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Presentation
The platform is made up of three IT engineers. The platform develops methods to accelerate translational research between doctors and researchers, between the hospital and the institute. We create software allowing the storage and analysis of patients’ phenotypic data.
Phenotypic and genetic databases
The aim is to help researchers and clinicians to collect, pool, structure, sustain and secure patient data for local, national or international studies. We developed the "eCohorte" software to quickly set up a database containing all the necessary tools for data entry and retrieval. We now manage 82 databases with a total of 131,000 patients. Much of this work also involves the automated retrieval and load of retrospective data.
The transversal tools
We have developed several tools for researchers, clinicians and managers: BioPancarte for personalized visualization of laboratory results, Auxo for the creation of growth curves, Gecko for the management of clinical studies and inclusions of Patient, Gene2CT for automatic monitoring of clinical trials associated with genetic mutations etc. These software are deposited to the Agency of Protection of the Programs.
Biomedical data warehouse
We developed Dr. Warehouse, a biomedical data warehouse that integrates free text data (hospitalization, consultation, prescription reports, etc.) as well as coded data (biological results). Dr Warehouse is implemented in Necker-Enfants Malades hospital. We loaded 4 million documents from 20 different sources (EHR, Biomedical databases) from 1996 to 2017 for 480,000 patients. It also contains 36 million biological results. The main functionalities are to be able to search patients using a 'Google like' search engine, to be able to carry out automatic phenotypic descriptions, and to propose tools to help diagnosis by similarity calculation between patients. Dr. Warehouse's interface provides physicians with ergonomic tools to explore medical records to accelerate the recruitment of patients into clinical studies. Dr Warehouse is now also released under the GNU GPL (open source License).
Team
Resources & publications
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Journal (source)J Biomed Inform
Phenotypic similarity for rare disease: Ciliopathy diagnoses and subtyping.
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Journal (source)Blood
Pediatric Evans syndrome is associated with a high frequency of potentially d...
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Journal (source)Orphanet journal of rare diseases
Next Generation Phenotyping Using Narrative Reports in a Rare Disease Clinica...
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Journal (source)Journal of biomedical informatics
A Clinician Friendly Data Warehouse Oriented Toward Narrative Reports: Dr. Wa...
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Journal (source)Journal of biomedical informatics
Finding Patients Using Similarity Measures in a Rare Diseases-Oriented Clinic...