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Publications
SkillQG: Learning to Generate Question for Reading Comprehension Assessment
Deep learning-based algorithms have been very successful in skeleton-based human activity recognition. Skeleton data contains 2-D or 3-D coo… (see more)rdinates of human body joints. The main focus of most of the existing skeleton-based activity recognition methods is on designing new deep architectures to learn discriminative features, where all body joints are considered equally important in recognition. However, the importance of joints varies as an activity proceeds within a video and across different activities. In this work, we hypothesize that selecting relevant joints, prior to recognition, can enhance performance of the existing deep learning-based recognition models. We propose a spatial hard attention finding method that aims to remove the uninformative and/or misleading joints at each frame. We formulate the joint selection problem as a Markov decision process and employ deep reinforcement learning to train the proposed spatial-attention-aware agent. No extra labels are needed for the agent’s training. The agent takes a sequence of features extracted from skeleton video as input and outputs a sequence of probabilities for joints. The proposed method can be considered as a general framework that can be integrated with the existing skeleton-based activity recognition methods for performance improvement purposes. We obtain very competitive activity recognition results on three commonly used human activity recognition datasets.
2023-07-01
IEEE Transactions on Systems, Man, and Cybernetics: Systems (published)
Abstract Motivation Accurately assessing contacts between DNA fragments inside the nucleus with Hi-C experiment is crucial for understanding… (see more) the role of 3D genome organization in gene regulation. This challenging task is due in part to the high sequencing depth of Hi-C libraries required to support high-resolution analyses. Most existing Hi-C data are collected with limited sequencing coverage, leading to poor chromatin interaction frequency estimation. Current computational approaches to enhance Hi-C signals focus on the analysis of individual Hi-C datasets of interest, without taking advantage of the facts that (i) several hundred Hi-C contact maps are publicly available and (ii) the vast majority of local spatial organizations are conserved across multiple cell types. Results Here, we present RefHiC-SR, an attention-based deep learning framework that uses a reference panel of Hi-C datasets to facilitate the enhancement of Hi-C data resolution of a given study sample. We compare RefHiC-SR against tools that do not use reference samples and find that RefHiC-SR outperforms other programs across different cell types, and sequencing depths. It also enables high-accuracy mapping of structures such as loops and topologically associating domains. Availability and implementation https://github.com/BlanchetteLab/RefHiC.
Disentanglement aims to recover meaningful latent ground-truth factors from the observed distribution solely, and is formalized through the … (see more)theory of identifiability. The identifiability of independent latent factors is proven to be impossible in the unsupervised i.i.d. setting under a general nonlinear map from factors to observations. In this work, however, we demonstrate that it is possible to recover quantized latent factors under a generic nonlinear diffeomorphism. We only assume that the latent factors have independent discontinuities in their density, without requiring the factors to be statistically independent. We introduce this novel form of identifiability, termed quantized factor identifiability, and provide a comprehensive proof of the recovery of the quantized factors.
Genomic (DNA) sequences encode an enormous amount of information for gene regulation and protein synthesis. Similar to natural language mode… (see more)ls, researchers have proposed foundation models in genomics to learn generalizable features from unlabeled genome data that can then be fine-tuned for downstream tasks such as identifying regulatory elements. Due to the quadratic scaling of attention, previous Transformer-based genomic models have used 512 to 4k tokens as context (0.001% of the human genome), significantly limiting the modeling of long-range interactions in DNA. In addition, these methods rely on toke
Genomic (DNA) sequences encode an enormous amount of information for gene regulation and protein synthesis. Similar to natural language mode… (see more)ls, researchers have proposed foundation models in genomics to learn generalizable features from unlabeled genome data that can then be fine-tuned for downstream tasks such as identifying regulatory elements. Due to the quadratic scaling of attention, previous Transformer-based genomic models have used 512 to 4k tokens as context (0.001% of the human genome), significantly limiting the modeling of long-range interactions in DNA. In addition, these methods rely on toke
Genomic (DNA) sequences encode an enormous amount of information for gene regulation and protein synthesis. Similar to natural language mode… (see more)ls, researchers have proposed foundation models in genomics to learn generalizable features from unlabeled genome data that can then be fine-tuned for downstream tasks such as identifying regulatory elements. Due to the quadratic scaling of attention, previous Transformer-based genomic models have used 512 to 4k tokens as context (0.001% of the human genome), significantly limiting the modeling of long-range interactions in DNA. In addition, these methods rely on toke
Genomic (DNA) sequences encode an enormous amount of information for gene regulation and protein synthesis. Similar to natural language mode… (see more)ls, researchers have proposed foundation models in genomics to learn generalizable features from unlabeled genome data that can then be fine-tuned for downstream tasks such as identifying regulatory elements. Due to the quadratic scaling of attention, previous Transformer-based genomic models have used 512 to 4k tokens as context (0.001% of the human genome), significantly limiting the modeling of long-range interactions in DNA. In addition, these methods rely on toke
