Oncogenomic portals for the visualization and analysis of genome-wide cancer data
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Luiza Handschuh | Marzena Wojciechowska | Marek Figlerowicz | M. Figlerowicz | P. Kozłowski | A. Zmienko | Katarzyna Klonowska | Karol Czubak | Agnieszka Zmienko | Hanna Dams-Kozlowska | Piotr Kozlowski | L. Handschuh | M. Wojciechowska | H. Dams-Kozlowska | K. Klonowska | Karol Czubak
[1] Kevin B. Jones,et al. miR-27a and miR-27a* contribute to metastatic properties of osteosarcoma cells , 2015, Oncotarget.
[2] M. Stratton,et al. COSMIC 2005 , 2006, British Journal of Cancer.
[3] Nuria Lopez-Bigas,et al. IntOGen: integration and data mining of multidimensional oncogenomic data , 2010, Nature Methods.
[4] Zhi Chen,et al. CaSNP: a database for interrogating copy number alterations of cancer genome from SNP array data , 2010, Nucleic Acids Res..
[5] David Haussler,et al. Inference of patient-specific pathway activities from multi-dimensional cancer genomics data using PARADIGM , 2010, Bioinform..
[6] Gary D Bader,et al. International network of cancer genome projects , 2010, Nature.
[7] Xuefei Shi,et al. The long non-coding RNA HNF1A-AS1 regulates proliferation and metastasis in lung adenocarcinoma , 2015, Oncotarget.
[8] Mingming Jia,et al. COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer , 2010, Nucleic Acids Res..
[9] P. Fisher,et al. Analysis of Global Changes in Gene Expression Induced by Human Polynucleotide Phosphorylase (hPNPaseold‐35) , 2014, Journal of cellular physiology.
[10] K. Gulukota,et al. Direct observation of genomic heterogeneity through local haplotyping analysis , 2014, BMC Genomics.
[11] Michael P. Schroeder,et al. IntOGen-mutations identifies cancer drivers across tumor types , 2013, Nature Methods.
[12] Modesto Orozco,et al. Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads , 2014, Nature Biotechnology.
[13] Curtis R. Pickering,et al. Mutational Landscape of Aggressive Cutaneous Squamous Cell Carcinoma , 2014, Clinical Cancer Research.
[14] P. Dessen,et al. Genome-Wide High-Resolution aCGH Analysis of Gestational Choriocarcinomas , 2012, PloS one.
[15] Pietro Liò,et al. The BioMart community portal: an innovative alternative to large, centralized data repositories , 2015, Nucleic Acids Res..
[16] Chi-Hung Lin,et al. Single Nucleotide Polymorphisms Associated with Colorectal Cancer Susceptibility and Loss of Heterozygosity in a Taiwanese Population , 2014, PloS one.
[17] M. Stratton,et al. The cancer genome , 2009, Nature.
[18] Martijn A. Huynen,et al. Predicting Human Genetic Interactions from Cancer Genome Evolution , 2015, PloS one.
[19] R. Mathur,et al. Inhibition of Methyltransferases Accelerates Degradation of cFLIP and Sensitizes B-Cell Lymphoma Cells to TRAIL-Induced Apoptosis , 2015, PloS one.
[20] David Tamborero,et al. OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes , 2013, Bioinform..
[21] M. Morello,et al. Bioinformatics analysis of the serine and glycine pathway in cancer cells , 2014, Oncotarget.
[22] W. Hahn,et al. Integrative Analysis of 1q23.3 Copy-Number Gain in Metastatic Urothelial Carcinoma , 2014, Clinical Cancer Research.
[23] N. A. Temiz,et al. APOBEC3B is an enzymatic source of mutation in breast cancer , 2013, Nature.
[24] N. Borcherding,et al. Bone Marrow Stromal Antigen 2 (BST-2) DNA Is Demethylated in Breast Tumors and Breast Cancer Cells , 2015, PloS one.
[25] X J Li,et al. MicroRNA-34a: a potential therapeutic target in human cancer , 2014, Cell Death and Disease.
[26] Rui Zhang,et al. An integrated approach to reveal miRNAs’ impacts on the functional consequence of copy number alterations in cancer , 2015, Scientific Reports.
[27] B. Reva,et al. MAP2K1 (MEK1) Mutations Define a Distinct Subset of Lung Adenocarcinoma Associated with Smoking , 2014, Clinical Cancer Research.
[28] D. Dickson. Wellcome funds cancer database , 1999, Nature.
[29] Circulating miR-200c and miR-141 and outcomes in patients with breast cancer , 2015, BMC Cancer.
[30] Benjamin E. Gross,et al. Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal , 2013, Science Signaling.
[31] C. Croce,et al. FHIT Suppresses Epithelial-Mesenchymal Transition (EMT) and Metastasis in Lung Cancer through Modulation of MicroRNAs , 2014, PLoS genetics.
[32] M. Figlerowicz,et al. High copy number variation of cancer-related microRNA genes and frequent amplification of DICER1 and DROSHA in lung cancer , 2015, Oncotarget.
[33] Michael P. Schroeder,et al. In silico prescription of anticancer drugs to cohorts of 28 tumor types reveals targeting opportunities. , 2015, Cancer cell.
[34] Joshua M. Korn,et al. Comprehensive genomic characterization defines human glioblastoma genes and core pathways , 2008, Nature.
[35] Mary Goldman,et al. The UCSC Cancer Genomics Browser: update 2015 , 2014, Nucleic Acids Res..
[36] A. Antonov,et al. Characterization of novel markers of senescence and their prognostic potential in cancer , 2014, Cell Death and Disease.
[37] David Tamborero,et al. OncodriveROLE classifies cancer driver genes in loss of function and activating mode of action , 2014, Bioinform..
[38] Benjamin E. Gross,et al. The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. , 2012, Cancer discovery.
[39] Hong Chang,et al. Multiple myeloma acquires resistance to EGFR inhibitor via induction of pentose phosphate pathway , 2015, Scientific Reports.
[40] M. Stratton,et al. The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website , 2004, British Journal of Cancer.
[41] D. Haussler,et al. Exploring TCGA Pan-Cancer Data at the UCSC Cancer Genomics Browser , 2013, Scientific Reports.
[42] M. Kahn,et al. Genomic and Functional Analysis of the E3 Ligase PARK2 in Glioma. , 2015, Cancer research.
[43] Syed Haider,et al. International Cancer Genome Consortium Data Portal—a one-stop shop for cancer genomics data , 2011, Database J. Biol. Databases Curation.
[44] Jian Yu,et al. Fibulin-3 suppresses Wnt/β-catenin signaling and lung cancer invasion. , 2014, Carcinogenesis.
[45] L. Chin,et al. Making sense of cancer genomic data. , 2011, Genes & development.
[46] R. Knight,et al. MIRUMIR: an online tool to test microRNAs as biomarkers to predict survival in cancer using multiple clinical data sets , 2012, Cell Death and Differentiation.
[47] Alexey V. Antonov,et al. BioProfiling.de: analytical web portal for high-throughput cell biology , 2011, Nucleic Acids Res..
[48] Zihua Zeng,et al. OLA1 regulates protein synthesis and integrated stress response by inhibiting eIF2 ternary complex formation , 2015, Scientific Reports.
[49] Marco Beccuti,et al. The molecular landscape of colorectal cancer cell lines unveils clinically actionable kinase targets , 2015, Nature Communications.
[50] K. Dahlman-Wright,et al. Genome-wide profiling of AP-1-regulated transcription provides insights into the invasiveness of triple-negative breast cancer. , 2014, Cancer research.
[51] S. Powers. Cooperation between MYC and companion 8q genes in hepatocarcinogenesis , 2015, Hepatology.
[52] Marissa A. LeBlanc,et al. Germline Mutations in MAP3K6 Are Associated with Familial Gastric Cancer , 2014, PLoS genetics.
[53] Gary D Bader,et al. Comprehensive identification of mutational cancer driver genes across 12 tumor types , 2013, Scientific Reports.
[54] B. Schittek,et al. Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis , 2014, Molecular Cancer.
[55] Cheng Liang,et al. Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach , 2014, Nucleic acids research.
[56] S A Forbes,et al. The Catalogue of Somatic Mutations in Cancer (COSMIC) , 2008, Current protocols in human genetics.
[57] Derek Y. Chiang,et al. The landscape of somatic copy-number alteration across human cancers , 2010, Nature.
[58] T. Barrette,et al. ONCOMINE: a cancer microarray database and integrated data-mining platform. , 2004, Neoplasia.
[59] D. Hanahan,et al. Hallmarks of Cancer: The Next Generation , 2011, Cell.
[60] Jie Zhang,et al. Exome sequencing identifies frequent mutation of MLL2 in non–small cell lung carcinoma from Chinese patients , 2014, Scientific Reports.
[61] Esti Yeger-Lotem,et al. Cancer Evolution Is Associated with Pervasive Positive Selection on Globally Expressed Genes , 2014, PLoS genetics.
[62] Ting Wang,et al. The UCSC Cancer Genomics Browser , 2009, Nature Methods.
[63] R A Knight,et al. DRUGSURV: a resource for repositioning of approved and experimental drugs in oncology based on patient survival information , 2014, Cell Death and Disease.
[64] W. Curran,et al. Identification of a tumor-suppressive human-specific microRNA within the FHIT tumor-suppressor gene. , 2014, Cancer research.
[65] Thomas M. Keane,et al. POT1 loss-of-function variants predispose to familial melanoma , 2014, Nature Genetics.
[66] Mary Goldman,et al. The UCSC Cancer Genomics Browser: update 2015 , 2014, Nucleic Acids Res..
[67] Michael A. Davies,et al. Pathways and therapeutic targets in melanoma , 2014, Oncotarget.
[68] Nuria Lopez-Bigas,et al. Visualizing multidimensional cancer genomics data , 2013, Genome Medicine.
[69] A. Gonzalez-Perez,et al. Functional impact bias reveals cancer drivers , 2012, Nucleic acids research.
[70] Steven A. Roberts,et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes , 2013 .
[71] R A Knight,et al. PPISURV: a novel bioinformatics tool for uncovering the hidden role of specific genes in cancer survival outcome , 2014, Oncogene.
[72] I. Varela,et al. Recurrent chromosomal gains and heterogeneous driver mutations characterise papillary renal cancer evolution , 2015, Nature Communications.
[73] Susan G. Hilsenbeck,et al. Recurrent ESR1-CCDC170 rearrangements in an aggressive subset of estrogen-receptor positive breast cancers , 2014, Nature Communications.
[74] A. Morokoff,et al. Coexpression analysis of CD133 and CD44 identifies Proneural and Mesenchymal subtypes of glioblastoma multiforme , 2015, Oncotarget.
[75] Circulating tumor cells in hepatocellular carcinoma: a pilot study of detection, enumeration, and next-generation sequencing in cases and controls , 2015, BMC Cancer.
[76] Yan Guo,et al. Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk , 2014, Nature Genetics.
[77] A. Antonov,et al. DNA damage modulates interactions between microRNAs and the 26S proteasome , 2014, Oncotarget.