Search

Studies of the mouse visual system have revealed a variety of visual brain areas that are thought to support a multitude of behavioral capacities, ranging from stimulus-reward associations, to goal-directed navigation, and object-centric discriminations. However, an overall understanding of the mouse's visual cortex, and how it supports a range of behaviors, remains unknown. Here, we take a computational approach to help address these questions, providing a high-fidelity quantitative model of mouse visual cortex and identifying key structural and functional principles underlying that model's success. Structurally, we find that a comparatively shallow network structure with a low-resolution input is optimal for modeling mouse visual cortex. Our main finding is functional—that models trained with task-agnostic, self-supervised objective functions based on the concept of contrastive embeddings are much better matches to mouse cortex, than models trained on supervised objectives or alternative self-supervised methods. This result is very much unlike in primates where prior work showed that the two were roughly equivalent, naturally leading us to ask the question of why these self-supervised objectives are better matches than supervised ones in mouse. To this end, we show that the self-supervised, contrastive objective builds a general-purpose visual representation that enables the system to achieve better transfer on out-of-distribution visual scene understanding and reward-based navigation tasks. Our results suggest that mouse visual cortex is a low-resolution, shallow network that makes best use of the mouse's limited resources to create a light-weight, general-purpose visual system—in contrast to the deep, high-resolution, and more categorization-dominated visual system of primates. Author summary: Studies of mouse visual behavior have revealed a multitude of visual abilities, ranging from stimulus-reward associations, to goal-directed navigation, and object-centric discriminations. A principled system-wide model of mouse visual cortex would be useful both in providing an organizing theory for this wide spectrum of behaviors, and enabling practical technology for many model-driven studies of mouse neuroscience more broadly. However, the standard approach to creating quantitatively accurate models of primate visual cortex has been less successful with the mouse system. Here we identify critical computational features needed to capture mouse-specific neural stimulus-response patterns, and illustrate how these features can be interpreted as giving the highly resource-limited mouse brain a comparative advantage in self-learning a task-general visual representation. [ABSTRACT FROM AUTHOR]

In reversal learning tasks, the behavior of humans and animals is often assumed to be uniform within single experimental sessions to facilitate data analysis and model fitting. However, behavior of agents can display substantial variability in single experimental sessions, as they execute different blocks of trials with different transition dynamics. Here, we observed that in a deterministic reversal learning task, mice display noisy and sub-optimal choice transitions even at the expert stages of learning. We investigated two sources of the sub-optimality in the behavior. First, we found that mice exhibit a high lapse rate during task execution, as they reverted to unrewarded directions after choice transitions. Second, we unexpectedly found that a majority of mice did not execute a uniform strategy, but rather mixed between several behavioral modes with different transition dynamics. We quantified the use of such mixtures with a state-space model, block Hidden Markov Model (block HMM), to dissociate the mixtures of dynamic choice transitions in individual blocks of trials. Additionally, we found that blockHMM transition modes in rodent behavior can be accounted for by two different types of behavioral algorithms, model-free or inference-based learning, that might be used to solve the task. Combining these approaches, we found that mice used a mixture of both exploratory, model-free strategies and deterministic, inference-based behavior in the task, explaining their overall noisy choice sequences. Together, our combined computational approach highlights intrinsic sources of noise in rodent reversal learning behavior and provides a richer description of behavior than conventional techniques, while uncovering the hidden states that underlie the block-by-block transitions. Author summary: Humans and animals can use diverse decision-making strategies to maximize rewards in uncertain environments, but previous studies have not investigated the use of multiple strategies that involve distinct latent switching dynamics in reward-guided behavior. Here, using a reversal learning task, we showed that mice displayed a much more variable behavior than would be expected from a uniform strategy, suggesting that they mix between multiple behavioral modes in the task. We develop a computational method to dissociate these learning modes from behavioral data, addressing the challenges faced by current analytical methods when agents mix between different strategies. We found that the use of multiple strategies is a key feature of rodent behavior even in the expert stages of learning, and applied our tools to quantify the highly diverse strategies used by individual mice in the task. We further mapped these behavioral modes to two types of underlying algorithms, model-free Q-learning and inference-based behavior. These rich descriptions of underlying latent states form the basis of detecting abnormal patterns of behavior in reward-guided decision-making. [ABSTRACT FROM AUTHOR]

The mouse brain contains a rich diversity of inhibitory neuron types that have been characterized by their patterns of gene expression. However, it is still unclear how these cell types are distributed across the mouse brain. We developed a computational method to estimate the densities of different inhibitory neuron types across the mouse brain. Our method allows the unbiased integration of diverse and disparate datasets into one framework to predict inhibitory neuron densities for uncharted brain regions. We constrained our estimates based on previously computed brain-wide neuron densities, gene expression data from in situ hybridization image stacks together with a wide range of values reported in the literature. Using constrained optimization, we derived coherent estimates of cell densities for the different inhibitory neuron types. We estimate that 20.3% of all neurons in the mouse brain are inhibitory. Among all inhibitory neurons, 18% predominantly express parvalbumin (PV), 16% express somatostatin (SST), 3% express vasoactive intestinal peptide (VIP), and the remainder 63% belong to the residual GABAergic population. We find that our density estimations improve as more literature values are integrated. Our pipeline is extensible, allowing new cell types or data to be integrated as they become available. The data, algorithms, software, and results of our pipeline are publicly available and update the Blue Brain Cell Atlas. This work therefore leverages the research community to collectively converge on the numbers of each cell type in each brain region. Author summary: Obtaining a global understanding of the cellular composition of the brain is a very complex task, not only because of the great variability that exists between reports of similar counts but also because of the numerous brain regions and cell types that make up the brain. Previously, we presented a model of a cell atlas, which provided an estimate of the densities of neurons, glia and their subtypes for each region in the mouse brain. Here, we describe an extension of this model to include more inhibitory neuron types. We collected estimates of inhibitory neuron counts from literature and built a framework to combine them into a consistent cell atlas. Using brain slice images, we also estimated inhibitory neuron density in regions where no literature data are available. We estimated that in the mouse brain 20.3% of all neurons are inhibitory. Among all inhibitory neurons, 18% predominantly express parvalbumin (PV), 16% express somatostatin (SST), 3% express vasoactive intestinal peptide (VIP), and the remainder 63% belong to the residual GABAergic population. Our approach can be further extended to any other cell type and provides a resource to build tissue-level models of the rodent brain. [ABSTRACT FROM AUTHOR]

Short-read RNA sequencing and long-read RNA sequencing each have their strengths and weaknesses for transcriptome assembly. While short reads are highly accurate, they are rarely able to span multiple exons. Long-read technology can capture full-length transcripts, but its relatively high error rate often leads to mis-identified splice sites. Here we present a new release of StringTie that performs hybrid-read assembly. By taking advantage of the strengths of both long and short reads, hybrid-read assembly with StringTie is more accurate than long-read only or short-read only assembly, and on some datasets it can more than double the number of correctly assembled transcripts, while obtaining substantially higher precision than the long-read data assembly alone. Here we demonstrate the improved accuracy on simulated data and real data from Arabidopsis thaliana, Mus musculus, and human. We also show that hybrid-read assembly is more accurate than correcting long reads prior to assembly while also being substantially faster. StringTie is freely available as open source software at https://github.com/gpertea/stringtie. Author summary: Identifying the genes that are active in a cell is a critical step in studying cell development, disease, the response to infection, the effects of mutations, and much more. During the last decade, high-throughput RNA-sequencing data have proven essential in characterizing the set of genes expressed in different cell types and conditions, which has driven a strong need for highly efficient, scalable and accurate computational methods to process these data. As sequencing costs have dropped, ever-larger experiments have been designed, often capturing hundreds of millions or even billions of reads in a single study. These enormous data sets require highly efficient and accurate computational methods for analysis, and they also present opportunities for discovery. Recently developed long-read technology now allows researchers to capture entire transcripts in a single long read, enabling more accurate reconstruction of the full exon-intron structure of genes, although these reads have higher error rates and higher costs. In this study we use the high accuracy of short reads to correct the alignments of long RNA reads, with the goal of improving the identification of novel gene isoforms, and ultimately our understanding of transcriptome complexity. [ABSTRACT FROM AUTHOR]

House mice communicate through ultrasonic vocalizations (USVs), which are above the range of human hearing (>20 kHz), and several automated methods have been developed for USV detection and classification. Here we evaluate their advantages and disadvantages in a full, systematic comparison, while also presenting a new approach. This study aims to 1) determine the most efficient USV detection tool among the existing methods, and 2) develop a classification model that is more generalizable than existing methods. In both cases, we aim to minimize the user intervention required for processing new data. We compared the performance of four detection methods in an out-of-the-box approach, pretrained DeepSqueak detector, MUPET, USVSEG, and the Automatic Mouse Ultrasound Detector (A-MUD). We also compared these methods to human visual or 'manual' classification (ground truth) after assessing its reliability. A-MUD and USVSEG outperformed the other methods in terms of true positive rates using default and adjusted settings, respectively, and A-MUD outperformed USVSEG when false detection rates were also considered. For automating the classification of USVs, we developed BootSnap for supervised classification, which combines bootstrapping on Gammatone Spectrograms and Convolutional Neural Networks algorithms with Snapshot ensemble learning. It successfully classified calls into 12 types, including a new class of false positives that is useful for detection refinement. BootSnap outperformed the pretrained and retrained state-of-the-art tool, and thus it is more generalizable. BootSnap is freely available for scientific use. Author summary: House mice and many other species use ultrasonic vocalizations to communicate in various contexts including social and sexual interactions. These vocalizations are increasingly investigated in research on animal communication and as a phenotype for studying the genetic basis of autism and speech disorders. Because manual methods for analyzing vocalizations are extremely time consuming, automatic tools for detection and classification are needed. We evaluated the performance of the available tools for analyzing ultrasonic vocalizations, and we compared detection tools for the first time to manual methods ("ground truth") using recordings from wild-derived and laboratory mice. For the first time, class-wise inter-observer reliability of manual labels used for ground truth are analyzed and reported. Moreover, we developed a new classification method based on ensemble deep learning that provides more generalizability than the current state-of-the-art tool (both pretrained and retrained). Our new classification method is free for scientific use. [ABSTRACT FROM AUTHOR]