Cargando…
POPDx: an automated framework for patient phenotyping across 392 246 individuals in the UK Biobank study
OBJECTIVE: For the UK Biobank, standardized phenotype codes are associated with patients who have been hospitalized but are missing for many patients who have been treated exclusively in an outpatient setting. We describe a method for phenotype recognition that imputes phenotype codes for all UK Bio...
Autores principales: | Yang, Lu, Wang, Sheng, Altman, Russ B |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846671/ https://www.ncbi.nlm.nih.gov/pubmed/36469791 http://dx.doi.org/10.1093/jamia/ocac226 |
Ejemplares similares
-
SAIL—a software system for sample and phenotype availability across biobanks and cohorts
por: Gostev, Mikhail, et al.
Publicado: (2011) -
Software Application Profile: PHESANT: a tool for performing automated phenome scans in UK Biobank
por: Millard, Louise AC, et al.
Publicado: (2018) -
Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics
por: McInnes, Gregory, et al.
Publicado: (2019) -
BiobankConnect: software to rapidly connect data elements for pooled analysis across biobanks using ontological and lexical indexing
por: Pang, Chao, et al.
Publicado: (2015) -
A platform for phenotyping disease progression and associated longitudinal risk factors in large-scale EHRs, with application to incident diabetes complications in the UK Biobank
por: Kim, Do Hyun, et al.
Publicado: (2023)