grant
Southeastern Genomic Medicine eConsult Network (SeGMeNt)
Organization UNIV OF NORTH CAROLINA CHAPEL HILLLocation CHAPEL HILL, UNITED STATESPosted 10 Apr 2026Deadline 31 Mar 2028
NIHUS FederalResearch GrantFY2026AI technologyAcademic Medical CentersAddressAdministratorAdoptionAffectAreaAssess implementationAssessment instrumentAssessment toolCancersCaringCharacteristicsChromosomal DisordersChromosome Abnormality DisordersChromosome DisordersClientClinicalClinical geneticsCollaborationsCommunicationCommunitiesComplexCongenital chromosomal diseaseConsultConsultationsCounselingDNA mutationData AnalysesData AnalysisDiagnosisDiagnosticDisciplineEHR systemEducationEducational aspectsElectronic Health RecordElectronicsEvaluationExploration, Preparation, Implementation, and SustainabilityExploration, Preparation, Implementation, and SustainmentFutureGeneticGenetic ChangeGenetic DiseasesGenetic DiversityGenetic VariationGenetic defectGenetic mutationGenomic approachGenomic medicineGenomicsHealthHealth CareHealth Care ProvidersHealth Care SystemsHealth PersonnelHealth StatusHealth systemHistoryImplementation assessmentIndividualInformaticsInterviewKnowledgeLearningLegalLevel of HealthLinkMalignant NeoplasmsMalignant TumorMedical GeneticsMendelian diseaseMendelian disorderMendelian genetic disorderMethodsModelingModernizationMutationNorth CarolinaOrphan DiseaseOut-patientsOutcomeOutpatientsPatient CarePatient Care DeliveryPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatientsPatternPersonsPharmacogenomicsPhysiciansPopulationPrimary CareProgram EvaluationProviderQOLQuality of lifeRare DiseasesRare DisorderRecommendationRecording of previous eventsResearchRoleScreening ResultSecureServicesSightSouth CarolinaSpecialistSpecific qualifier valueSpecifiedSurvey InstrumentSurveysSystemTechnologyTestingTimeTransmissionTravelUniversity Medical CentersVisionVisitWait Timeartificial intelligence technologybarriers to implementationcare for patientscare of patientscaring for patientsclinical research siteclinical sequencingclinical siteclinician communicationcommunicate to clinicianscommunicate to providerscommunicate with clinicianscommunicate with doctorscommunicate with providersconsultationconsultsdata interpretationdata standardizationdata standardsdepositorydesigndesigningdoctor communicationelectronicelectronic deviceelectronic health care recordelectronic health medical recordelectronic health plan recordelectronic health record systemelectronic health registryelectronic medical health recordevaluate implementationevaluation of implementationgene testinggene-based testinggenetic conditiongenetic disordergenetic resultsgenetic testinggenetic testing resultsgenome medicinegenome mutationgenomic aberrationsgenomic effortgenomic strategyhealth care personnelhealth care workerhealth levelhealth providerhealth staffhealth workershealth workforcehealthcare employeeshealthcare staffhealthcare workforcehistorieshuman diseaseimplementation barriersimplementation challengesimplementation evaluationimplementation frameworkimplementation outcomesimplementation research frameworkimplementation scienceimplementation science frameworkimprovedimproved outcomeinformatics infrastructureinterestmalignancymedical care providersmedical personnelmembermonogenic diseasemonogenic disordermortalityneoplasm/cancernew technologynovelnovel technologiesorphan disorderoutreachpatient oriented outcomesprenatalpreventpreventingprovider communicationprovider to providerrare conditionrare syndromerepositoryresponsesatisfactionscreeningscreeningssingle-gene diseasesingle-gene disordersocial roletherapy optimizationtooltransmission processtreatment optimizationtreatment providertumorunbornunder served areaunder served geographic areaunder served locationunder served regionunderserved areaunderserved geographic areaunderserved locationunderserved regionuser centered designvirtual carevirtual health carevisual function
Description preview
Advances in our understanding of the role of genetic variation in human diseases and the technologies for genomic analysis and therapy have the potential to revolutionize health care. Clinical sequencing has become a routine tool for diagnosis of patients with rare monogenic diseases, pharmacogenomics is increasingly used to optimize therapy, and…
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