Introduction to Bulk RNA-seq data analysis
17th, 24th Nov and 1st Dec
Online
Bioinformatics Training Facility, Craik-Marshall Building, Downing Site, University of Cambridge
Instructors
- Abigail Edwards - Bioinformatics Core, Cancer Research UK Cambridge Institute
- Adam Reid - Gurdon Institute, University of Cambridge
- Tom Smith - MRC Toxicology, University of Cambridge
- Ulrika Yuan - Department of Biochemistry, University of Cambridge
- Zac Scurlock - Department of Pathology, University of Cambridge
Outline
In this workshop, you will be learning how to analyse RNA-seq data. This will include read alignment, quality control, quantification against a reference, reading the count data into R, performing differential expression analysis, and gene set testing, with a focus on the DESeq2 analysis workflow. You will learn how to generate common plots for analysis and visualisation of gene expression data, such as boxplots and heatmaps.
This workshop is aimed at biologists interested in learning how to perform differential expression analysis of RNA-seq data.
Whilst we have run this course for several years, we are still improving and learning how to
teach it best.
Please bear with us if there are any technical hitches, and
be aware that timings for different sections laid out in the schedule below may
not be adhered to. There may be some necessity to make adjustments to the course
as we go.
Prerequisites
**Some basic experience of using a UNIX/LINUX command line is assumed**
**Some R knowledge is assumed and essential. Without it, you will struggle on this course.** If you are not familiar with the R statistical programming language we strongly encourage you to work through an introductory R course before attempting these materials. We recommend our Introduction to R course
Shared Google Document
This Google Document contains useful information and links.
Please use it to post any long form questions you have during the course.
The trainers will be monitoring the document and will answer questions as quickly as they can.
Introduce Yourself
There is another Google Doc Google Document.
Please write a couple sentences here to introduce yourself to the class, tell us a bit about your background and what you hope to get out of this course.
If you are a student or staff at the University of Cambridge, tell us which Department you are in.
Course etiquette
As this course is being taught online and there are a large number of participants, we will all need to follow a few simple rules to ensure things run as smoothly as possible:
-
Please mute your microphone
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To get help from a tutor, please click the “Raise Hand” button in Zoom:
This can be found by clicking on the ‘Participants’ button. A tutor will then contact you in the chat. If necessary, you and the tutor can be moved to a breakout room where you can discuss your issue in more detail.
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Please ask any general question by typing it into the Google Doc mentioned above
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During practicals, when you are done, please press the green “Yes” button:
This way we will know when we can move on.
Timetable
Day 1
Trainers: Abbi, Adam, Ulrika, Tom, Zac
9:30 - 9:45 - Welcome!
9:45 - 10:15 - Introduction to RNAseq Methods - Tom
10:15 - 11:00 Raw read file format and QC - Adam
11:00 - 13:30 Alignment and Quantification of Gene Expression with Salmon - Adam
13:30 - 14:30 Lunch
14:30 - 15:30 QC of alignment - Ulrika
15.30 - 17.30 Data Exploration in R (pdf) - Abbi
Day 2
Trainers: Abbi, Adam, Raquel, Tom
9:30 - 10:15 Introduction to RNAseq Analysis in R - Abbi
10:15 - 13:00 Statistical Analysis of Bulk RNAseq Data
- Part I: Statistics of RNA-seq analysis - Abbi
- Part II: Linear Models in R and DESeq2 (pdf) - Abbi
- Slides
- Find the worksheet in
Course_Materials/stats/models_in_r_worksheet.R
13:00 - 14:00 Lunch
14:00 - 17:30 - Differential Expression for RNA-seq (pdf) - Adam
Day 3
Trainers: Abbi, Adam, Ulrika, Raquel
9.30 - 9.45 - Recap of Day 1 and 2 - Abbi
9.45 - 12.30 Annotation and Visualisation of RNA-seq results - Ulrika
12.30 - 13.30 Lunch
13.30 - 16:30 Gene-set testing - Abbi
Data, software and materials
The lecture slides and other source materials, including R code and practical solutions, can be found in the course’s Github repository
The full data used in the course can be downloaded from dropbox.
Instructions to install software are available from the “Software installation instructions” page.
Extended materials
The Extended Materials contain extensions to some of the sessions and additional materials, including instruction on downloading and processing the raw data for this course, a link to an excellent R course, and where to get further help after the course.
Additional Resources
Acknowledgements
This course is based on the course RNAseq analysis in R prepared by Combine Australia and delivered on May 11/12th 2016 in Carlton. We are extremely grateful to the authors for making their materials available; Maria Doyle, Belinda Phipson, Matt Ritchie, Anna Trigos, Harriet Dashnow, Charity Law.
The materials have been rewritten/modified/corrected/updated by various contributors over the past 5 years including:
Abigail Edwards Ashley D Sawle Chandra Chilamakuri Dominique-Laurent Couturier Guillermo Parada González Hugo Tavares Jon Price Mark Dunning Mark Fernandes Oscar Rueda Sankari Nagarajan Stephane Ballereau Tom Smith Zeynep Kalender Atak
Apologies if we have missed anyone!