Date:Tuesday 11 - Wednesday 12 June 2019
Venue:University of Belgrade, Institute of Molecular Genetics and Genetic Engineering - Vojvode Stepe 444a, 11010, Belgrade, Serbia
Application opens:Saturday 04 May 2019
Application deadline:Friday 10 May 2019
Participation:Open application with selection
Registration fee:5000 RSD / 45 EUR
The Ensembl project provides a comprehensive and integrated source of annotation of mainly vertebrate genome sequences. The 1000 Genomes Project created the largest public catalogue of human variation and genotype data. Its goal was to find most genetic variants with frequencies of at least 1% in the populations studied. The International Genome Sample Resource (IGSR) provides ongoing support for the 1000 Genomes Project data.
This two-day workshop offers participants the possibility of gaining hands-on experience in the use of Ensembl and the interlinked IGSR, but also provides them with the necessary background information. Participants will learn how to use a variety of tools for analysing variation data, including the Variant Effect Predictor (VEP).
The workshop is primarily targeted at wetlab researchers, and we customise the course to include total beginners of Ensembl/IGSR up through frequent users.
Feedback from previous courses: "There are probably quite few people out there who all assume that Ensembl today is the same as it was years ago. It is not. With many new features and datasets incorporated/interlinked, it offers data exploration like never before. This course was a very useful update on what Ensembl has become" Browser workshop, CRUK, April 2016
"Very useful workshop, certainly one of the most informative and useful I have attended. Delivered by someone who was extremely familiar with the website and its capabilities, not someone who had used it a couple of times and proclaimed themselves to be an expert." Browser workshop, Cardiff, March 2014
If you think you'd like to host a similar course at your institute, you can find out more on the Ensembl workshops page.
wet-lab researchers and bioinformaticians
Participants should be able to:
view genomic regions and manipulate the view to add features they are interested in
explore information about genes and their sequences, and gene data in bulk using BioMart
analyse genomic variants and associated phenotypes and their own variation data using the VEP
view homologous genes and genomic regions, functional elements involved in gene regulation and their activity in different cell types
find and access 1000 Genomes Project data, as well as more recently included data sets, by using the IGSR resource
use a variety of tools for analysing variation data, and tools specifically developed for use with 1000 Genomes Project data.
Introduction to Ensembl. Genes and transcripts. Viewing genes and locations in the browser. Comparative Genomics. Gene regulation.
Variation data in Ensembl and the Variant Effect Predictor (VEP). The 1000 Genomes project and International Genome Sample Resource (IGSR). Upload of custom data to Ensembl and data export with BioMart.