Inferring subgroup-specific driver genes from heterogeneous cancer samples via subspace learning with subgroup indication
暂无分享,去创建一个
Xuelong Li | Qinghua Huang | Ao Li | Xiguo Yuan | Jianing Xi | Minghui Wang | Qinghua Huang | Ao Li | Minghui Wang | Xiguo Yuan | Jianing Xi | Xuelong Li
[1] K. Tomczak,et al. The Cancer Genome Atlas (TCGA): an immeasurable source of knowledge , 2015, Contemporary oncology.
[2] N. Rosenfeld,et al. The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes , 2016, Nature Communications.
[3] Gary D Bader,et al. International network of cancer genome projects , 2010, Nature.
[4] David Tamborero,et al. OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes , 2013, Bioinform..
[5] Thomas S. Huang,et al. Graph Regularized Nonnegative Matrix Factorization for Data Representation. , 2011, IEEE transactions on pattern analysis and machine intelligence.
[6] Steven A. Roberts,et al. Mutational heterogeneity in cancer and the search for new cancer genes , 2014 .
[7] Tieniu Tan,et al. Joint Feature Selection and Subspace Learning for Cross-Modal Retrieval , 2016, IEEE Transactions on Pattern Analysis and Machine Intelligence.
[8] Jin Gu,et al. Evaluating the molecule-based prediction of clinical drug responses in cancer , 2016, Bioinform..
[9] P. Sooriakumaran,et al. Tumour heterogeneity poses a significant challenge to cancer biomarker research , 2017, British Journal of Cancer.
[10] Steven J. M. Jones,et al. Comprehensive molecular characterization of urothelial bladder carcinoma , 2014, Nature.
[11] Aapo Hyvärinen,et al. Independent component analysis: recent advances , 2013, Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.
[12] T. Mukohara,et al. PI3K mutations in breast cancer: prognostic and therapeutic implications , 2015, Breast cancer.
[13] Shihua Zhang,et al. Tumor characterization and stratification by integrated molecular profiles reveals essential pan-cancer features , 2015, BMC Genomics.
[14] S. Ganesan,et al. Looking beyond drivers and passengers in cancer genome sequencing data. , 2016, Annals of oncology : official journal of the European Society for Medical Oncology.
[15] K. Kinzler,et al. Evaluating the evaluation of cancer driver genes , 2016, Proceedings of the National Academy of Sciences.
[16] Pablo Tamayo,et al. Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[17] Emmanuel J. Candès,et al. Decoding by linear programming , 2005, IEEE Transactions on Information Theory.
[18] C. Cole,et al. The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers , 2018, Nature Reviews Cancer.
[19] Ao Li,et al. CLImAT: accurate detection of copy number alteration and loss of heterozygosity in impure and aneuploid tumor samples using whole-genome sequencing data , 2014, Bioinform..
[20] Juan Liu,et al. Pattern fusion analysis by adaptive alignment of multiple heterogeneous omics data , 2017, Bioinform..
[21] S. Gabriel,et al. Advances in understanding cancer genomes through second-generation sequencing , 2010, Nature Reviews Genetics.
[22] Yili Yin,et al. p53 stability and activity is regulated by Mdm2-mediated induction of alternative p53 translation products , 2002, Nature Cell Biology.
[23] A. Shaw,et al. Tumour heterogeneity and resistance to cancer therapies , 2018, Nature Reviews Clinical Oncology.
[24] Benjamin E. Gross,et al. Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal , 2013, Science Signaling.
[25] Shihua Zhang,et al. Discovery of cancer common and specific driver gene sets , 2016, Nucleic acids research.
[26] Yi Pan,et al. SinNLRR: a robust subspace clustering method for cell type detection by non-negative and low-rank representation , 2019, Bioinform..
[27] Leyla Isik,et al. Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. , 2009, Cancer research.
[28] Vladik Kreinovich,et al. Why l1 Is a Good Approximation to l0: A Geometric Explanation , 2013 .
[29] K. Kinzler,et al. Cancer Genome Landscapes , 2013, Science.
[30] Yang Zheng,et al. Capsule Network Based Modeling of Multi-omics Data for Discovery of Breast Cancer-Related Genes , 2020, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[31] Steven J. M. Jones,et al. Comprehensive Characterization of Cancer Driver Genes and Mutations , 2018, Cell.
[32] Joshua M. Stuart,et al. The Cancer Genome Atlas Pan-Cancer analysis project , 2013, Nature Genetics.
[33] Steven J. M. Jones,et al. Comprehensive molecular portraits of human breast tumors , 2012, Nature.
[34] Jing Liu,et al. Robust Structured Subspace Learning for Data Representation , 2015, IEEE Transactions on Pattern Analysis and Machine Intelligence.
[35] Na-Na Guan,et al. Predicting miRNA‐disease association based on inductive matrix completion , 2018, Bioinform..
[36] Guojun Li,et al. MaxMIF: A New Method for Identifying Cancer Driver Genes through Effective Data Integration , 2018, Advanced science.
[37] Ash A. Alizadeh,et al. Toward understanding and exploiting tumor heterogeneity , 2015, Nature Medicine.
[38] A. Jemal,et al. Cancer statistics, 2019 , 2019, CA: a cancer journal for clinicians.
[39] Dacheng Tao,et al. Double Shrinking Sparse Dimension Reduction , 2013, IEEE Transactions on Image Processing.
[40] Xiaobo Zhou,et al. A novel missense-mutation-related feature extraction scheme for 'driver' mutation identification , 2012, Bioinform..
[41] Ao Li,et al. A novel approach for drug response prediction in cancer cell lines via network representation learning , 2018, Bioinform..
[42] Jorge Cadima,et al. Principal component analysis: a review and recent developments , 2016, Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.
[43] Zhen Cao,et al. An Integrative Framework for Combining Sequence and Epigenomic Data to Predict Transcription Factor Binding Sites Using Deep Learning , 2019, IEEE/ACM Transactions on Computational Biology and Bioinformatics.