Cargando…
An extended set of yeast-based functional assays accurately identifies human disease mutations
We can now routinely identify coding variants within individual human genomes. A pressing challenge is to determine which variants disrupt the function of disease-associated genes. Both experimental and computational methods exist to predict pathogenicity of human genetic variation. However, a syste...
Autores principales: | Sun, Song, Yang, Fan, Tan, Guihong, Costanzo, Michael, Oughtred, Rose, Hirschman, Jodi, Theesfeld, Chandra L., Bansal, Pritpal, Sahni, Nidhi, Yi, Song, Yu, Analyn, Tyagi, Tanya, Tie, Cathy, Hill, David E., Vidal, Marc, Andrews, Brenda J., Boone, Charles, Dolinski, Kara, Roth, Frederick P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864455/ https://www.ncbi.nlm.nih.gov/pubmed/26975778 http://dx.doi.org/10.1101/gr.192526.115 |
Ejemplares similares
-
Identifying pathogenicity of human variants via paralog-based yeast complementation
por: Yang, Fan, et al.
Publicado: (2017) -
Fungal BLAST and Model Organism BLASTP Best Hits: new comparison resources at the Saccharomyces Genome Database (SGD)
por: Balakrishnan, Rama, et al.
Publicado: (2005) -
Overview of the COVID-19 text mining tool interactive demonstration track in BioCreative VII
por: Chatr-aryamontri, Andrew, et al.
Publicado: (2022) -
The BioGRID interaction database: 2015 update
por: Chatr-aryamontri, Andrew, et al.
Publicado: (2014) -
Expanded protein information at SGD: new pages and proteome browser
por: Nash, Robert, et al.
Publicado: (2007)