Abstract:
A system for electronic message classification and delivery using a neural network architecture includes one or more computing devices associated with one or more users, and at least one computer processing system in communication with one or more computing devices over at least one network. The at least one computer processing system includes at least one processor operatively coupled to a memory device and configured to execute program code stored on the memory device to receive one or more inputs associated with one or more e-mails corresponding to the one or more users across the at least one network, classify the one or more e-mails by performing natural language processing based on one or more sets of filters conditioned on respective ones of the one or more inputs, and permit the one or more users access to the one or more classified e-mails via the one or more computing devices.
Abstract:
Mobile phones and methods for mobile phone failure prediction include receiving respective log files from one or more mobile phone components, including at least one user application. The log files have heterogeneous formats. A likelihood of failure of one or more mobile phone components is determined based on the received log files by clustering the plurality of log files according to structural log patterns and determining feature representations of the log files based on the log clusters. A user is alerted to a potential failure if the likelihood of component failure exceeds a first threshold. An automatic system control action is performed if the likelihood of component failure exceeds a second threshold.
Abstract:
An optimization-driven sparse learning framework is disclosed to identify discriminative system components among system input features that are essential for system output prediction. In biomarker discovery, to handle the combinatorial interactions among gene or protein expression measurements for identifying interaction complexes and disease biomarkers, the system uses both single input features and high-order input feature interactions.
Abstract:
Methods and systems for training a neural network include pre-training a bi-linear, tensor-based network, separately pre-training an auto-encoder, and training the bi-linear, tensor-based network and auto-encoder jointly. Pre-training the bi-linear, tensor-based network includes calculating high-order interactions between an input and a transformation to determine a preliminary network output and minimizing a loss function to pre-train network parameters. Pre-training the auto-encoder includes calculating high-order interactions of a corrupted real network output, determining an auto-encoder output using high-order interactions of the corrupted real network output, and minimizing a loss function to pre-train auto-encoder parameters.
Abstract:
Systems and method are disclosed for determining complex interactions among system inputs by using semi-Restricted Boltzmann Machines (RBMs) with factorized gated interactions of different orders to model complex interactions among system inputs; applying semi-RBMs to train a deep neural network with high-order within-layer interactions for learning a distance metric and a feature mapping; and tuning the deep neural network by minimizing margin violations between positive query document pairs and corresponding negative pairs.
Abstract:
Systems and methods include predicting a first action step and a last action step based on an initial visual observation and a goal visual state and retrieving multiple procedural plans from a procedural knowledge graph (PKG), trained using a set of training instructional videos, which start with the first action step and end with the last action step. A procedure plan is generated using the retrieved multiple procedural plans. An instructional video is generated based on the procedure plan.
Abstract:
A method for learning disentangled representations of videos is presented. The method includes feeding each frame of video data into an encoder to produce a sequence of visual features, passing the sequence of visual features through a deep convolutional network to obtain a posterior of a dynamic latent variable and a posterior of a static latent variable, sampling static and dynamic representations from the posterior of the static latent variable and the posterior of the dynamic latent variable, respectively, concatenating the static and dynamic representations to be fed into a decoder to generate reconstructed sequences, and applying three regularizers to the dynamic and static latent variables to trigger representation disentanglement. To facilitate the disentangled sequential representation learning, orthogonal factorization in generative adversarial network (GAN) latent space is leveraged to pre-train a generator as a decoder in the method.
Abstract:
A method for implementing deep reinforcement learning with T-cell receptor (TCR) mutation policies to generate binding TCRs recognizing target peptides for immunotherapy is presented. The method includes extracting peptides to identify a virus or tumor cells, collecting a library of TCRs from target patients, predicting, by a deep neural network, interaction scores between the extracted peptides and the TCRs from the target patients, developing a deep reinforcement learning (DRL) framework with TCR mutation policies to generate TCRs with maximum binding scores, defining reward functions based on a reconstruction-based score and a density estimation-based score, randomly sampling batches of TCRs and following a policy network to mutate the TCRs, outputting mutated TCRs, and ranking the outputted TCRs to utilize top-ranked TCR candidates to target the virus or the tumor cells for immunotherapy.
Abstract:
A method for implementing deep reinforcement learning with T-cell receptor (TCR) mutation policies to generate binding TCRs recognizing target peptides for immunotherapy is presented. The method includes extracting peptides to identify a virus or tumor cells, collecting a library of TCRs from target patients, predicting, by a deep neural network, interaction scores between the extracted peptides and the TCRs from the target patients, developing a deep reinforcement learning (DRL) framework with TCR mutation policies to generate TCRs with maximum binding scores, defining reward functions based on a reconstruction-based score and a density estimation-based score, randomly sampling batches of TCRs and following a policy network to mutate the TCRs, outputting mutated TCRs, and ranking the outputted TCRs to utilize top-ranked TCR candidates to target the virus or the tumor cells for immunotherapy.
Abstract:
A computer-implemented method is provided for generating new binding peptides to Major Histocompatibility Complex (MHC) proteins. The method includes training, by a processor device, a Generative Adversarial Network GAN having a generator and a discriminator only on a set of binding peptide sequences given training data comprising the set of binding peptide sequences and a set of non-binding peptide sequences. A GAN training objective includes the discriminator being iteratively updated to distinguish generated peptide sequences from sampled binding peptide sequences as fake or real and the generator being iteratively updated to fool the discriminator. The training includes optimizing the GAN training objective while learning two projection vectors for a binding class with two cross-entropy losses. A first loss discriminating binding peptide sequences in the training data from non-binding peptide sequences in the training data. A second loss discriminating generated binding peptide sequences from non-binding peptide sequences in the training data.