Visualization of non-metric relationships by adaptive learning multiple maps t-SNE regularization
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Xianchao Zhu | Xianjun Shen | Xingpeng Jiang | Xiaohua Hu | Tingting He | Li Gao | Xiaohua Hu | Tingting He | Xingpeng Jiang | Xianjun Shen | Xianchao Zhu | Li Gao
[1] Razvan Pascanu,et al. Advances in optimizing recurrent networks , 2012, 2013 IEEE International Conference on Acoustics, Speech and Signal Processing.
[2] Jan Freudenberg,et al. A similarity-based method for genome-wide prediction of disease-relevant human genes , 2002, ECCB.
[3] Krishnakumar Balasubramanian,et al. Dimensionality Reduction for Text using Domain Knowledge , 2010, COLING.
[4] Xingpeng Jiang,et al. Visualization of genetic disease-phenotype similarities by multiple maps t-SNE with Laplacian regularization , 2014, BMC Medical Genomics.
[5] Ruth Nussinov,et al. Structure and dynamics of molecular networks: A novel paradigm of drug discovery. A comprehensive review , 2012, Pharmacology & therapeutics.
[6] Yurii Nesterov,et al. Lectures on Convex Optimization , 2018 .
[7] Geoffrey E. Hinton,et al. Training Recurrent Neural Networks , 2013 .
[8] Xianchao Zhu,et al. Visualization of disease relationships by multiple maps t-SNE regularization based on Nesterov accelerated gradient , 2017, 2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).
[9] Qiang Feng,et al. A metagenome-wide association study of gut microbiota in type 2 diabetes , 2012, Nature.
[10] Susumu Goto,et al. The commonality of protein interaction networks determined in neurodegenerative disorders (NDDs) , 2007, Bioinform..
[11] S. Mundlos,et al. A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN. , 2007, American journal of human genetics.
[12] G. Vriend,et al. A text-mining analysis of the human phenome , 2006, European Journal of Human Genetics.
[13] Jacob Sosna,et al. P35S mutation in the NOG gene associated with Teunissen-Cremers syndrome and features of multiple NOG joint-fusion syndromes. , 2008, European journal of medical genetics.
[14] Geoffrey E. Hinton,et al. Visualizing Data using t-SNE , 2008 .
[15] T. Jiang,et al. Modularity in the genetic disease‐phenotype network , 2008, FEBS letters.
[16] Michael I. Jordan,et al. DiscLDA: Discriminative Learning for Dimensionality Reduction and Classification , 2008, NIPS.
[17] Peilin Jia,et al. Multi-Dimensional Prioritization of Dental Caries Candidate Genes and Its Enriched Dense Network Modules , 2013, PloS one.
[18] H. Brunner,et al. From syndrome families to functional genomics , 2004, Nature Reviews Genetics.
[19] Geoffrey E. Hinton,et al. Visualizing non-metric similarities in multiple maps , 2011, Machine Learning.
[20] A. Barabasi,et al. Human disease classification in the postgenomic era: A complex systems approach to human pathobiology , 2007, Molecular systems biology.
[21] D. Valle,et al. Online Mendelian Inheritance In Man (OMIM) , 2000, Human mutation.
[22] Volkan Cevher,et al. Stochastic Spectral Descent for Restricted Boltzmann Machines , 2015, AISTATS.
[23] A. Barabasi,et al. A Protein–Protein Interaction Network for Human Inherited Ataxias and Disorders of Purkinje Cell Degeneration , 2006, Cell.
[24] B. Snel,et al. Predicting disease genes using protein–protein interactions , 2006, Journal of Medical Genetics.