12/12/2023 0 Comments Wg sequencesMapping experimental and aggregated datasets onto genome sequences provides a powerful unifying model for data–driven analysis across data types, single cells, cell lines, tissues, genomes, and species. Immense research funding and countless work hours are invested in generating genomic datasets, encompassing both large–scale consortia initiatives and smaller–scale research projects, spanning across the past, present, and future. Please read on for more information on the background of this Working Group. More information and relevant links can be found in the working document of the initiative. Prior to the session, attendees have the opportunity to provide input to the group’s Case Statement - defining the group’s charter, value proposition, and engagement with other initiatives in the area. The initiative has been pre-selected as a demonstrator WG to take part in the Horizon Europe-funded RDA TIGER project, which will provide various support services to the WG throughout its lifespan. The work will continue as an open collaboration in a new Working Group (WG) in the Research Data Alliance (RDA), with an estimated duration of 18 months. We are eager to share our vision and technical prototypes, facilitate an open exchange of ideas, and encourage you to think big about the potential your expertise might bring to the table. We aim to achieve this through consolidated FAIR (Findable, Accessible, Interoperable, and Reusable) metadata and connected tools, expanding on previous work from ELIXIR and EMBL-EBI ( ). Through a community effort, we want to harness and mobilise the wealth of functional genomics and other genome–mapped datasets across projects, genomes and species, spanning across biomedical as well as biodiversity domains. These online meetings will start off the work of the new RDA Working Group on 'FAIRification of Genome Sequence Annotations'.
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