{"rating_data": {"avg_stars": 0, "total": 0, "avg": 0}, "name": "DECIPHER (DatabasE of Genomic variants and Phenotype in Humans Using Ensembl Resources)", "created": "2014-10-22 23:57:26", "url": "https://decipher.sanger.ac.uk/search?q={{symbol}}", "lastmodified": "2014-10-22 23:57:26", "usage_data": {"layouts": 3.0, "users": 3}, "popularity": 3.0, "owner": {"username": "asu", "url": "/profile/3/asu", "name": "Andrew Su"}, "species": ["human"], "shortUrl": "decipher.sanger.ac.uk", "id": 1169, "short_description": "DECIPHER is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants", "role_permission": ["biogpsusers"], "permission_style": "public", "type": "iframe", "options": null, "tags": ["variants"], "description": "DECIPHER (DatabasE of Genomic variants and Phenotype in Humans Using Ensembl Resources) is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants.\n\nDECIPHER enhances clinical diagnosis by retrieving information from a variety of bioinformatics resources relevant to the variant found in the patient. The patient's variant is displayed in the context of both normal variation and pathogenic variation reported at that locus thereby facilitating interpretation.\n\n\n\nhttps://decipher.sanger.ac.uk/\n"}