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Meet Your New Lab Partner

24085 views | 8 years ago

Introducing the iSeq 100, the latest advancement in the world of next-generation sequencing (NGS) from Illumina. The iSeq 100 instrument leverages Illumina technological advances in its smallest and...

Sequencing amplified: AmpliSeq™ for Illumina®

19968 views | 8 years ago

The latest addition to the Illumina library prep portfolio, the AmpliSeq for Illumina solution provides a simple, fast, and robust amplicon sequencing option to achieve high-confidence data from even...

Custom Content Creation: AmpliSeqTM for Illumina®

3229 views | 8 years ago

Create custom content on the AmpliSeq for Illumina solution—the new workflow for your targeted next-generation sequencing (NGS) studies. Learn how to design custom panels with our DesignStudio software,...

Data Analysis with Local Run Manager: AmpliSeqTM for Illumina®

2743 views | 8 years ago

Accelerate your research with the AmpliSeq for Illumina solution—the new workflow for your targeted next-generation sequencing (NGS) studies. Learn how to perform on-premises amplicon analysis using...

Data Analysis with BaseSpace® Sequence Hub: AmpliSeqTM for Illumina®

5538 views | 8 years ago

Simplify data analysis on the AmpliSeq for Illumina solution—the new workflow for your targeted next-generation sequencing (NGS) studies. Learn how to analyze, store, and share your data using BaseSpace...

Tertiary Analysis with BaseSpace® Variant Interpreter: AmpliSeqTM for Illumina®

2120 views | 8 years ago

Accelerate your research with the AmpliSeq for Illumina solution—the new workflow for your targeted next-generation sequencing (NGS) studies. Quickly identify, annotate, and classify disease-relevant...

Selective Advances in Cattle Breeding | Adventures in Genomics

10637 views | 8 years ago

The world population is continuously growing. As the second largest producer and largest exporter of beef in the world, Brazil has an important role in feeding such a population. Jacques and Irene from...

Sophia’s iHope Story: Diagnosing a Rare De Novo Mutation

6142 views | 8 years ago

Sophia and her family spent years in search of a diagnosis for her condition. Finally, a de novo mutation was discovered through a clinical whole genome sequencing (cWGS) test she received from the...