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2.
Genome Biol ; 15(3): R53, 2014 Mar 25.
Artículo en Inglés | MEDLINE | ID: mdl-24667040

RESUMEN

BACKGROUND: There is tremendous potential for genome sequencing to improve clinical diagnosis and care once it becomes routinely accessible, but this will require formalizing research methods into clinical best practices in the areas of sequence data generation, analysis, interpretation and reporting. The CLARITY Challenge was designed to spur convergence in methods for diagnosing genetic disease starting from clinical case history and genome sequencing data. DNA samples were obtained from three families with heritable genetic disorders and genomic sequence data were donated by sequencing platform vendors. The challenge was to analyze and interpret these data with the goals of identifying disease-causing variants and reporting the findings in a clinically useful format. Participating contestant groups were solicited broadly, and an independent panel of judges evaluated their performance. RESULTS: A total of 30 international groups were engaged. The entries reveal a general convergence of practices on most elements of the analysis and interpretation process. However, even given this commonality of approach, only two groups identified the consensus candidate variants in all disease cases, demonstrating a need for consistent fine-tuning of the generally accepted methods. There was greater diversity of the final clinical report content and in the patient consenting process, demonstrating that these areas require additional exploration and standardization. CONCLUSIONS: The CLARITY Challenge provides a comprehensive assessment of current practices for using genome sequencing to diagnose and report genetic diseases. There is remarkable convergence in bioinformatic techniques, but medical interpretation and reporting are areas that require further development by many groups.


Asunto(s)
Bases de Datos Genéticas/normas , Pruebas Genéticas/métodos , Genómica/métodos , Revisión de la Investigación por Pares , Análisis de Secuencia de ADN/métodos , Niño , Femenino , Organización de la Financiación , Pruebas Genéticas/economía , Pruebas Genéticas/normas , Genómica/economía , Genómica/normas , Cardiopatías Congénitas/diagnóstico , Cardiopatías Congénitas/genética , Humanos , Masculino , Miopatías Estructurales Congénitas/diagnóstico , Miopatías Estructurales Congénitas/genética , Análisis de Secuencia de ADN/economía , Análisis de Secuencia de ADN/normas
3.
Health Aff (Millwood) ; 28(2): 390-2, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19275994

RESUMEN

Electronic medical records and personal health records have made good progress in reducing costs and inefficiencies, but the key to building a health care delivery system for the twenty-first century is to evolve toward personal health management systems that apply the full power of software to improve patient care. Such systems can enable better outcomes and improve the satisfaction of consumers and providers alike. Through technology innovation, sensible policy approaches, and industrywide collaboration, we can empower individuals to take control of their health while enabling providers and payers to broaden access to higher-quality, more affordable care.


Asunto(s)
Registros Electrónicos de Salud/organización & administración , Registros de Salud Personal , Calidad de la Atención de Salud , Eficiencia Organizacional , Humanos , Gestión de la Información , Atención Dirigida al Paciente , Programas Informáticos
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