Enabling precision medicine via standard communication of HTS provenance, analysis, and results

A personalized approach based on a patient's or pathogen’s unique genomic sequence is the foundation of precision medicine. Genomic findings must be robust and reproducible, and experimental data capture should adhere to findable, accessible, interoperable, and reusable (FAIR) guiding principle...

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Detalles Bibliográficos
Autores principales: Alterovitz, Gil, Dean, Dennis, Goble, Carole, Crusoe, Michael R., Soiland-Reyes, Stian, Bell, Amanda, Hayes, Anais, Suresh, Anita, Purkayastha, Anjan, King, Charles H., Taylor, Dan, Johanson, Elaine, Thompson, Elaine E., Donaldson, Eric, Morizono, Hiroki, Tsang, Hsinyi, Vora, Jeet K., Goecks, Jeremy, Yao, Jianchao, Almeida, Jonas S., Keeney, Jonathon, Addepalli, KanakaDurga, Krampis, Konstantinos, Smith, Krista M., Guo, Lydia, Walderhaug, Mark, Schito, Marco, Ezewudo, Matthew, Guimera, Nuria, Walsh, Paul, Kahsay, Robel, Gottipati, Srikanth, Rodwell, Timothy C., Bloom, Toby, Lai, Yuching, Simonyan, Vahan, Mazumder, Raja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Community Page
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338479/
https://www.ncbi.nlm.nih.gov/pubmed/30596645
http://dx.doi.org/10.1371/journal.pbio.3000099

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338479/
https://www.ncbi.nlm.nih.gov/pubmed/30596645
http://dx.doi.org/10.1371/journal.pbio.3000099

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