Cargando…
The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations
Objective: This paper describes the Precision Medicine Knowledge Base (PMKB; https://pmkb.weill.cornell.edu), an interactive online application for collaborative editing, maintenance, and sharing of structured clinical-grade cancer mutation interpretations. Materials and Methods: PMKB was built usin...
Autores principales: | Huang, Linda, Fernandes, Helen, Zia, Hamid, Tavassoli, Peyman, Rennert, Hanna, Pisapia, David, Imielinski, Marcin, Sboner, Andrea, Rubin, Mark A, Kluk, Michael, Elemento, Olivier |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5391733/ https://www.ncbi.nlm.nih.gov/pubmed/27789569 http://dx.doi.org/10.1093/jamia/ocw148 |
Ejemplares similares
-
Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care
por: Rennert, Hanna, et al.
Publicado: (2016) -
Personal Cancer Genome Reporter: variant interpretation report for precision oncology
por: Nakken, Sigve, et al.
Publicado: (2018) -
EthSEQ: ethnicity annotation from whole exome sequencing data
por: Romanel, Alessandro, et al.
Publicado: (2017) -
Deep Convolutional Neural Networks Enable Discrimination of Heterogeneous Digital Pathology Images
por: Khosravi, Pegah, et al.
Publicado: (2017) -
Whole-genome characterization of myoepithelial carcinomas of the soft tissue
por: Cyrta, Joanna, et al.
Publicado: (2022)