Integrated Analysis of CNV, Gene Expression and Disease State Data in Prostate Cancer
暂无分享,去创建一个
[1] Martin N. Davis,et al. Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome , 2020, Cancers.
[2] S. Cavallaro,et al. The contribution of CNVs to the most common aging-related neurodegenerative diseases , 2020, Aging Clinical and Experimental Research.
[3] Donghang Xu,et al. Copy number variation is highly correlated with differential gene expression: a pan-cancer study , 2019, BMC Medical Genetics.
[4] D. Gresham,et al. An evolving view of copy number variants , 2019, Current Genetics.
[5] Kyungsook Han,et al. Integration of Multi-Omics Data for Gene Regulatory Network Inference and Application to Breast Cancer , 2019, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[6] R. Vierkant,et al. Genome-wide Analysis of Common Copy Number Variation and Epithelial Ovarian Cancer Risk , 2019, Cancer Epidemiology, Biomarkers & Prevention.
[7] De-shuang Huang,et al. A Network-guided Association Mapping Approach from DNA Methylation to Disease , 2019, Scientific Reports.
[8] Yinyi Chen,et al. Identification of key candidate genes and biological pathways in bladder cancer , 2018, PeerJ.
[9] Yu-Dong Cai,et al. Identification of the copy number variant biomarkers for breast cancer subtypes , 2018, Molecular Genetics and Genomics.
[10] K. Hao,et al. EnsembleCNV: an ensemble machine learning algorithm to identify and genotype copy number variation using SNP array data , 2018, bioRxiv.
[11] James Y. Dai,et al. Identifying disease‐associated copy number variations by a doubly penalized regression model , 2018, Biometrics.
[12] Liang Fang,et al. Identification of Core Genes and Key Pathways via Integrated Analysis of Gene Expression and DNA Methylation Profiles in Bladder Cancer , 2018, Medical science monitor : international medical journal of experimental and clinical research.
[13] Adrian V. Lee,et al. An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics , 2018, Cell.
[14] Xiaodong Cui,et al. MeTDiff: A Novel Differential RNA Methylation Analysis for MeRIP-Seq Data , 2018, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[15] Yuan-ming Pan,et al. A Novel Method to Detect Early Colorectal Cancer Based on Chromosome Copy Number Variation in Plasma , 2018, Cellular Physiology and Biochemistry.
[16] S. Zhang,et al. S6K1 phosphorylation-dependent degradation of Mxi1 by β-Trcp ubiquitin ligase promotes Myc activation and radioresistance in lung cancer , 2018, Theranostics.
[17] De-Shuang Huang,et al. FAACOSE: A Fast Adaptive Ant Colony Optimization Algorithm for Detecting SNP Epistasis , 2017, Complex..
[18] Junfeng Xia,et al. Cancer Subtype Discovery Based on Integrative Model of Multigenomic Data , 2017, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[19] Xiaobo Zhou,et al. Nonconvex Penalty Based Low-Rank Representation and Sparse Regression for eQTL Mapping , 2017, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[20] Yufei Huang,et al. QNB: differential RNA methylation analysis for count-based small-sample sequencing data with a quad-negative binomial model , 2017, BMC Bioinformatics.
[21] Mary Goldman,et al. Abstract 2584: The UCSC Xena system for cancer genomics data visualization and interpretation , 2017 .
[22] C. Zheng,et al. LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network , 2016, BMC Bioinformatics.
[23] S. Cavallaro,et al. Copy number variability in Parkinson’s disease: assembling the puzzle through a systems biology approach , 2016, Human Genetics.
[24] K. Silverstein,et al. CNV-RF Is a Random Forest-Based Copy Number Variation Detection Method Using Next-Generation Sequencing. , 2016, The Journal of molecular diagnostics : JMD.
[25] Xiaodong Cui,et al. A novel algorithm for calling mRNA m6A peaks by modeling biological variances in MeRIP-seq data , 2016, Bioinform..
[26] Martín Abadi,et al. TensorFlow: Large-Scale Machine Learning on Heterogeneous Distributed Systems , 2016, ArXiv.
[27] J. Schleutker,et al. Germline copy number variation analysis in Finnish families with hereditary prostate cancer , 2016, The Prostate.
[28] M. Ladomery,et al. The oncogene ERG: a key factor in prostate cancer , 2016, Oncogene.
[29] J. Mesirov,et al. The Molecular Signatures Database Hallmark Gene Set Collection , 2015 .
[30] Patrick F. Sullivan,et al. A New Method for Detecting Associations with Rare Copy-Number Variants , 2015, PLoS genetics.
[31] De-shuang Huang,et al. Module Based Differential Coexpression Analysis Method for Type 2 Diabetes , 2015, BioMed research international.
[32] S. Mccarroll,et al. Complex and multi-allelic copy number variation in human disease , 2015, Briefings in functional genomics.
[33] J. Lupski. Structural variation mutagenesis of the human genome: Impact on disease and evolution , 2015, Environmental and molecular mutagenesis.
[34] A. Bahnassy,et al. Differentially expressed genes in metastatic advanced Egyptian bladder cancer. , 2015, Asian Pacific journal of cancer prevention : APJCP.
[35] J. R. MacDonald,et al. A copy number variation map of the human genome , 2015, Nature Reviews Genetics.
[36] K. Tomczak,et al. The Cancer Genome Atlas (TCGA): an immeasurable source of knowledge , 2015, Contemporary oncology.
[37] Lin Yuan,et al. Gene differential coexpression analysis based on biweight correlation and maximum clique , 2014, BMC Bioinformatics.
[38] C. Sotiriou,et al. Transfer of clinically relevant gene expression signatures in breast cancer: from Affymetrix microarray to Illumina RNA-Sequencing technology , 2014, BMC Genomics.
[39] Martin J. Aryee,et al. Epigenome-wide association studies without the need for cell-type composition , 2014, Nature Methods.
[40] Lars Feuk,et al. The Database of Genomic Variants: a curated collection of structural variation in the human genome , 2013, Nucleic Acids Res..
[41] Naoki Orii,et al. Wiki-Pi: A Web-Server of Annotated Human Protein-Protein Interactions to Aid in Discovery of Protein Function , 2012, PloS one.
[42] Chao Chen,et al. dbVar and DGVa: public archives for genomic structural variation , 2012, Nucleic Acids Res..
[43] Chunquan Li,et al. CNVD: Text mining‐based copy number variation in disease database , 2012, Human mutation.
[44] Ji-Hong Kim,et al. CNVRuler: a copy number variation-based case-control association analysis tool , 2012, Bioinform..
[45] Peter Langfelder,et al. Fast R Functions for Robust Correlations and Hierarchical Clustering. , 2012, Journal of statistical software.
[46] T. Furey,et al. Integrating genetic and gene expression evidence into genome-wide association analysis of gene sets. , 2011, Genome research.
[47] Chuhsing Kate Hsiao,et al. Integrated Analyses of Copy Number Variations and Gene Expression in Lung Adenocarcinoma , 2011, PloS one.
[48] 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.
[49] Michael DiCuccio,et al. Public data archives for genomic structural variation , 2010, Nature Genetics.
[50] Tsviya Olender,et al. GeneCards Version 3: the human gene integrator , 2010, Database J. Biol. Databases Curation.
[51] Manuel Corpas,et al. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. , 2009, American journal of human genetics.
[52] N. Meinshausen,et al. Stability selection , 2008, 0809.2932.
[53] Clifford A. Meyer,et al. Model-based Analysis of ChIP-Seq (MACS) , 2008, Genome Biology.
[54] Tomas W. Fitzgerald,et al. A robust statistical method for case-control association testing with copy number variation , 2008, Nature Genetics.
[55] R. Tibshirani,et al. Sparsity and smoothness via the fused lasso , 2005 .
[56] M. Daly,et al. PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes , 2003, Nature Genetics.
[57] M. Augustus,et al. PCGEM1, a prostate-specific gene, is overexpressed in prostate cancer. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[58] A. Jemal,et al. Global cancer statistics , 2011, CA: a cancer journal for clinicians.