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09:37 min
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August 15, 2019
DOI:
1Program in Developmental Biology,Baylor College of Medicine, 2Medical Scientist Training Program,Baylor College of Medicine, 3Department of Pediatrics,Baylor College of Medicine, 4Jan and Dan Duncan Neurological Research Institute,Texas Children’s Hospital, 5Department of Molecular and Human Genetics,Baylor College of Medicine, 6Department of Neuroscience,Baylor College of Medicine, 7Howard Hughes Medical Institute,Baylor College of Medicine
Summary
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Aquí, presentamos un protocolo para acceder y analizar muchas bases de datos de organismos humanos y modelo de manera eficiente. Este protocolo demuestra el uso de MARRVEL para analizar las variantes que causan la enfermedad candidata identificadas a partir de los esfuerzos de secuenciación de próxima generación.
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Cite this Article
Wang, J., Liu, Z., Bellen, H. J., Yamamoto, S. Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information. J. Vis. Exp. (150), e59542, doi:10.3791/59542 (2019).
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