Description

PLEASE NOTE! This is a 5-day course. The first part (lectures and practicals) takes place 13-16 March. The second part (bring your own data session) takes place 27 March.

This workshop will introduce the best practice bioinformatics methods for analyzing single cell RNA-seq data via a series of lectures and computer practicals (using R or Python according to each student’s preference). The total course duration is 5 days, which includes 4 days of lectures and exercises followed by a "Bring Your Own Data" (BYOD) day where you get to practice your skills on a dataset of your choosing. Please note that the BYOD section will take place two weeks after the lectures.

Topics covered will include:
- Overview of the current scRNAseq technologies
- Basic overview of pipelines for processing raw reads into expression values
- Quality control and normalization
- Dimensionality reduction techniques
- Data integration and batch correction
- Differential gene expression
- Clustering techniques
- Cell type prediction
- Trajectory inference analysis
- Comparison of Seurat, Bioconductor and Scanpy toolkits

This online training event has no fee for academic participants. However, if you accept a position at the workshop and do not participate (no-show) you will be invoiced 3000 SEK. For non-academic participants, the course fee (and no-show fee) is 12000 SEK. Please note that NBIS cannot invoice individuals.

Event Details

Dates
13 - 27 April 2026
Application deadline
March 13, 2026 23:59
Contact

edu.sc@nbis.se

City
Online
Country
Sweden
Language
English
Cost
Free to all
Timezone
Stockholm

Content Providers

Learning Outcomes

Upon completion of this course, you will be able to run analysis on your own data, select appropriate analysis methods and interpret the results.

Prerequisites & Technical Requirements

Prerequisites

The following is a list of skills required for being able to follow the course and complete the exercises:

  • You are familiar with basic UNIX command line (bash)
  • You are familiar with R and/or Python
  • You understand the basics of NGS technologies
  • You are familiar with analyses of bulk RNA-sequencing data

The course accommodates a maximum of 25 participants. If we receive more applications, participants will be selected based on selection criteria including (but not limited to) correct entry requirements, motivation to attend the course, as well as gender and geographical balance. Priority is given to PhD candidates followed by other researchers. International applicants are accepted based on availability of seats.


Technical requirements

You will need to have full access to your computer (admin permissions). Instructions on installation will be sent by email to accepted participants.

Topics & Tags

Keywords
scRNA seqsingle cellRNAseqLife sciencesNGSbioinformaticsdata analysissequencing

Affiliations & Networks

Associated nodes
SciLifeLab
Target audience
researchersPhD students (prioritized), postdocs, researchers and other employees at all Swedish universitiesPhD studentspostdocsresearch engineersclinicianscore facility staffgroup leadersSciLifeLab Units

Activity log