{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"study_type":["Exome Sequencing"],"full_dataset_link":["https://ega-archive.org/studies/EGAS00001005764"],"host":["EGA"],"description":["EGA study EGAS00001005764"],"dataset_title":["Germline loss-of-function P2RY8 variants in SLE"],"repository":["EGA"],"category":["restricted"],"additional_accession":[]},"is_claimable":false,"name":"JEM 20211004R","description":"Our mission is to undertake ground breaking research, combining fundamental science and strong clinical interactions, to uncover the mechanism of disease of our patients, ultimately to provide a diagnosis and improved treatments. SLE is an autoimmune disease with a strong genetic component. Genome-wide association studies (GWAS) have revealed that multiple common variants confer genetic susceptibility to SLE, defining key pathways involved in disease pathogenesis.","dates":{"updated":"2021-11-16 13:33:21"},"accession":"EGAS00001005764","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAD00001008330","EGAC00001002394"]}}