How to streamline bulk RNA-Seq analysis and increase productivity—point, click, and done

Join this scientific conversation where we discuss the start-to-finish bulk RNA-Seq analysis process, including what it is, why you do it, and considerations you need to make. As we progress through the conversation, we will demonstrate how to perform each analysis step using simple point-and-click actions that you can replicate in your own analysis.

Learn how to:

• Align sequence reads
• Perform quality control to determine data quality
• Quantify reads to an annotation model
• Identify and apply the best statistical method for your experiment
• Interpret differentially expressed gene sets

Speakers:

	Jennifer Mosher	Matteo Luberti, PhD
	Sr. Product Marketing Manager, Illumina	Sr Bioinformatics Applications Scientist, Illumina

M-GL-03090