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Paper Details

Sync for Genes Phase 5: Computable artifacts for sharing dynamically annotated FHIR-formatted genomic variants.
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2023
FHIR, FHIR-encoded variants, FHIR-formatted genomic variants, Genes, PharmGKB, biomedical knowledge artifacts, clinicians, computable, patient
Author NameAffiliation
Robert Dolin
Bret S E Heale
Rohan GuptaShri Mata Vaishno Devi University Katra India.
Carla Alvarez
Justin AronsonNorthwestern University Evanston Illinois USA.
Aziz A Boxwala
Shaileshbhai R GothiUniversity of Florida Gainesville Florida USA.
Ammar HusamiCincinnati Children's Hospital Medical Center Cincinnati Ohio USA.
James Shalaby
Lawrence BabbMedical and Population Genetics Broad Institute of MIT and Harvard Cambridge Massachusetts USA.
Alex H WagnerNationwide Children's Hospital/OSU Columbus Ohio USA.
Srikar ChamalaUSC/Children's Hospital Los Angeles Los Angeles California USA.
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink