Ontologizing health systems data at scale: making translational discovery a reality.
Ontologizing health systems data at scale: making translational discovery a reality.
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DOI:
10.1038/s41746-023-00830-x
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发表时间:
2023-05-19
影响因子:
15.2
通讯作者:
Kahn, Michael G.
中科院分区:
文献类型:
--
作者:
Callahan, Tiffany J.;Stefanski, Adrianne L.;Wyrwa, Jordan M.;Zeng, Chenjie;Ostropolets, Anna;Banda, Juan M.;Baumgartner, William A., Jr.;Boyce, Richard D.;Casiraghi, Elena;Coleman, Ben D.;Collins, Janine H.;Davies, Sara J. Deakyne;Feinstein, James A.;Lin, Asiyah Y.;Martin, Blake;Matentzoglu, Nicolas A.;Meeker, Daniella;Reese, Justin;Sinclair, Jessica;Taneja, Sanya B.;Trinkley, Katy E.;Vasilevsky, Nicole A.;Williams, Andrew E.;Zhang, Xingmin A.;Denny, Joshua C.;Ryan, Patrick B.;Hripcsak, George;Bennett, Tellen D.;Haendel, Melissa A.;Robinson, Peter N.;Hunter, Lawrence E.;Kahn, Michael G.
Common data models solve many challenges of standardizing electronic health record (EHR) data but are unable to semantically integrate all of the resources needed for deep phenotyping. Open Biological and Biomedical Ontology (OBO) Foundry ontologies provide computable representations of biological knowledge and enable the integration of heterogeneous data. However, mapping EHR data to OBO ontologies requires significant manual curation and domain expertise. We introduce OMOP2OBO, an algorithm for mapping Observational Medical Outcomes Partnership (OMOP) vocabularies to OBO ontologies. Using OMOP2OBO, we produced mappings for 92,367 conditions, 8611 drug ingredients, and 10,673 measurement results, which covered 68–99% of concepts used in clinical practice when examined across 24 hospitals. When used to phenotype rare disease patients, the mappings helped systematically identify undiagnosed patients who might benefit from genetic testing. By aligning OMOP vocabularies to OBO ontologies our algorithm presents new opportunities to advance EHR-based deep phenotyping.
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DOI:
10.1126/science.aal4043
发表时间:
2018-03-16
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Bastarache L;Hughey JJ;Hebbring S;Marlo J;Zhao W;Ho WT;Van Driest SL;McGregor TL;Mosley JD;Wells QS;Temple M;Ramirez AH;Carroll R;Osterman T;Edwards T;Ruderfer D;Velez Edwards DR;Hamid R;Cogan J;Glazer A;Wei WQ;Feng Q;Brilliant M;Zhao ZJ;Cox NJ;Roden DM;Denny JC
通讯作者:
Denny JC
DOI:
10.1146/annurev-genom-090314-024956
发表时间:
2016-08-31
影响因子:
8.7
作者:
Denny JC;Bastarache L;Roden DM
通讯作者:
Roden DM
影响因子:
11.1
作者:
Deer RR;Rock MA;Vasilevsky N;Carmody L;Rando H;Anzalone AJ;Basson MD;Bennett TD;Bergquist T;Boudreau EA;Bramante CT;Byrd JB;Callahan TJ;Chan LE;Chu H;Chute CG;Coleman BD;Davis HE;Gagnier J;Greene CS;Hillegass WB;Kavuluru R;Kimble WD;Koraishy FM;Köhler S;Liang C;Liu F;Liu H;Madhira V;Madlock-Brown CR;Matentzoglu N;Mazzotti DR;McMurry JA;McNair DS;Moffitt RA;Monteith TS;Parker AM;Perry MA;Pfaff E;Reese JT;Saltz J;Schuff RA;Solomonides AE;Solway J;Spratt H;Stein GS;Sule AA;Topaloglu U;Vavougios GD;Wang L;Haendel MA;Robinson PN
通讯作者:
Robinson PN
DOI:
10.1093/jamia/ocz179
发表时间:
2019-12-01
影响因子:
6.4
作者:
Bastarache, Lisa;Hughey, Jacob J.;Denny, Joshua C.
通讯作者:
Denny, Joshua C.
影响因子:
4.5
作者:
Lin, M. C.;Vreeman, D. J.;McDonald, Clement J.;Huff, S. M.
通讯作者:
Huff, S. M.