| Literature DB >> 20443924 |
Andreas C Mauer1, Edward M Barbour, Nickolay A Khazanov, Natasha Levenkova, Shamim A Mollah, Barry S Coller.
Abstract
The lack of standardized methods for human phenotyping is a major obstacle in translational science. We have developed a bleeding history phenotyping system comprising an ontology, a questionnaire, a Web-based phenotype recording instrument (PRI), and a database. The ontology facilitates transparency, collaboration, aggregation of data, and data analysis. The integrated system allows investigators worldwide to use the PRI, add their de-identified data to the database, and query the aggregated data. Thus, this system can increase the power to detect genotype-phenotype-environment relationships and help new investigators begin their studies. We anticipate that this approach may be applicable to other disorders.Entities:
Mesh:
Year: 2009 PMID: 20443924 PMCID: PMC5350758 DOI: 10.1111/j.1752-8062.2009.00147.x
Source DB: PubMed Journal: Clin Transl Sci ISSN: 1752-8054 Impact factor: 4.689