Exploration of visual prompt in Grounded pre-trained open-set detection

Text prompts are crucial for generalizing pre-trained open-set object detection models to new categories. However, current methods for text prompts are limited as they require manual feedback when generalizing to new categories, which restricts their ability to model complex scenes, often leading to incorrect detection results. To address this limitation, we propose a novel visual prompt method that learns new category knowledge from a few labeled images, which generalizes the pre-trained detection model to the new category. To allow visual prompts to represent new categories adequately, we propose a statistical-based prompt construction module that is not limited by predefined vocabulary lengths, thus allowing more vectors to be used when representing categories. We further utilize the category dictionaries in the pre-training dataset to design task-specific similarity dictionaries, which make visual prompts more discriminative. We evaluate the method on the ODinW dataset and show that it outperforms existing prompt learning methods and performs more consistently in combinatorial inference.

Machine Learning Study of the Extended Drug-target Interaction Network informed by Pain Related Voltage-Gated Sodium Channels

Pain is a significant global health issue, and the current treatment options for pain management have limitations in terms of effectiveness, side effects, and potential for addiction. There is a pressing need for improved pain treatments and the development of new drugs. Voltage-gated sodium channels, particularly Nav1.3, Nav1.7, Nav1.8, and Nav1.9, play a crucial role in neuronal excitability and are predominantly expressed in the peripheral nervous system. Targeting these channels may provide a means to treat pain while minimizing central and cardiac adverse effects. In this study, we construct protein-protein interaction (PPI) networks based on pain-related sodium channels and develop a corresponding drug-target interaction (DTI) network to identify potential lead compounds for pain management. To ensure reliable machine learning predictions, we carefully select 111 inhibitor datasets from a pool of over 1,000 targets in the PPI network. We employ three distinct machine learning algorithms combined with advanced natural language processing (NLP)-based embeddings, specifically pre-trained transformer and autoencoder representations. Through a systematic screening process, we evaluate the side effects and repurposing potential of over 150,000 drug candidates targeting Nav1.7 and Nav1.8 sodium channels. Additionally, we assess the ADMET (absorption, distribution, metabolism, excretion, and toxicity) properties of these candidates to identify leads with near-optimal characteristics. Our strategy provides an innovative platform for the pharmacological development of pain treatments, offering the potential for improved efficacy and reduced side effects.

Neural Weight Search for Scalable Task Incremental Learning

Task incremental learning aims to enable a system to maintain its performance on previously learned tasks while learning new tasks, solving the problem of catastrophic forgetting. One promising approach is to build an individual network or sub-network for future tasks. However, this leads to an ever-growing memory due to saving extra weights for new tasks and how to address this issue has remained an open problem in task incremental learning. In this paper, we introduce a novel Neural Weight Search technique that designs a fixed search space where the optimal combinations of frozen weights can be searched to build new models for novel tasks in an end-to-end manner, resulting in scalable and controllable memory growth. Extensive experiments on two benchmarks, i.e., Split-CIFAR-100 and CUB-to-Sketches, show our method achieves state-of-the-art performance with respect to both average inference accuracy and total memory cost.

Improving COVID-19 CT Classification of CNNs by Learning Parameter-Efficient Representation

COVID-19 pandemic continues to spread rapidly over the world and causes a tremendous crisis in global human health and the economy. Its early detection and diagnosis are crucial for controlling the further spread. Many deep learning-based methods have been proposed to assist clinicians in automatic COVID-19 diagnosis based on computed tomography imaging. However, challenges still remain, including low data diversity in existing datasets, and unsatisfied detection resulting from insufficient accuracy and sensitivity of deep learning models. To enhance the data diversity, we design augmentation techniques of incremental levels and apply them to the largest open-access benchmark dataset, COVIDx CT-2A. Meanwhile, similarity regularization (SR) derived from contrastive learning is proposed in this study to enable CNNs to learn more parameter-efficient representations, thus improving the accuracy and sensitivity of CNNs. The results on seven commonly used CNNs demonstrate that CNN performance can be improved stably through applying the designed augmentation and SR techniques. In particular, DenseNet121 with SR achieves an average test accuracy of 99.44% in three trials for three-category classification, including normal, non-COVID-19 pneumonia, and COVID-19 pneumonia. And the achieved precision, sensitivity, and specificity for the COVID-19 pneumonia category are 98.40%, 99.59%, and 99.50%, respectively. These statistics suggest that our method has surpassed the existing state-of-the-art methods on the COVIDx CT-2A dataset.

MIIDL: a Python package for microbial biomarkers identification powered by interpretable deep learning

Detecting microbial biomarkers used to predict disease phenotypes and clinical outcomes is crucial for disease early-stage screening and diagnosis. Most methods for biomarker identification are linear-based, which is very limited as biological processes are rarely fully linear. The introduction of machine learning to this field tends to bring a promising solution. However, identifying microbial biomarkers in an interpretable, data-driven and robust manner remains challenging. We present MIIDL, a Python package for the identification of microbial biomarkers based on interpretable deep learning. MIIDL innovatively applies convolutional neural networks, a variety of interpretability algorithms and plenty of pre-processing methods to provide a one-stop and robust pipeline for microbial biomarkers identification from high-dimensional and sparse data sets.

IB-DRR: Incremental Learning with Information-Back Discrete Representation Replay

Incremental learning aims to enable machine learning models to continuously acquire new knowledge given new classes, while maintaining the knowledge already learned for old classes. Saving a subset of training samples of previously seen classes in the memory and replaying them during new training phases is proven to be an efficient and effective way to fulfil this aim. It is evident that the larger number of exemplars the model inherits the better performance it can achieve. However, finding a trade-off between the model performance and the number of samples to save for each class is still an open problem for replay-based incremental learning and is increasingly desirable for real-life applications. In this paper, we approach this open problem by tapping into a two-step compression approach. The first step is a lossy compression, we propose to encode input images and save their discrete latent representations in the form of codes that are learned using a hierarchical Vector Quantised Variational Autoencoder (VQ-VAE). In the second step, we further compress codes losslessly by learning a hierarchical latent variable model with bits-back asymmetric numeral systems (BB-ANS). To compensate for the information lost in the first step compression, we introduce an Information Back (IB) mechanism that utilizes real exemplars for a contrastive learning loss to regularize the training of a classifier. By maintaining all seen exemplars' representations in the format of `codes', Discrete Representation Replay (DRR) outperforms the state-of-art method on CIFAR-100 by a margin of 4% accuracy with a much less memory cost required for saving samples. Incorporated with IB and saving a small set of old raw exemplars as well, the accuracy of DRR can be further improved by 2% accuracy.

DeepFaceLab: A simple, flexible and extensible face swapping framework

DeepFaceLab is an open-source deepfake system created by \textbf{iperov} for face swapping with more than 3,000 forks and 13,000 stars in Github: it provides an imperative and easy-to-use pipeline for people to use with no comprehensive understanding of deep learning framework or with model implementation required, while remains a flexible and loose coupling structure for people who need to strengthen their own pipeline with other features without writing complicated boilerplate code. In this paper, we detail the principles that drive the implementation of DeepFaceLab and introduce the pipeline of it, through which every aspect of the pipeline can be modified painlessly by users to achieve their customization purpose, and it's noteworthy that DeepFaceLab could achieve results with high fidelity and indeed indiscernible by mainstream forgery detection approaches. We demonstrate the advantage of our system through comparing our approach with current prevailing systems. For more information, please visit: https://github.com/iperov/DeepFaceLab/.