RNA-seq can reveal invaluable gene expression details and uncover the mysteries of the transcriptome. However, the path to achieving meaningful RNA-seq data is often not linear. You can encounter multiple setbacks – from long-winded workflows and low-input RNA to abundant rRNA and reduced RNA-seq sensitivity. When you’ve finally generated your precious RNA-seq data, figuring out how to make sense of it is yet another headache. 

We can help you overcome these obstacles and unlock the potential of RNA-seq for your research. Join our webinar, where we’ll guide you through the complexities of RNA-seq based on our many years of experience. Discover how to achieve and analyze high-quality and -quantity unique RNA reads faster.

We’ll discuss key areas of workflow optimization, including:

  • rRNA removal 
  • Library normalization
  • RNA data analysis, quantification and biological interpretation

Following the webinar, participate in the interactive Q&A session, where our RNA-seq expert will answer all your questions.

About the speaker
Samuel Rulli, PhD, Director, Global Product Management, RNA-seq profiling, NGS assay technologies
Dr. Samuel Rulli received his PhD in Molecular and Cellular Biology from Tulane University in 2002,studying the gastric proton pump. After his postdoctoral training at Johns Hopkins University and the National Cancer Institute, he joined QIAGEN in 2009. As the Associate Director of Global Product Management for NGS technologies, Samuel has been instrumental in developing gene expression analysis solutions for qPCR and NGS.
Date of recording:Tuesday, October 10, 2023
Duration:60 minutes
Academic Basic Research
Gene Expression/Regulation
Next Generation Sequencing