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European Genome-phenome Archive (EGA) is a repository for human biomolecular and phenotypic data [1] in the United Kingdom and Spain. [2] [3] It involves the secure storage of all potentially identifiable genetic data, phenotypic and clinical data generated by biomedical research programs.
The German Human Genome-Phenome Archive (GHGA) is a consortium within the national data infrastructure (NFDI).GHGA aims to create a secure national data infrastructure for human omics data in order to make these data available for scientific research while preventing the misuse of data.
International Human Epigenome Consortium: [28] integrates epigenomic reference data from well-known national endeavors such as the Canadian CEEHRC, [29] European Blueprint, [30] European Genome-phenome Archive (EGA [31]), US ENCODE and NIH Roadmap, German DEEP, [32] Japanese CREST, [33] Korean KNIH, Singapore's GIS and China's EpiHK [34]
The European Nucleotide Archive, European Variation Archive, and European Genome-phenome Archive at EMBL-EBI [3] EUCANCan [10] European Joint Programme on Rare Diseases [11] Genomics England [12] Human Cell Atlas [12] Human Heredity and Health in Africa (H3Africa) [13] International Cancer Genome Consortium - ARGO [12] Matchmaker Exchange [12]
The data produced are made freely available to the research community via the IHEC Data Portal, [31] [32] European Genome-phenome Archive (EGA), [33] and other venues. [34] [25] [35] In addition, participating research projects are engaged in developing new epigenomics and associated bioinformatics methods.
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At the headquarters in Heidelberg, there are units in cell biology and biophysics, developmental biology, genome biology, and structural and computational biology, as well as service groups complementing the aforementioned research fields. Many scientific breakthroughs have been made at EMBL.
Saccharomyces cerevisiae was the first eukaryotic organism to have its complete genome sequence determined.. This list of "sequenced" eukaryotic genomes contains all the eukaryotes known to have publicly available complete nuclear and organelle genome sequences that have been sequenced, assembled, annotated and published; draft genomes are not included, nor are organelle-only sequences.