Thursday, March 3 @ 1:00 P.M. EST

Presented by: Illumina and the BRCF Advanced Genomics Core

RNA sequencing (RNA-seq) is a highly sensitive and accurate method for measuring expression across the transcriptome and is one of the most cited NGS methods. Bulk RNA-Seq experiments provide insight into overall sample gene expression, while single-cell RNA-Seq can provide information on individual cell types or populations. Overall, RNA-Seq can enable the detection of transcript isoforms, gene fusions, single nucleotide variants, and other features without the limitation of prior knowledge about the transcriptome.

The Illumina team invites you to join our webinar for an introduction to RNA-Seq, with insight into library preparation, analysis solutions, and potential applications.

Register Here:
https://eventregistration.illumina.com/event/979435e2-6e84-4522-8c87-dc59501b377a/summary 

Presenter:

Kayla Zochowski, Ph.D., Sr Sales Specialist, Illumina, Inc.