GET /api/v1/panels/
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

{
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            "version_created": "2019-04-25T15:33:30.887041Z",
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                "Adult solid tumours pertinent cancer susceptibility"
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                    "name": "GMS Cancer Germline Virtual",
                    "slug": "gms-cancer-germline-virtual",
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                    "description": "Cancer Germline 100K"
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            "version_created": "2018-12-11T12:56:38.497201Z",
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            "version_created": "2019-03-20T16:11:38.709137Z",
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            "hash_id": "58c7f3c78f620328d77ce70e",
            "name": "Amelogenesis imperfecta",
            "disease_group": "Skeletal disorders",
            "disease_sub_group": "Skeletal dysplasias",
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            "version_created": "2019-05-15T13:30:08.338755Z",
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                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            ]
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            "name": "Amyloidosis",
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            "version_created": "2019-02-02T15:49:34.689702Z",
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                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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                "number_of_genes": 30
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                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
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            "name": "Aniridia",
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            "version": "1.7",
            "version_created": "2019-03-20T17:04:02.268891Z",
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                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            "disease_sub_group": "Ocular malformations",
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            "version_created": "2019-03-25T16:30:32.499128Z",
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                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            "hash_id": "55b75d5b22c1fc05fd2345c9",
            "name": "Arthrogryposis",
            "disease_group": "Neurology and neurodevelopmental disorders",
            "disease_sub_group": "Neuromuscular disorders",
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            "version": "2.41",
            "version_created": "2019-05-03T16:46:08.796421Z",
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                    "slug": "gms-rare-disease",
                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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                    "name": "Component Of Super Panel",
                    "slug": "component-of-super-panel",
                    "description": "This panel is a component of a Super Panel"
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            "hash_id": null,
            "name": "Arthrogryposis - broad panel",
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            "version_created": "2019-05-03T16:46:11.484014Z",
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                "number_of_genes": 490
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                    "slug": "superpanel",
                    "description": "Superpanel"
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                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
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        },
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            "id": 477,
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            "name": "Ataxia and cerebellar anomalies - narrow panel",
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            "name": "Atypical haemolytic uraemic syndrome",
            "disease_group": "Renal and urinary tract disorders",
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                    "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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            "disease_sub_group": "Non-syndromic hearing loss",
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            "name": "Autism",
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                    "slug": "research",
                    "description": "This is a gene panel used for research."
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            "version_created": "2017-11-05T02:37:20.354821Z",
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            "name": "Bardet Biedl syndrome",
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            "version_created": "2019-03-15T13:35:36.713401Z",
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            "name": "Bladder cancer pertinent cancer susceptibility",
            "disease_group": "Cancer Programme",
            "disease_sub_group": "Pertinent cancer susceptibility gene panel",
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        },
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                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
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