The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health

Author:

Walton Nephi A.,Hafen Brent,Graceffo Sara,Sutherland Nykole,Emmerson Melanie,Palmquist Rachel,Formea Christine M.ORCID,Purcell MaricelORCID,Heale Bret,Brown Matthew A.ORCID,Danford Christopher J.,Rachamadugu Sumathi I.,Person Thomas N.,Shortt Katherine A.,Christensen G. Bryce,Evans Jared M.,Raghunath Sharanya,Johnson Christopher P.,Knight Stacey,Le Viet T.ORCID,Anderson Jeffrey L.,Van Meter Margaret,Reading Teresa,Haslem Derrick S.,Hansen Ivy C.,Batcher Betsey,Barker Tyler,Sheffield Travis J.,Yandava Bhaskara,Taylor David P.,Ranade-Kharkar Pallavi,Giauque Christopher C.,Eyring Kenneth R.,Breinholt Jesse W.ORCID,Miller Mickey R.ORCID,Carter Payton R.,Gillman Jason L.,Gunn Andrew W.,Knowlton Kirk U.,Bonkowsky Joshua L.ORCID,Stefansson Kari,Nadauld Lincoln D.,McLeod Howard L.ORCID

Abstract

The clinical use of genomic analysis has expanded rapidly resulting in an increased availability and utility of genomic information in clinical care. We have developed an infrastructure utilizing informatics tools and clinical processes to facilitate the use of whole genome sequencing data for population health management across the healthcare system. Our resulting framework scaled well to multiple clinical domains in both pediatric and adult care, although there were domain specific challenges that arose. Our infrastructure was complementary to existing clinical processes and well-received by care providers and patients. Informatics solutions were critical to the successful deployment and scaling of this program. Implementation of genomics at the scale of population health utilizes complicated technologies and processes that for many health systems are not supported by current information systems or in existing clinical workflows. To scale such a system requires a substantial clinical framework backed by informatics tools to facilitate the flow and management of data. Our work represents an early model that has been successful in scaling to 29 different genes with associated genetic conditions in four clinical domains. Work is ongoing to optimize informatics tools; and to identify best practices for translation to smaller healthcare systems.

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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