Genome Sequencing Bioinformatics Africa 2023 Course

International
Posted 11 months ago
Sequencing has become an essential tool in genetic and genomic analysis. It is increasingly important for experimental scientists to gain the bioinformatics skills required to analyse the large volumes of data produced by sequencers. This course aims to equip participants with the essential informatics skills required to begin analysing data and apply some of the most commonly used tools and resources for sequence data analysis.

The programme covers prominent sequencing technologies, algorithmic theory, and principles of bioinformatics, with a strong focus on practical computational sessions using sequence analysis techniques and tools applicable to any species or genome size. A variety of applications will be covered from post-sequencing analysis, quality control, reference  alignment, and variant calling.

The course will cover the following topics:

• Intro to Unix/Linux & running workflows
• Introduction to Sequencing Technologies
• sequencing data pre-processing and QC
• Alignment to reference sequences
• Variant calling and annotation

Intended Audience:

Applicants should be postdoctoral scientists, senior PhD students, junior faculty members or clinicians/healthcare professionals actively engaged in or soon to commence research involving next generation sequencing data analysis.

Priority will be given to applicants who 1) currently or will soon have NGS experimental data to analyse 2) will utilise the bioinformatics techniques taught in at least two of the modules/topic areas listed in the programme outline in their experiments 3) have a clear plan/opportunity to disseminate the knowledge amongst their peers. We encourage applicants to highlight these areas in their application.

Learning Objectives:

After this workshop participants should be able to:
  • Use the unix command-line as a tool for data analysis
  • Describe the different NGS data file formats available
  • Perform QC assessment of high throughput sequencing data
  • Explain the algorithmic concepts behind read alignment, variant calling and structural variant detection
  • Perform read alignment, variant calling and structural variation detection using standard tools
If you would like to apply to be a participant of the course in 2023, please follow this link.

Applications are due on: Thursday, 29 June 2023 at 11;59 pm CAT.
No late applications will be accepted.

(For more background on the course, refer to the website:  https://www.h3abionet.org/categories/event/course/genome-sequencing-bioinformatics-africa-gsb-africa-2023 or the flyer on the right)

Click here to apply now!

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