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1.
Brief Bioinform ; 18(3): 479-487, 2017 05 01.
Artículo en Inglés | MEDLINE | ID: mdl-27016392

RESUMEN

Electronic access to multiple data types, from generic information on biological systems at different functional and cellular levels to high-throughput molecular data from human patients, is a prerequisite of successful systems medicine research. However, scientists often encounter technical and conceptual difficulties that forestall the efficient and effective use of these resources. We summarize and discuss some of these obstacles, and suggest ways to avoid or evade them.The methodological gap between data capturing and data analysis is huge in human medical research. Primary data producers often do not fully apprehend the scientific value of their data, whereas data analysts maybe ignorant of the circumstances under which the data were collected. Therefore, the provision of easy-to-use data access tools not only helps to improve data quality on the part of the data producers but also is likely to foster an informed dialogue with the data analysts.We propose a means to integrate phenotypic data, questionnaire data and microbiome data with a user-friendly Systems Medicine toolbox embedded into i2b2/tranSMART. Our approach is exemplified by the integration of a basic outlier detection tool and a more advanced microbiome analysis (alpha diversity) script. Continuous discussion with clinicians, data managers, biostatisticians and systems medicine experts should serve to enrich even further the functionality of toolboxes like ours, being geared to be used by 'informed non-experts' but at the same time attuned to existing, more sophisticated analysis tools.


Asunto(s)
Inflamación , Investigación Biomédica , Humanos , Análisis de Sistemas
2.
Stud Health Technol Inform ; 253: 75-79, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30147044

RESUMEN

This paper examines the relevance of genetic pedigree data in the context of medical research platforms. By surveying currently available tools for visualization and analysis of this data type and by considering possible use cases that could make usage of the combination of singular patient data and pedigree data, the advantages of integrating the data type into a medical research platform were shown. In a practical work step, an integration procedure of pedigree data into tranSMART was created. Furthermore, a tool to analyze and visualize pedigree data in combination with other patient data was implemented into SmartR, a dynamic analysis tool inside of tranSMART. Finally, we address limitations and future development strategies of the tool.


Asunto(s)
Linaje , Programas Informáticos , Investigación Biomédica , Humanos , Estadística como Asunto
3.
Stud Health Technol Inform ; 228: 262-6, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27577384

RESUMEN

In University Medical Centers, heterogeneous data are generated that cannot always be clearly attributed to patient care or biomedical research. Each data set has to adhere to distinct intrinsic and operational quality standards. However, only if high-quality data, tools to work with the data, and most importantly guidelines and rules of how to work with the data are addressed adequately, an infrastructure can be sustainable. Here, we present the IT Research Architecture of the University Medical Center Göttingen and describe our ten years' experience and lessons learned with infrastructures in networked medical research.


Asunto(s)
Investigación Biomédica , Informática Médica , Centros Médicos Académicos , Investigación Biomédica/organización & administración , Intercambio de Información en Salud , Humanos , Informática Médica/organización & administración
4.
Stud Health Technol Inform ; 205: 848-52, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25160307

RESUMEN

Biomedical research projects show an increasing demand of large numbers of participants from different recruiting centers to achieve statistically significant results. The collected types of data are stored in distributed databases and are linked to the participant by different non-resolvable identifiers (layered pseudonyms) for de-identification. To ensure the quality of the gathered data, regular quality assurance analyses are required at each local center. Because of the distributed databases and layered pseudonyms the analyses can only be achieved manually. Therefore, the process is error-prone and laborious. The objective of this paper is to propose a solution concept to automate the manual process by using a local study participant management system. It orchestrates the process and enables the quality assurance analyses within a clinical data warehouse.


Asunto(s)
Investigación Biomédica/normas , Participación de la Comunidad , Seguridad Computacional/normas , Confidencialidad/normas , Registros Electrónicos de Salud/normas , Almacenamiento y Recuperación de la Información/normas , Registro Médico Coordinado/normas , Alemania , Garantía de la Calidad de Atención de Salud/normas
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