This course will introduce you to the basic data structures and genomic data analysis in Bioconductor. Specifically, we will focus on the basics of RNAseq analysis, including differential expression, annotation, and gene set analysis. We will also focus on loading data and metadata into data structures such as SummarizedExperiment. By the end of this course, you should be familiar with a basic RNAseq analysis workflow utilizing RNAseq count data.
Please note that this course requires the Intro to R course as a prerequisite, or the equivalent course. Please note that this course does not cover RNAseq workflows such as MultiQC and alignment.
Dates: Spring 2026: April 28, May 5, 12, 19, 26, June 2
Time: Tuesdays Noon - 1:30 pm PT
Time commitment: 6 weeks of 1.5 hour classes and 1-2 hours of practice outside class.
Audience: FH Research Staff wanting to use Bioconductor to analyze RNA-seq data
Prerequisites: Intro to R
Followed by: None
Explain and Utilize Bioconductor data structures such as SummarizedExperiment to integrate metadata and assay data in your analysis
Explore, QC, and clean a RNAseq dataset
Utilize Differential Expression analysis on an RNAseq dataset using Bioconductor Packages
Identify and Annotate Gene Sets for downstream analysis
Load data from RNAseq experiments into Bioconductor
This class is offered twice a year (currently fall and spring quarters). Check the schedule to see when it will next be offered.
Yes, you can access the course materials on your own any time.
You need to complete the live class to get a badge.
The class is open to members of the Cancer Consortium including Fred Hutch, the University of Washington, and Seattle Children’s Hospital.
You can, but we recommend you don’t mix R and Python at the same time, because it can be confusing to switch between the two.
You can sign up more than once, but be aware that there is tyspically a waitlist. We will prioritize students who have not taken the class. If there is room you are welcome to take it again.