, efficient analysis

A suite of bioinformatics pipelines to process NGS data and maximize genomic discovery

Advances using DRAGEN secondary analysis

From genetic diseases to oncology to pharmacogenomics and more, DRAGEN secondary analysis can help labs in any field scale up NGS operations and make game-changing genomic analysis a reality.

How the UK is setting new standards for genomic research and better health care

DRAGEN secondary analysis helps UK Biobank identify ~1.5 billion variants from a half-million genomes.

Can genomics stop the world’s leading cause of death?

DRAGEN secondary analysis helps Cardio-CARE cut their data-processing time, reduce their data storage footprint by 80%, and rapidly analyze WGS data for a study with 9000+ participants.

A starring role for pharmacogenomics: “star allele” calling for 20 critical PGx genes

The DRAGEN PGx pipeline enables genotyping of 20 genes related to drug metabolism to support new drug development.

Featured resources

The quest for accuracy gains in the dark regions of the genomes: Presenting the DRAGEN multigenome mapper and pangenome reference updates in version 4.3

The evolution of the multigenome mapping methodology using pangenome references, showing significant accuracy improvements.

DRAGEN somatic indel calling wins PrecisionFDA NCTR challenge with highest precision and overall accuracy

Discover how DRAGEN somatic indel methods enabled high accuracy variant calling in the NCTR indel calling from Oncopanel Sequencing Data Challenge.

Overcoming the challenges in PMS2 high-homology regions for improved detection of pathogenic variants associated with Lynch syndrome

Discover how multi-region joint detection (MRJD) addresses the challenge of de novo germline variant calling in difficult to map regions of the genome.

DRAGEN secondary analysis

Meet Illumina DRAGEN

Key features and benefits

Accurate results

Comprehensive solution

Efficient analysis

Cost efficiency

Multiplatform accessibility

Streamlined integration

Key analysis apps and pipelines

Advances using DRAGEN secondary analysis

How the UK is setting new standards for genomic research and better health care

Can genomics stop the world’s leading cause of death?

A starring role for pharmacogenomics: “star allele” calling for 20 critical PGx genes

Featured resources

The quest for accuracy gains in the dark regions of the genomes: Presenting the DRAGEN multigenome mapper and pangenome reference updates in version 4.3

DRAGEN somatic indel calling wins PrecisionFDA NCTR challenge with highest precision and overall accuracy

Overcoming the challenges in PMS2 high-homology regions for improved detection of pathogenic variants associated with Lynch syndrome

Learn more or get in touch

For every lab, everywhere

Illumina Single Cell 3' RNA Prep

NGS Workflow Finder

DRAGEN secondary analysis v4.4 now available

Illumina Proactive Instrument Performance Service

Do more, faster than ever

Next-generation sequencing for beginners

Next-generation sequencing for beginners

Next-generation sequencing for beginners

Next-generation sequencing for beginners

Next-generation sequencing for beginners

Next-generation sequencing for beginners

Next-generation sequencing for beginners

Celebrate DNA Day with Your Students

Celebrate DNA Day with Your Students

Celebrate DNA Day with Your Students

Celebrate DNA Day with Your Students

Celebrate DNA Day with Your Students

Celebrate DNA Day with Your Students

Celebrate DNA Day with Your Students

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

For every lab, everywhere

DRAGEN secondary analysis

Meet Illumina DRAGEN

Key features and benefits

Accurate results

Comprehensive solution

Efficient analysis

Cost efficiency

Multiplatform accessibility

Streamlined integration

Deployment options

Key analysis apps and pipelines

Comprehensive coverage with leading edge innovations

Advances using DRAGEN secondary analysis

How the UK is setting new standards for genomic research and better health care

Can genomics stop the world’s leading cause of death?

A starring role for pharmacogenomics: “star allele” calling for 20 critical PGx genes

Featured resources