Bioinformatics Workshop Series - Session 3: Upload bulk RNAseq data tables into RStudio and setup a DESeq2 analysis
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Bioinformatics Workshop Series - Session 3: Upload bulk RNAseq data tables into RStudio and setup a DESeq2 analysis In-Person
Registration Required
Workshop Series: Introduction to bulk RNA-seq analysis - from counts to functional analysis
Summary:
The Bioinformatics Support Hub has designed this hands-on teaching series for researchers interested in learning the basics steps for re-analysis of publicly available bulk-RNAseq data. Over the next two months, you can learn basic concepts concerning genomic data annotation and vocabulary, where to find bulk RNAseq data to re-analyze, how to perform differential gene analysis in RStudio and with point-click proprietary software, how to visualize your results, how to find transcription factors that may be regulating differentially expressed genes, and finally different approaches to perform gene pathway analysis. *Registrations for October sessions will open at the end of September.
Session 3. Upload bulk RNAseq data tables into RStudio and setup a DESeq2 analysis
Sequencing data is increasingly available in public repositories making it easier for reanalysis. Join us for the first part on how to run a differential gene expression analysis with *DESeq2.
In this session you will learn how to import tables containing the raw counts and metadata of a publicly available bulk-RNA seq dataset and setup a differential gene expression analysis using the R package DESeq2.
This workshop is designed for: biomedical researchers with none to minimal knowledge of command language or R programming.
You will learn how to:
- Use R packages *readr* to import data tables into RStudio
- Use basic R functions such as *view()* and *str()* to visualize and inspect data
- Import R package *DESeq2* into RStudio
- Assemble a DESeq2 data frame and design a differential gene expression analysis
- Run the function *DESeq()* and brief introduction to the function *results()*
If you are interested in understanding how to extract DESeq2 results when you have more than 2 groups to compare, consider attending session 4 of this series.
Details:
Target audience: These classes are meant to novices in bulk RNAseq analysis, with none to minimal knowledge in R programming.
Seating – in person classes are limited to 16 places.
Registrations - open to all interested. However, seating will be on “first come, first served” basis.
Recording – we will record the sessions so you can follow asynchronously.
Series Program:
Date |
Session |
Mode |
Presenter |
9/14/23 |
Session 1 - Intro to annotation of gene expression data |
In-person |
Rolando Milian |
9/21/23 |
Session 2 - Find, Download and Transform public bulk RNA seq data to analyze with DESeq2 in RStudio |
In-person |
Sofia Fertuzinhos |
9/28/23 |
Session 3 - Upload bulk RNAseq data tables into RStudio and setup a DESeq2 analysis |
In-person |
Sofia Fertuzinhos |
10/5/23 |
Session 4 - Manipulate DESeq2’s results() and plot functions |
In-person |
Sofia Fertuzinhos |
10/12/23 |
Session 5 – DEMO - Analyzing and Visualizing RNAseq public dataset using Qlucore Omics Explorer |
Online |
Yana Stackpole - Qlucore |
10/19/23 |
Session 6 – DEMO - Transcription factors analysis with TRANSFAC |
Online |
Volker – Transfac |
10/24/23 |
Session 7 - Functional analysis of omics data: Overrepresentation Analysis ORA |
In-person |
Rolando Milian |
10/26/23 |
Session 8 - Gene Set Enrichment Analysis GSEA |
In-person |
Rolando Milian |
- Date:
- Thursday, September 28, 2023
- Time:
- 10:00am - 12:00pm
- Time Zone:
- Eastern Time - US & Canada (change)
- Location:
- SHM L 111, Cushing/Whitney Medical Library, 333 Cedar Street
- Campus:
- Medical School
- Categories:
- Bioinformatics