Introduction to Next Generation Sequencing

Date:

 Tuesday 28 Friday 31 October 2014

Venue: 

European Bioinformatics Institute (EMBL-EBI) - Wellcome Genome Campus, Hinxton, Cambridge,  CB10 1SD, United Kingdom

Participation: 

Open application with selection

Contact: 

Frank O’Donnell

Registration fee: 

£495

Registration closed

Overview

This course will provide an introduction to technology, data analysis, tools and resources for next generation sequencing (NGS) data. The content is intended to provide a broad overview of the subject area, and to highlight key resources, approaches and methodologies. Topics will be delivered using a mixture of lectures, practical sessions and group discussions. Analysis work during the course will use small, example datasets and there will not be scope to analyse personal data.

 

Audience

This course is aimed at wet-lab biologists who are embarking upon research projects that will involve NGS and the analysis of the data generated.

Participants will require basic knowledge of the Unix command line, Bio-Linux 7 and the R statistical package. We recommend these free tutorials:

Please note, participants without basic knowledge of these resources will have difficulty in completing the practical sessions.

Syllabus, tools and resources

During this course you will learn about:

  • NGS platforms and NGS data files and formats
  • NGS bioinformatics workflow steps following sequence generation
  • Experimental NGS design and planning for your bioinformatics needs
  • NGS for genomics; assembly, alignment, QC and variant calling tools
  • NGS for transcriptomics; QC, mapping, visualisation tools
  • EMBL-EBI resources - Baseline Atlas, CRAM toolkit and ENA - used for further work, data management and sequence submissions

Outcomes

After this course you should be able to:

  • Discuss a variety of applications and workflow approaches for NGS technologies
  • Use a range of bioinformatics software and tools to undertake basic analysis of NGS data
  • Understand the advantages and limitations of NGS analyses
  • Submit, browse and access a range of NGS data available in public repositories using EBI resources

Programme

Time Topic Trainer
Day 1 - Tuesday 28  October 2014
12:00 - 13:00 Registration and Lunch  
13:00 - 13:30 Welcome to EMBL-EBI  Tom Hancocks
13:30 - 14:00 Introduction and networking activities  Tom Hancocks
14:00 - 15:00 Overview of NGS technologies  Tom Hancocks
15:00 - 15:30 Tea/Coffee  
15:30 - 17:30 Overview of NGS bioinformatics  Josh Randall
19:00 Dinner at Hinxton Hall (on campus)  
Day 2 - Wednesday 29 October 2014
09:00 - 10:30 Read assembly  Daniel Zerbino
10:30 - 11:00 Tea/coffee  
11:00 - 12:00 Read assembly  Daniel Zerbino
12:00 - 12:30 European Nucleotide Archive  Marc Rossello
12:30 - 13:30 Lunch  
13:30 - 15:00 Re-sequencing and variant calling  Josh Randall
15:00 - 15:30 Tea/Coffee  
15:30 - 18:00 Re-sequencing and variant calling  Josh Randall
19:00 Dinner at Hinxton Hall (on campus)  
Day 3 - Thursday 30 October 2014
09:00 - 09:30 RNA-Seq and Ensembl Genebuild  John Collins
09:30 - 10:30 Genebuild RNA-Seq analysis practical  Rishi Nag, Dan Murphy
10:30 - 11:00 Tea/Coffee  
11:00 - 12:30 RNA-Seq analysis  Simon Andrews
12:30 - 13:30 Lunch  
13:30 - 15:00 RNA-Seq analysis practical  Simon Andrews
15:00 - 15:30 Tea/Coffee  
15:30 - 17:00 RNA-Seq analysis practical  Simon Andrews
17:00 - 18:00 Array Express & Expression Atlas  Amy Tang
19:00 Dinner at Hinxton Hall (on campus)  
Day 4 - Friday 31 October 2014
09:00 - 10:00 ENA for your NGS workflow  Marc Rossello
10:00 - 10:30 Tea/coffee break  
10:30 - 11:30 1000 Genomes Project  Laura Clarke
11:30 - 12:30 NGS Special lecture  Elizabeth Murchison
12:30 - 13:00 Discussion and feedback  Tom Hancocks
13:00 Lunch and end of course  
14:15 Bus to Cambridge train station  

Course materials for download:

Course_Materials_Part_1.zip

Course_Materials_Part_2.zip