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.