Automated HL7v2 LRI informatics framework for streamlining genomics-EHR data integration

Author:

Dolin Robert H.,Gupta Rohan,Newsom Kimberly,Heale Bret S.E.,Gothi Shailesh,Starostik Petr,Chamala Srikar

Funder

University of Florida Health

Publisher

Elsevier BV

Subject

Computer Science Applications,Health Informatics,Pathology and Forensic Medicine

Reference24 articles.

1. Genomic data in the electronic health record;Walton;Adv Mol Pathol.,2019

2. Standards and guidelines for the interpretation and reporting of sequence variants in cancer;Li;J Mol Diagn JMD.,2017

3. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology;Richards;Genet Med Off J Am Coll Med Genet.,2015

4. vcf2fhir: a utility to convert VCF files into HL7 FHIR format for genomics-EHR integration;Dolin;BMC Bioinformatics.,2021

5. A pharmacogenomics clinical decision support service based on FHIR and CDS hooks;Dolin;Methods Inf Med.,2018

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