• WHAT: Bulk RNA-Seq
  • WHEN: February 19th, 10am-12pm & 1-3pm
  • WHERE: Scaife Hall, Falk Library, Classroom 2
  • WHO: Ansuman Chattopahyay & Sri Chaparala
  • HOW: Register here


Workshop Objective:

This is a 4-hour workshop on the techniques, platforms, and methods used in analyzing bulk RNA-Seq data. The morning session (10am – 12pm) starts with a presentation from the Genomics Research Core on best practices in sample handling, followed by an overview of the basic steps involved in bulk RNA-Seq data analysis. The afternoon session (1pm – 3pm) focuses on hands-on practice using HSLS-licensed CLC Genomics Workbench software.

Participants will learn how to

  • access the CLCbio Genomics Server hosted on the HTC Cluster by Pitt CRC
  • import RNA-seq FASTQ reads from a GEO dataset
  • assess quality of RNA-seq data
  • align reads to a reference genome
  • estimate known gene and transcript expression
  • perform differential expression analysis
  • discover novel isoforms

Target Audience:

Experimental biologists seeking to analyze bulk RNA-Seq data generated through experiments or retrieved from a repository such as GEO. The software covered in the workshop operates through a user-friendly, point-and-click graphical user Interface, so neither programming experience nor familiarity with command line interface is required.

Workshop Requirements:

Workshop Guide:

Suggested Reading:

Attribution:

Please include the following statement in the acknowledgments section for all publications, posters, and presentations: Data analysis was performed using {name of software} software licensed through the Molecular Biology Information Service of the Health Sciences Library System, University of Pittsburgh.

HSLS Winter/Spring MolBio Info Service Training Workshops schedule

Contact the HSLS Molecular Biology Information Service with any questions.