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Next Generation Sequencing

21–28 March 2025, Wellcome Genome Campus, UK

Wellcome Connecting Science Course Run Website
Course Informatics Guide

Hands-on lab and informatics training for long and short-read sequencing

Summary

Next-generation sequencing (NGS) has become the premier tool in genetic and genomic analysis. This hands-on laboratory and informatics course is directed at scientists who will be generating and interpreting sequence information in their research and wish to improve their understanding of various sequencing platforms, techniques, and their applications.

Participants will be able to make informed decisions about appropriate techniques to apply in a variety of research contexts. Training will cover applications for target enrichment, bacterial sequencing, cancer genomic analysis, human variation analysis, and RNA-Seq.

What will this course cover?

The programme will include theoretical and practical information on NGS systems currently available and those on the near horizon. Technologies will be chosen from short- and long-read sequencing platforms including:

  • PacBio
  • Illumina Miseq/HiSeq/Novaseq
  • Oxford Nanopore MinION

All the basic techniques of post-sequencing analysis will also be covered in hands-on genomics data analysis sessions including QC, sequence alignment, and variant calling.

Target Audience

Applications are open to clinical, industry, research professionals, and university students who are either engaged in next-generation sequencing or are aiming to implement it into their future workflows.

This course is not meant to replace the manufacturers’ training normally supplied with new instruments, nor is it intended to be a training course for those solely interested in NGS data analysis (please refer to our website for dedicated bioinformatics courses).

Learning outcomes

What will you achieve

Upon completion of the course, participants should be able to:

  • prepare high quality sample libraries for use on next generation sequencing platforms
  • set up sequencing runs for the various platforms utilised during this course
  • critically assess a sequencing run and distinguish between good and poor-quality data
  • describe the advantages and disadvantages of different sequencing technologies in order to select technologies appropriate to specific needs
  • process NGS data and use computational tools for sequence alignment and variant-calling

Programme

The programme will include lectures, seminars, practical sessions, and social events covering the following topics:

Library Prep

  • Preparing high-quality libraries from samples

Sequencing

  • Overview: Motivation and fundamental concepts
  • Detailed description of prominent sequencing technologies: current and emerging platforms
  • preparing chips for sequencing and performing sequencing runs on various platforms

Data analysis

  • Data QC: How to determine if a sequencing run has performed well
  • Alignment to a reference sequence and variant-calling of NGS data

The course will also include seminars by invited speakers, who will highlight their ground-breaking work in the applications of next-generation sequencing.

Course Instructors

Wellcome Connecting Science Team


Citing and Re-using Course Material

To cite this course head over to the course homepage for instructions: Next Generation Sequencing Bioinformatics Homepage

The course data are free to reuse and adapt with appropriate attribution. All course data in these repositories are licensed under the Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). Creative Commons Licence

Interested in attending a course?

Take a look what courses are coming up at Wellcome Connecting Science Courses & Conference Website.


For more information or queries, feel free to contact us via the Wellcome Connecting Science website.


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