29 research outputs found

    Beating the Perils of Non-Convexity: Guaranteed Training of Neural Networks using Tensor Methods

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    Training neural networks is a challenging non-convex optimization problem, and backpropagation or gradient descent can get stuck in spurious local optima. We propose a novel algorithm based on tensor decomposition for guaranteed training of two-layer neural networks. We provide risk bounds for our proposed method, with a polynomial sample complexity in the relevant parameters, such as input dimension and number of neurons. While learning arbitrary target functions is NP-hard, we provide transparent conditions on the function and the input for learnability. Our training method is based on tensor decomposition, which provably converges to the global optimum, under a set of mild non-degeneracy conditions. It consists of simple embarrassingly parallel linear and multi-linear operations, and is competitive with standard stochastic gradient descent (SGD), in terms of computational complexity. Thus, we propose a computationally efficient method with guaranteed risk bounds for training neural networks with one hidden layer.Comment: The tensor decomposition analysis is expanded, and the analysis of ridge regression is added for recovering the parameters of last layer of neural networ

    Score Function Features for Discriminative Learning: Matrix and Tensor Framework

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    Feature learning forms the cornerstone for tackling challenging learning problems in domains such as speech, computer vision and natural language processing. In this paper, we consider a novel class of matrix and tensor-valued features, which can be pre-trained using unlabeled samples. We present efficient algorithms for extracting discriminative information, given these pre-trained features and labeled samples for any related task. Our class of features are based on higher-order score functions, which capture local variations in the probability density function of the input. We establish a theoretical framework to characterize the nature of discriminative information that can be extracted from score-function features, when used in conjunction with labeled samples. We employ efficient spectral decomposition algorithms (on matrices and tensors) for extracting discriminative components. The advantage of employing tensor-valued features is that we can extract richer discriminative information in the form of an overcomplete representations. Thus, we present a novel framework for employing generative models of the input for discriminative learning.Comment: 29 page

    Score Function Features for Discriminative Learning

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    Feature learning forms the cornerstone for tackling challenging learning problems in domains such as speech, computer vision and natural language processing. In this paper, we consider a novel class of matrix and tensor-valued features, which can be pre-trained using unlabeled samples. We present efficient algorithms for extracting discriminative information, given these pre-trained features and labeled samples for any related task. Our class of features are based on higher-order score functions, which capture local variations in the probability density function of the input. We establish a theoretical framework to characterize the nature of discriminative information that can be extracted from score-function features, when used in conjunction with labeled samples. We employ efficient spectral decomposition algorithms (on matrices and tensors) for extracting discriminative components. The advantage of employing tensor-valued features is that we can extract richer discriminative information in the form of an overcomplete representations. Thus, we present a novel framework for employing generative models of the input for discriminative learning

    Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication

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    Misalignments of low-copy repeats (LCRs) located in chromosome 22, particularly band 22q11.2, predispose to rearrangements. A variety of phenotypic features are associated with 22q11.2 microduplication syndrome which makes it challenging for the genetic counselors to recommend appropriate genetic assessment and counseling for the patients. In this study, multiplex ligation probe dependent amplification (MLPA) analysis was performed on 378 patients with cleft lip and/or palate to characterize rearrangements in patients suspected of 22q11.2 microduplication and microdeletion syndromes. Of 378 cases, 15 were diagnosed with a microdeletion with various sizes and 3 with duplications. For the first time in this study an atypical 0.6 Mb duplication is reported. Illustration of the phenotypes associated with the microduplications increases the knowledge of phenotypes reported in the literature

    Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome

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    AbstractObjectivesRett syndrome is an X linked dominant neurodevelopmental disorder which almost exclusively affects females. The syndrome is usually caused by mutations in MECP2 gene, which is a nuclear protein that selectively binds CpG dinucleotides in the genome.Materials & MethodsTo provide further insights into the distribution of mutations in MECP2 gene, we investigated 24 females with clinical characters of Rett syndrome referred to Alzahra University Hospital in Isfahan, Iran during 2015-2017. We sequenced the entire MECP2 coding region and splice sites for detection of point mutations in this gene. Freely available programs including JALVIEW, SIFT, and PolyPhen were used to find out the damaging effects of unknown mutations.ResultsDirect sequencing revealed MECP2 mutations in 13 of the 24 patients. We identified in 13 patients, 10 different mutations in MECP2 gene. Three of these mutations have not been reported elsewhere and are most likely pathogenic.ConclusionDefects in MECP2 gene play an important role in pathogenesis of Rett syndrome. Mutations in MECP2 gene can be found in the majority of Iranian RTT patients. We failed to identify mutations in MECP2 gene in 46% of our patients. For these patients, further molecular analysis might be necessary
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