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Xing Cancer Care: Simplifying NGS Data Analysis with BaseSpace Sequence Hub and DRAGEN

365 views | 9 months ago

Developing and setting up a new NGS analysis pipeline can be a time and money-consuming venture. Lynn Fink, Lab Director at Xing Cancer Care in Brisbane Australia shares how she uses Illumina’s BaseSpace...

Impact of Genetic Sequencing for Rare Disease Diagnosis

138975 views | 9 months ago

In the search for a rare disease diagnosis, whole genome sequencing has the opportunity to provide answers earlier and can make a difference in care. Interested in learning about how a panomics-based...

GeneDx: Enabling Operational Growth with DRAGEN

497 views | 9 months ago

Kyle Retterer, Chief Innovation Officer at GeneDx, details how his company seamlessly integrated the DRAGEN Server into its existing on-premises solution to lower costs and reduce turnaround times,...

Diagnosing Suboptimal Clustering in Patterned Flow Cells

76 views | 9 months ago

Although over clustering is not possible on patterned flow cell, loading a library with a suboptimal concentration negatively impacts run data. In this video, we will discuss preventing and diagnosing...

Optimal Cluster Density Best Practices

39 views | 9 months ago

In this video, we will discuss optimal cluster density and how over and under-clustering can affect your sequencing data. We will then examine common clustering issues and ways to prevent them. More...

Diagnosing Suboptimal Clustering in Nonpatterned Flow Cells

54 views | 9 months ago

In this video, we will highlight which run metrics and thumbnail images to monitor during a run to diagnose over clustering of a nonpatterned flow cell. More resources: The Cluster Optimization Overview...

Removing Uncertainty on World Cancer Day

259 views | 10 months ago

On this World Cancer Day, learn how next-generation sequencing can remove the uncertainty of cancer, so you can focus on your future: http://www.illumina.com/wcd Subscribe to the Illumina video channel...

TruSight Software Suite—Supporting Variant Analysis in Rare Disease

788 views | 10 months ago

Next-generation sequencing (NGS) is becoming commonplace when seeking a diagnosis for rare genetic disease. This can create a bottleneck when analyzing and interpreting the billions of base pairs and...