Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Clinical trials are typically conducted over a population within a defined time period in order to illuminate certain characteristics of a health issue or disease process. These cross-sectional studies give us a 'snapshot' of this disease process over a large number of people but do not allow us to model the temporal nature of disease, thereby allowing for modelling detailed prognostic predictions. The aim of this paper is to explore an extension of the temporal bootstrap to identify intermediate stages in a disease process and sub-categories of the disease exhibiting subtly different symptoms. Our approach is compared to a strawman method and investigated in its ability to explain the dynamics of progression on biomedical data from three diseases: Glaucoma, Breast Cancer and Parkinson's disease. We focus on creating reliable time-series models from large amounts of historical cross-sectional data using the temporal bootstrap technique. Two issues are explored: how to build time-series models from cross-sectional data, and how to automatically identify different disease states along these trajectories, as well as the transitions between them. Our approach of relabeling trajectories allows us to explore the temporal nature of how diseases progress even when time-series data is not available (if the cross-sectional study is large enough). We intend to expand this research to deal with multiple studies where we can combine both cross-sectional and longitudinal datasets and to focus on the junctions of the trajectories as key stages in the progression of disease.
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Source |
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http://dx.doi.org/10.1016/j.jbi.2012.11.003 | DOI Listing |
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