DeepEnhancer: Predicting enhancers by convolutional neural networks
暂无分享,去创建一个
[1] J. Shendure,et al. A general framework for estimating the relative pathogenicity of human genetic variants , 2014, Nature Genetics.
[2] Razvan Pascanu,et al. Theano: new features and speed improvements , 2012, ArXiv.
[3] Manolis Kellis,et al. The NF-κB genomic landscape in lymphoblastoid B cells. , 2014, Cell reports.
[4] Morteza Mohammad Noori,et al. Enhanced Regulatory Sequence Prediction Using Gapped k-mer Features , 2014, PLoS Comput. Biol..
[5] Yanjun Qi,et al. Deep Motif: Visualizing Genomic Sequence Classifications , 2016, ArXiv.
[6] A. Visel,et al. Large-Scale Discovery of Enhancers from Human Heart Tissue , 2011, Nature Genetics.
[7] Jimmy Ba,et al. Adam: A Method for Stochastic Optimization , 2014, ICLR.
[8] Nitish Srivastava,et al. Dropout: a simple way to prevent neural networks from overfitting , 2014, J. Mach. Learn. Res..
[9] William Stafford Noble,et al. Quantifying similarity between motifs , 2007, Genome Biology.
[10] G. Bejerano,et al. Enhancers: five essential questions , 2013, Nature Reviews Genetics.
[11] B. Frey,et al. Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning , 2015, Nature Biotechnology.
[12] Cesare Furlanello,et al. A promoter-level mammalian expression atlas , 2015 .
[13] J. T. Kadonaga,et al. *To whom correspondence should be addressed. E- , 2022 .
[14] Manolis Kellis,et al. ChromHMM: automating chromatin-state discovery and characterization , 2012, Nature Methods.
[15] Shane C. Dillon,et al. The landscape of histone modifications across 1% of the human genome in five human cell lines. , 2007, Genome research.
[16] Hod Lipson,et al. Understanding Neural Networks Through Deep Visualization , 2015, ArXiv.
[17] Paul T. Groth,et al. The ENCODE (ENCyclopedia Of DNA Elements) Project , 2004, Science.
[18] Michael R. Green,et al. Transcriptional regulatory elements in the human genome. , 2006, Annual review of genomics and human genetics.
[19] David J. Arenillas,et al. JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles , 2015, Nucleic Acids Res..
[20] Michael A. Beer,et al. Discriminative prediction of mammalian enhancers from DNA sequence. , 2011, Genome research.
[21] Daniel Quang,et al. DanQ: a hybrid convolutional and recurrent deep neural network for quantifying the function of DNA sequences , 2015 .
[22] Sergey Ioffe,et al. Batch Normalization: Accelerating Deep Network Training by Reducing Internal Covariate Shift , 2015, ICML.
[23] T. Meehan,et al. An atlas of active enhancers across human cell types and tissues , 2014, Nature.
[24] Nathaniel D Heintzman,et al. Finding distal regulatory elements in the human genome. , 2009, Current opinion in genetics & development.
[25] Andrew Zisserman,et al. Deep Inside Convolutional Networks: Visualising Image Classification Models and Saliency Maps , 2013, ICLR.
[26] O. Troyanskaya,et al. Predicting effects of noncoding variants with deep learning–based sequence model , 2015, Nature Methods.
[27] E. Birney,et al. High-resolution genome-wide in vivo footprinting of diverse transcription factors in human cells. , 2011, Genome research.
[28] Xiaohui Xie,et al. DANN: a deep learning approach for annotating the pathogenicity of genetic variants , 2015, Bioinform..
[29] Mikael Bodén,et al. MEME Suite: tools for motif discovery and searching , 2009, Nucleic Acids Res..
[30] Geoffrey E. Hinton,et al. ImageNet classification with deep convolutional neural networks , 2012, Commun. ACM.
[31] David R. Kelley,et al. Basset: Learning the regulatory code of the accessible genome with deep convolutional neural networks , 2015 .