Tools developed by the NBRCIT are open source and are available to download on this page.
ODIN:
During our work in the Rare Diseases research domain we have come across the problem of importing large amounts of legacy and laboratory data from projects. We have developed a data mapping and importing tool OpenClinica Data Importer web ApplicatioN “ODIN” which comes with a user-friendly web interface. ODIN uses the OpenClinica SOAP web services to import subjects and their clinical data into OpenClinica, leaving the OpenClinica audit trail intact. A interface makes the importer easy to use.
Please download the source files from HERE.
User documentation for ODIN: ODINEndUserDocumentation
Panogram – OC integration:
Within the area of Rare Diseases collecting accurate pedigree information is essential as 80% of Rare Diseases are genetic in origin. We have integrated Panogram, a standalone Pedigree drawing tool based on the Phenotips platform, into OpenClinica to allow clinicians to draw pedigrees online.
Camfetch:
Camfetch is a list of predefined javascript (jQuery) functions that can be included in a CRF. We use camfetch to call our custom services such as Panogram or different lookup services (ontology, medication, etc).