Bring Your Own Data: R-coding for analysing RNA-seq data

Important

For in person courses you need to bring your own laptop and have R and Rstudio installed.

Please refer to the tab 'additional important information' for requirements.

Target Audience

Basic understanding of R and R-studio is required.  If you do not have this yet, consider to take the course 鈥淚ntroduction to R for Life Sciences鈥  first. In addition, the course will be easier to follow with some knowledge of the R package ggplot2. If you do not have this yet, consider taking the course Bring your Own Data: create figures in R using ggplot2.

Course description

During this BYOD course you learn processing RNA-seq (and similar types of) data by applying lessons to your own data. If you do not have your own data, you can use data from colleagues or download a data set from a paper or a database like the EBI expression atlas (). Your data should be a count table that you can load into R, so no raw reads!

This course is aimed at PhD candidates proficient in R programming but with little or no experience in analysing RNA-seq data. The course is also well-suited for PhD candidates who have analysed RNA-seq data before, but seek a deeper understanding of the many possible analyses.

One week of full focus, and we could all present some results with our data already!

Entrance fee: This course is free for GSLS PhD candidates.

Unfortunately we don鈥檛 offer this course for participants not part of the GSLS. Our courses tend to be fully booked by GSLS PhD candidates

Location: Utrecht Science Park

Registration for this course opens 2 months before the course starts. You can register via our course portal (see registration link below). After opening, the portal shows how many spots are still available. You can subscribe to the interest list when a course is fully booked or not yet open for registration. When a new edition opens for registration you will receive an e-mail.