ABSTRACT
The molecular clock model is fundamental for inferring species divergence times from molecular sequences. However, its direct application may introduce significant biases due to sequencing errors, recombination events, and inaccurately labeled sampling times. Improving accuracy necessitates rigorous quality control measures to identify and remove potentially erroneous sequences. Furthermore, while not all branches of a phylogenetic tree may exhibit a clear temporal signal, specific branches may still adhere to the assumptions, with varying evolutionary rates. Supporting a relaxed molecular clock model better aligns with the complexities of evolution. The root-to-tip regression method has been widely used to analyze the temporal signal in phylogenetic studies and can be generalized for detecting other phylogenetic signals. Despite its utility, there remains a lack of corresponding software implementations for broader applications. To address this gap, we present shinyTempSignal, an interactive web application implemented with the shiny framework, available as an R package and publicly accessible at https://github.com/YuLab-SMU/shinyTempSignal. This tool facilitates the analysis of temporal and other phylogenetic signals under both strict and relaxed models. By extending the root-to-tip regression method to diverse signals, shinyTempSignal helps in the detection of evolving features or traits, thereby laying the foundation for deeper insights and subsequent analyses.
ABSTRACT
The visual system provides a valuable model for studying the working mechanisms of sensory processing and high-level consciousness. A significant challenge in this field is the reconstruction of images from decoded neural activity, which could not only test the accuracy of our understanding of the visual system but also provide a practical tool for solving real-world problems. Although recent advances in deep learning have improved the decoding of neural spike trains, little attention has been paid to the underlying mechanisms of the visual system. To address this issue, we propose a deep learning neural network architecture that incorporates the biological properties of the visual system, such as receptive fields, to reconstruct visual images from spike trains. Our model outperforms current models and has been evaluated on different datasets from both retinal ganglion cells (RGCs) and the primary visual cortex (V1) neural spikes. Our model demonstrated the great potential of brain-inspired algorithms to solve a challenge that our brain solves.
