Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging

Genome sequencing has established clinical utility for rare disease diagnosis. While increasing numbers of individuals have undergone elective genome sequencing, a comprehensive study surveying genome-wide disease-associated genes in adults with deep phenotyping has not been reported. Here we report...

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Detalles Bibliográficos
Autores principales: Hou, Ying-Chen Claire, Yu, Hung-Chun, Martin, Rick, Cirulli, Elizabeth T., Schenker-Ahmed, Natalie M., Hicks, Michael, Cohen, Isaac V., Jönsson, Thomas J., Heister, Robyn, Napier, Lori, Swisher, Christine Leon, Dominguez, Saints, Tang, Haibao, Li, Weizhong, Perkins, Bradley A., Barea, Jaime, Rybak, Christina, Smith, Emily, Duchicela, Keegan, Doney, Michael, Brar, Pamila, Hernandez, Nathaniel, Kirkness, Ewen F., Kahn, Andrew M., Venter, J. Craig, Karow, David S., Caskey, C. Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
PNAS Plus
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022190/
https://www.ncbi.nlm.nih.gov/pubmed/31980526
http://dx.doi.org/10.1073/pnas.1909378117

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022190/
https://www.ncbi.nlm.nih.gov/pubmed/31980526
http://dx.doi.org/10.1073/pnas.1909378117

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