OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes
By David Tamborero, Abel Gonzalez-Perez, Núria López-Bigas. Bioinform., 2013
464 citations recorded by the source corpus.
Subfields: Cancer Research, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/a480afb61ec590a0dcb9d09f4c796ff69d115a6d
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- Gad Getz
- Matthew Meyerson
- Núria López-Bigas
- Abel Gonzalez-Perez
- M. Lawrence
- A. Gimenez-Roqueplo
- W. Marston Linehan
- D. Hoon
In Genetics
- Manel Esteller
- P. Park
- Hui Shen
- M. Wiznerowicz
- Feixiong Cheng
- Jill S. Barnholtz-Sloan
- Michael R. Stratton
- Christopher Sander
In Molecular Biology
- Manel Esteller
- Peter W. Laird
- Wanding Zhou
- P. Park
- Hui Shen
- Elaine R. Mardis
- Ilya Shmulevich
- Holger Heyn
Citations in the corpus
- A Landscape of Pharmacogenomic Interactions in Cancer (2016, methodology): “CGs were detected per cancer type by combining the outputs of three algorithms: MutSigCV, OncodriveFM, and OncodriveCLUST (Lawrence et al., 2013; Rubio-Perez et al., 2015; Tamborero et al., 2013a).”
- FunSeq2: a framework for prioritizing noncoding regulatory variants in cancer (2014, background): “Systematic studies of human cancer genomes have discovered a wide range of driver genes [2-6].”
- Variation Interpretation Predictors: Principles, Types, Performance, and Choice (2016, unknown): “OncodriveCLUST [Tamboreroetal.,2013]identifiesgenesthathavesignificantclus-tersofvariationsinproteins.”
- Comprehensive Characterization of Cancer Driver Genes and Mutations (2018, background): “OncodriveCLUST OncodriveCLUST (Tamborero et al., 2013a) identifies genes with non-silent mutations that cluster together in protein sequencemore than expected based on a background distribution of synonymous mutations.”
- Maftools: efficient and comprehensive analysis of somatic variants in cancer (2018, methodology): “To identify disease-associated cancer genes, we reimplemented OncodriveCLUST algorithm as previously described by Tamborero et al. (2013).”