SSA-ME Detection of cancer driver genes using mutual exclusivity by small subnetwork analysis
暂无分享,去创建一个
Kathleen Marchal | Bram Weytjens | Sergio Pulido-Tamayo | K. Marchal | Dries De Maeyer | Sergio Pulido-Tamayo | Bram Weytjens | Dries De Maeyer | D. De Maeyer
[1] C. Sander,et al. Predicting the functional impact of protein mutations: application to cancer genomics , 2011, Nucleic acids research.
[2] David Haussler,et al. PARADIGM-SHIFT predicts the function of mutations in multiple cancers using pathway impact analysis , 2012, Bioinform..
[3] T. Hubbard,et al. A census of human cancer genes , 2004, Nature Reviews Cancer.
[4] A. Gonzalez-Perez,et al. Functional impact bias reveals cancer drivers , 2012, Nucleic acids research.
[5] L. Marchionni,et al. Dysregulation of EGFR Pathway in EphA2 Cell Subpopulation Significantly Associates with Poor Prognosis in Colorectal Cancer , 2016, Clinical Cancer Research.
[6] P. Bork,et al. A method and server for predicting damaging missense mutations , 2010, Nature Methods.
[7] Haiyuan Yu,et al. HINT: High-quality protein interactomes and their applications in understanding human disease , 2012, BMC Systems Biology.
[8] Henning Hermjakob,et al. The Reactome pathway knowledgebase , 2013, Nucleic Acids Res..
[9] Benjamin J. Raphael,et al. Mutational landscape and significance across 12 major cancer types , 2013, Nature.
[10] Steven A. Roberts,et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes , 2013 .
[11] Cheng-Wen Wu,et al. The Emerging Role of SOX2 in Cell Proliferation and Survival and Its Crosstalk with Oncogenic Signaling in Lung Cancer , 2013, Stem cells.
[12] J. Shendure,et al. A general framework for estimating the relative pathogenicity of human genetic variants , 2014, Nature Genetics.
[13] Joshua M. Stuart,et al. The Cancer Genome Atlas Pan-Cancer analysis project , 2013, Nature Genetics.
[14] R Tibshirani,et al. Combined microarray analysis of small cell lung cancer reveals altered apoptotic balance and distinct expression signatures of MYC family gene amplification , 2006, Oncogene.
[15] G. Getz,et al. GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers , 2011, Genome Biology.
[16] Nuria Lopez-Bigas,et al. Gitools: Analysis and Visualisation of Genomic Data Using Interactive Heat-Maps , 2011, PloS one.
[17] Eli Upfal,et al. De Novo Discovery of Mutated Driver Pathways in Cancer , 2011, RECOMB.
[18] Gary D Bader,et al. International network of cancer genome projects , 2010, Nature.
[19] Bridget E. Begg,et al. A Proteome-Scale Map of the Human Interactome Network , 2014, Cell.
[20] W. Hahn,et al. Modelling the molecular circuitry of cancer , 2002, Nature Reviews Cancer.
[21] Benjamin J. Raphael,et al. Pan-Cancer Network Analysis Identifies Combinations of Rare Somatic Mutations across Pathways and Protein Complexes , 2014, Nature Genetics.
[22] K. Kinzler,et al. Cancer Genome Landscapes , 2013, Science.
[23] C. Sander,et al. Mutual exclusivity analysis identifies oncogenic network modules. , 2012, Genome research.
[24] Roded Sharan,et al. Simultaneous Identification of Multiple Driver Pathways in Cancer , 2013, PLoS Comput. Biol..
[25] Mark A van de Wiel,et al. BCL2L1 has a functional role in colorectal cancer and its protein expression is associated with chromosome 20q gain , 2012, The Journal of pathology.
[26] Kathleen Marchal,et al. SomInaClust: detection of cancer genes based on somatic mutation patterns of inactivation and clustering , 2015, BMC Bioinformatics.
[27] Irmtraud M. Meyer,et al. The clonal and mutational evolution spectrum of primary triple-negative breast cancers , 2012, Nature.
[28] Steven J. M. Jones,et al. Comprehensive molecular portraits of human breast tumors , 2012, Nature.
[29] Henning Hermjakob,et al. The Reactome pathway Knowledgebase , 2015, Nucleic acids research.
[30] David T. W. Jones,et al. Signatures of mutational processes in human cancer , 2013, Nature.
[31] Steven J. M. Jones,et al. Comprehensive molecular portraits of human breast tumours , 2013 .
[32] Jing Hu,et al. SIFT web server: predicting effects of amino acid substitutions on proteins , 2012, Nucleic Acids Res..
[33] P. Shannon,et al. Cytoscape: a software environment for integrated models of biomolecular interaction networks. , 2003, Genome research.
[34] Yang Liu,et al. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis , 2009, Nature Genetics.
[35] C. Sander,et al. Systematic identification of cancer driving signaling pathways based on mutual exclusivity of genomic alterations , 2014, Genome Biology.
[36] S. Gabriel,et al. Discovery and saturation analysis of cancer genes across 21 tumor types , 2014, Nature.
[37] C. Yeang,et al. Combinatorial patterns of somatic gene mutations in cancer , 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[38] Matthew B. Callaway,et al. MuSiC: Identifying mutational significance in cancer genomes , 2012, Genome research.