A platform that enables the visualisation of individual genes for evidence of reannotation.
Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders
David Zhang, Sebastian Guelfi, Sonia Garcia-Ruiz, Beatrice Costa, Regina H. Reynolds, Karishma D'sa, Wenfei Liu, Thomas Courtin, Amy Peterson, Andrew E. Jaffe, John Hardy, Juan A. Botía, Leonardo Collado-Torres, and Mina Ryten
SCIENCE ADVANCES, 10 Jun 2020, Vol 6, Issue 24, DOI: 10.1126/sciadv.aay8299
This repository contains the User Interface (UI) code for the vizER platform.
Additionally, on the Wiki section, there is available a tutorial that fully explain the configuration needed to be able to install and expose vizER in a Linux web server environment.
vizER platform is fully working and can be reached following this link.
- Sonia García-Ruiz - vizER UI developer.
- Get in touch with Sonia García at s.ruiz@ucl.ac.uk.
- David Zhang - vizER backend developer and first author of 'Incomplete annotation of OMIM genes is likely to be limiting the diagnostic yield of genetic testing, particularly for neurogenetic disorders'.
- Get in touch with David Zhang at david.zhang12@ucl.ac.uk.
- All RytenLab members
- University College of London
- University of Murcia