Demo Applications

Genomics Advisor
Variant Mapper


Genomics Advisor

The SMART Genomics Advisor represents a first in terms of genomic integration into Electronic Health Records (EHRs) and Personal Health Records (PHRs). Its robustness and interoperability with a wide variety of systems is done through the SMART framework and allows clinicians to easily access relevant clinical and genomic information across a variety of EHR/PHRs. The application supports integration of clinical and genomic data from SMART-enabled service.



Variant Mapper

Variant Mapper demonstrates how genomics can be integrated into clinical decision support. Comparing patients' DNA variants and those from a database documenting genotype-phenotype assoction (in this case, Clinvar), this application alerts clinicians about potential risk factors. By the dynamically binding the knowledge database and patients' genotype, the application also allows its clinicians to learn more about their patients as the database grows.

Variant Mapper: taking reads as input from Yishen Chen on Vimeo.