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Thu 9 Jun - Fri 10 Jun 2016
14:00, ...

Venue: Bioinformatics Training Room, Craik-Marshall Building

Provided by: Bioinformatics


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Thu 23 Jan 2025


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Using the Ensembl Genome Browser
BeginnersPrerequisites

Thu 9 Jun - Fri 10 Jun 2016

Description

The Ensembl Project provides a comprehensive and integrated source of annotation of, mainly vertebrate, genome sequences. This workshop offers a comprehensive practical introduction to the use of the Ensembl genome browser as well as essential background information.

This course will focus on the vertebrate genomes in Ensembl, however much of what will be covered is also applicable to the non-vertebrates (plants, bacteria, fungi, metazoa and protists) in Ensembl Genomes.

There may be some tools and topics that do not apply to non-vertebrates; if you have any questions about this, please email the Ensembl Outreach Project Leader, Emily Perry.

Please note that if you are not eligible for a University of Cambridge Raven account you will need to Book or register Interest by linking here.

Target audience
  • Graduate students, Postdocs and Staff members from the University of Cambridge, Affiliated Institutions and other external Institutions or individuals
  • Further details regarding eligibility criteria are available here
  • Further details regarding the charging policy are available here
Prerequisites
  • Basic computing skills
  • Graduate level in Life Sciences
  • Knowledge of basic genetics and basic bioinformatics terminology is very helpful for this course
Sessions

Number of sessions: 2

# Date Time Venue Trainer
1 Thu 9 Jun 2016   14:00 - 17:30 14:00 - 17:30 Bioinformatics Training Room, Craik-Marshall Building Emily Perry
2 Fri 10 Jun 2016   09:30 - 13:00 09:30 - 13:00 Bioinformatics Training Room, Craik-Marshall Building Emily Perry
Topics covered
  • Introduction to Ensembl: origin, goals and organization of the Ensembl project
  • Worked example: guided tour of the most important pages of the Ensembl website
  • Data mining with BioMart: retrieving datasets using the data mining tool BioMart
  • Comparative genomics and proteomics: orthologues, protein families, whole genome alignments and syntenic regions
  • Variation: SNPs and other polymorphisms, haplotypes, linkage disquilibrium, structual variants like CNVs
Aims

To enable participants to access genomes with confidence

Format

Presentations, demonstrations and practicals

Notes

Participants are encouraged to bring problems/questions about their research to try to tackle these during the workshop using Ensembl

Duration

1

Frequency

A number of times per year

Themes

Booking / availability