{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Schuler BA"],"funding":["NHLBI NIH HHS","NHGRI NIH HHS","NINDS NIH HHS"],"pagination":["e154942"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8970663"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["132(7)"],"pubmed_abstract":["Rare genetic disorders, when considered together, are relatively common. Despite advancements in genetics and genomics technologies as well as increased understanding of genomic function and dysfunction, many genetic diseases continue to be difficult to diagnose. The goal of this Review is to increase the familiarity of genetic testing strategies for non-genetics providers. As genetic testing is increasingly used in primary care, many subspecialty clinics, and various inpatient settings, it is important that non-genetics providers have a fundamental understanding of the strengths and weaknesses of various genetic testing strategies as well as develop an ability to interpret genetic testing results. We provide background on commonly used genetic testing approaches, give examples of phenotyp"],"journal":["The Journal of clinical investigation"],"pubmed_title":["Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases."],"pmcid":["PMC8970663"],"funding_grant_id":["U01 NS134349","U01 HG007674","R38 HL143619"],"pubmed_authors":["Koziura M","Hamid R","Phillips JA","Schuler BA","Cogan JD","Nelson ET"],"additional_accession":[]},"is_claimable":false,"name":"Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases.","description":"Rare genetic disorders, when considered together, are relatively common. Despite advancements in genetics and genomics technologies as well as increased understanding of genomic function and dysfunction, many genetic diseases continue to be difficult to diagnose. The goal of this Review is to increase the familiarity of genetic testing strategies for non-genetics providers. As genetic testing is increasingly used in primary care, many subspecialty clinics, and various inpatient settings, it is important that non-genetics providers have a fundamental understanding of the strengths and weaknesses of various genetic testing strategies as well as develop an ability to interpret genetic testing results. We provide background on commonly used genetic testing approaches, give examples of phenotyp","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Apr","modification":"2025-04-26T13:06:12.933Z","creation":"2025-04-06T14:07:09.84Z"},"accession":"S-EPMC8970663","cross_references":{"pubmed":["35362483"],"doi":["10.1172/JCI154942"]}}