HTC-retina: A hybrid retinal diseases classification model using transformer-Convolutional Neural Network from optical coherence tomography images.

Retinal diseases are among nowadays major public health issues, deservedly needing advanced computer-aided diagnosis. We propose a hybrid model for multi label classification, whereby seven retinal diseases are automatically classified from Optical Coherence Tomography (OCT) images. We show that, by combining the strengths of Convolutional Neural Networks (CNNs) and Visual Transformers (ViTs), we can produce a more powerful type of model for medical image classification, especially when considering local lesion information such as retinal diseases. CNNs are indeed proved to be efficient at parameter utilization and provide the ability to extract local features and multi-scale feature maps through convolutional operations. On the other hand, ViT's self-attention procedure allows processing long-range and global dependencies within an image. The paper clearly shows that the hybridization of these complementary capabilities (CNNs-ViTs) presents a high image processing potential that is more robust and efficient. The proposed model adopts a hierarchical CNN module called Convolutional Patch and Token Embedding (CPTE) instead of employing a direct tokenization approach using the raw input OCT image in the transformer. The CPTE module's role is to incorporate an inductive bias, to reduce the reliance on large-scale datasets, and to address the low-level feature extraction challenges of the ViT. In addition, considering the importance of local lesion information in OCT images, the model relies on a parallel module called Residual Depthwise-Pointwise ConvNet (RDP-ConvNet) for extracting high-level features. RDP-ConvNet utilizes depthwise and pointwise convolution layers within a residual network architecture. The overall performance of the HTC-Retina model was evaluated on three datasets: the OCT-2017, OCT-C8, and OCT-2014 ; outperforming previous established models, achieving accuracy rates of 99.40%, 97.00%, and 99.77%, respectively ; and sensitivity rates of 99.41%, 97.00%, and 99.77%, respectively. Notably, the model showed high performance while maintaining computational efficiency.

State of the art of fuzzy methods for gene regulatory networks inference.

To address one of the most challenging issues at the cellular level, this paper surveys the fuzzy methods used in gene regulatory networks (GRNs) inference. GRNs represent causal relationships between genes that have a direct influence, trough protein production, on the life and the development of living organisms and provide a useful contribution to the understanding of the cellular functions as well as the mechanisms of diseases. Fuzzy systems are based on handling imprecise knowledge, such as biological information. They provide viable computational tools for inferring GRNs from gene expression data, thus contributing to the discovery of gene interactions responsible for specific diseases and/or ad hoc correcting therapies. Increasing computational power and high throughput technologies have provided powerful means to manage these challenging digital ecosystems at different levels from cell to society globally. The main aim of this paper is to report, present, and discuss the main contributions of this multidisciplinary field in a coherent and structured framework.