Are you a life science professional? Please take 10-15 minutes of your time to fill this anonymous survey* aiming to understand and improve the usage of existing infrastructure, resources and protocols for human genome variation annotation and curation.
Goal and outcome of the survey
The survey, launched on behalf of the ELIXIR team and the Implementation study on annotating and curating human genomic variants, aims to understand and improve the usage of existing infrastructure, resources and protocols for human genome variation annotation and curation. The focus is on processes that can be automated to support interpretation of high-throughput genome sequencing results for research as well as for clinical use.
The outcome of the survey will be a report that describes the current status within ELIXIR member states, identified requirements and potential solutions. The report will be part of the ELIXIR Human Genomics and Translational Data Services strategy and roadmap, and will be published on the ELIXIR website in late 2019.
What is ELIXIR
ELIXIR is a non-profit, intergovernmental organisation that brings together life science resources from across Europe. These resources include databases, software tools, training materials, cloud storage and supercomputers. The goal of ELIXIR is to coordinate these resources so that they form a single infrastructure. This infrastructure makes it easier for scientists to find and share data, exchange expertise, and agree on best practices. Ultimately, it will help them gain new insights into how living organisms work.
The survey is run by the following ELIXIR nodes and partners:
- CSC - IT Center for Science Ltd., Finland
- National Institute for Health and Welfare (THL), Finland
- Mitochondrial Bioinformatics Unit - University of Bari, Italy
- SIB Swiss Institute of Bioinformatics, Switzerland
- The European Bioinformatics Institute (EMBL-EBI), UK
- Imperial College London, UK