Understanding the relationship between behavior and neural activity is crucial for understanding brain function. An effective method is to learn embeddings for interconnected modalities. For simple behavioral tasks, neural features can be learned based on labels. However, complex behaviors, such as social interactions, require the joint extraction of behavioral and neural characteristics. In this paper, we present an autoencoder (AE) framework, called Shared-AE, which includes a novel regularization term that automatically identifies features shared between neural activity and behavior, while simultaneously capturing the unique private features specific to each modality. We apply Shared-AE to large-scale neural activity recorded across the entire dorsal cortex of the mouse, during two very different behaviors: (i) head-fixed mice performing a self-initiated decision-making task, and (ii) freely-moving social behavior amongst two mice. Our model successfully captures both `shared features', shared across neural and behavioral activity, and `private features', unique to each modality, significantly enhancing our understanding of the alignment between neural activity and complex behaviors. The original code for the entire Shared-AE framework on Pytorch has been made publicly available at: \url{https://github.com/saxenalab-neuro/Shared-AE}.

Large volumes of used electronics are often collected in remanufacturing plants, which requires disassembly before harvesting parts for reuse. Disassembly is mainly conducted manually with low productivity. Recently, human–robot collaboration has been considered as a solution. To assist effectively, robots should observe work environments and recognize human actions accurately. Rich activity video recording and supervised learning can be used to extract insights; however, supervised learning does not allow robots to self-accomplish the learning process. This study proposes an unsupervised learning framework for achieving video-based human activity recognition. The framework consists of two main elements: 1) a variational-autoencoder-based architecture for unlabeled data representation learning and 2) a hidden Markov model for activity state division. The complete explicit activity classification is validated against ground truth labels; here, we use a case study of disassembling a hard disk drive. The framework shows an average recognition accuracy of 91.52%, higher than competing methods.

The rapid development of machine learning and deep learning algorithms in the recent decade has spurred an outburst of their applications in many research fields. In the chemistry domain, machine learning has been widely used to aid in drug screening, drug toxicity prediction, quantitative structure-activity relationship prediction, anti-cancer synergy score prediction, etc. This review is dedicated to the application of machine learning in drug response prediction. Specifically, we focus on molecular representations, which is a crucial element to the success of drug response prediction and other chemistry-related prediction tasks. We introduce three types of commonly used molecular representation methods, together with their implementation and application examples. This review will serve as a brief introduction of the broad field of molecular representations.

Studying isoform expression at the microscopic level has always been a challenging task. A classical example is kidney, where glomerular and tubulo-interstitial compartments carry out drastically different physiological functions and thus presumably their isoform expression also differs. We aim at developing an experimental and computational pipeline for identifying isoforms at microscopic structure-level. We microdissected glomerular and tubulo-interstitial compartments from healthy human kidney tissues from two cohorts. The two compartments were separately sequenced with the PacBio RS II platform. These transcripts were then validated using transcripts of the same samples by the traditional Illumina RNA-Seq protocol, distinct Illumina RNA-Seq short reads from European Renal cDNA Bank (ERCB) samples, and annotated GENCODE transcript list, thus identifying novel transcripts. We identified 14,739 and 14,259 annotated transcripts, and 17,268 and 13,118 potentially novel transcripts in the glomerular and tubulo-interstitial compartments, respectively. Of note, relying solely on either short or long reads would have resulted in many erroneous identifications. We identified distinct pathways involved in glomerular and tubulo-interstitial compartments at the isoform level, creating an important experimental and computational resource for the kidney research community.