Cold Spring Harbor Laboratory is hosting a course, “Tutorials in Genomics & Bioinformatics: RNA-Seq Analysis,” an intensive two-day introductory course to genomics and bioinformatics, from April 28-30, 2024. The course is broken into modules that are each designed to give a broad overview of a given topic; a brief lecture describing the theory, methods and tools is followed by a set of worked examples that students complete. Students have opportunities to ask the instructors about tasks or problems they have encountered in their research. Students will be afforded hands-on experience by re-analyzing a published bulk RNA-Sequencing data, featuring resources and examples that primarily come from mammalian species, but are applicable to any species with a reference genome assembly.
Topics include:
Designing RNA-Seq Studies
Best practices in the design of bulk RNA-Seq studies.
Caveats in analysis workflows
Analysis of High-Throughput Sequence Data Using Galaxy
Importing FASTQ files
Importing reference genomes and annotation
Read quality control and diagnostics
Read trimming
Read mapping and read count estimation
Introduction to R
Basic Syntax
Data Structures
Reading input and writing input
Plotting basics
Analysis of RNA-Seq Read Counts using R/DESeq2
Diagnostic analyses
Normalization
Model fitting
Testing for differentially expressed genes
Data visualization (heatmaps, volcano plots)
Genome Browser Resources
Genome annotation
Functional genome data
Bulk Genome analysis
Gene Set Enrichment and Pathway Analysis
Gene set enrichment analysis using Gene Ontology and pathway annotations
Although the course is open to all on a first-come, first-served basis, it is most beneficial for bench scientists transitioning into projects that require intensive analysis or integration of large data sets. It is not appropriate for those with significant programming or data analysis experience.
The class is currently full, but prospective students can register for the waitlist. For more information see the course website.