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Illumina CEO: Chasing Challenges & Transforming Global Health

238 views | 2 days ago

A career chasing big challenges. An unexpected calling to shape global health. Our CEO shares the real story behind Illumina's strategy, what sets us apart, and the journey that brought him here. In...

Experience with the Illumina Spatial Technology (StrataMap™ Spatial Solution)

107 views | 4 days ago

Dr. Ioannis Vlachos of Harvard Medical School describes how the high sensitivity, broad coverage, and cellular resolution of Illumina StrataMap Spatial Solution has enabled spatial analysis of challenging...

Single-nucleus RNA-sequencing uncovers new mechanisms for cachexia in cancer

130 views | 1 week ago

In this video, you will see why muscle loss in pancreatic cancer is far more complex than previously understood. Using PIPseq single-nucleus RNA sequencing from Illumina, researchers mapped transcriptional...

ESHG insights: Emma Baple on bringing whole-genome sequencing into clinical research

101 views | 1 week ago

At the European Society Human Genetics 2026 conference in Gothenburg, Sweden, more than 6000 global leaders across research, healthcare, and industry came together to discuss the latest advances in...

Empowering Research, Enabling Discovery - Human Technopole National Facility for Genomics

76 views | 1 week ago

Behind every breakthrough in genomics stands a team committed to enabling others to succeed. In this video, Clelia Peano, Francesca Giannese, and Luca Rotta from Human Technopole National Facility for...

DRAGEN™ v4.5 | TruPath™ Genome: Phasing That Outperforms Long Reads

63 views | 1 week ago

Discover how Illumina TruPath Genome paired with DRAGEN v4.5 delivers phased variant calls that outperform long-read sequencing — phasing up to 98% of genes (HMW input) with phase blocks spanning millions...

DRAGEN™ v4.5 | Somatic Machine Learning Eliminating the FFPE Noise Floor with 93% Fewer False Positi

49 views | 1 week ago

Eliminate FFPE noise with machine learning (ML). DRAGEN v4.5 introduces ML-driven somatic variant calling that reduces SNV false positives by 93% in FFPE benchmarks, with 5–20% lower FP+FN overall and...

DRAGEN™ v4.5 | STAR Aligner for Single-Cell RNA-Seq — No FPGA Required

26 views | 1 week ago

No DRAGEN hardware? No problem. DRAGEN v4.5 introduces the STAR Aligner as a software-only alternative to the DRAGEN mapper for single-cell RNA-seq analysis — making DRAGEN accessible to any lab without...