Abstract
Increasing interest in and experience with electronic health record (EHR)-driven phenotyping has yielded multiple challenges that are at present only partially addressed. Many solutions require the adoption of a single software platform, often with an additional cost of mapping existing patient and phenotypic data to multiple representations. We propose a set of guiding design principles and a modular software architecture to bridge the gap to a standardized phenotype representation, dissemination and execution. Ongoing development leveraging this proposed architecture has shown its ability to address existing limitations.
| Original language | English |
|---|---|
| Pages (from-to) | 147-151 |
| Number of pages | 5 |
| Journal | AMIA Summits on Translational Science Proceedings |
| Publication status | E-pub ahead of print - 25 Mar 2015 |
| Externally published | Yes |
Funding
This work has been supported in part by funding from PhEMA (R01 GM105688) and eMERGE (U01 HG006379, U01 HG006378 and U01 HG006388).