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Abstract Predictions of biodiversity trajectories under climate change are crucial in order to act effectively in maintaining the diversity of species. In many ecological applications, future predictions are made under various global warming scenarios, as described by a range of different climate models. We propose a clustering methodology to synthesize and interpret the outputs of these various predictions.We propose an interpretable and flexible two‐step methodology to measure the similarity between predicted species range maps and to cluster the future scenario predictions utilizing a spectral clustering technique. We implement and provide code for this method.We find that clustering based on predicted species range maps is mainly driven by the amount of warming rather than climate model or future scenario. We contrast this with clustering based only on predicted climate variables, which is driven primarily by climate models, that is, scenarios of the same climate model are clustered together, even when the amount of warming input to the models is varied.The differences between species‐based and climate‐based clusterings illustrate that it is crucial to incorporate ecological information to understand the relevant differences between climate models. Our findings can be used to better synthesize forecasts of biodiversity change under the wide spectrum of results that emerge when considering potential future scenarios. 

Abstract Anomaly detection aims to identify observations that deviate from the typical pattern of data. Anomalous observations may correspond to financial fraud, health risks, or incorrectly measured data in practice. We focus on unsupervised detection and the continuous and categorical (mixed) variable case. We show that detecting anomalies in mixed data is enhanced through first embedding the data then assessing an anomaly scoring scheme. We propose a kurtosis‐weightedFactor Analysis of Mixed Datafor anomaly detection to obtain a continuous embedding for anomaly scoring. We illustrate that anomalies are highly separable in the first and last few ordered dimensions of this space, and test various anomaly scoring experiments within this subspace. Results are illustrated for both simulated and real datasets, and the proposed approach is highly accurate for mixed data throughout these diverse scenarios. 

Abstract Spatially resolved in situ transmission electron microscopy (TEM), equipped with direct electron detection systems, is a suitable technique to record information about the atom-scale dynamics with millisecond temporal resolution from materials. However, characterizing dynamics or fluxional behavior requires processing short time exposure images which usually have severely degraded signal-to-noise ratios. The poor signal-to-noise associated with high temporal resolution makes it challenging to determine the position and intensity of atomic columns in materials undergoing structural dynamics. To address this challenge, we propose a noise-robust, processing approach based on blob detection, which has been previously established for identifying objects in images in the community of computer vision. In particular, a blob detection algorithm has been tailored to deal with noisy TEM image series from nanoparticle systems. In the presence of high noise content, our blob detection approach is demonstrated to outperform the results of other algorithms, enabling the determination of atomic column position and its intensity with a higher degree of precision. 

Abstract A deep convolutional neural network has been developed to denoise atomic-resolution transmission electron microscope image datasets of nanoparticles acquired using direct electron counting detectors, for applications where the image signal is severely limited by shot noise. The network was applied to a model system of CeO2-supported Pt nanoparticles. We leverage multislice image simulations to generate a large and flexible dataset for training the network. The proposed network outperforms state-of-the-art denoising methods on both simulated and experimental test data. Factors contributing to the performance are identified, including (a) the geometry of the images used during training and (b) the size of the network's receptive field. Through a gradient-based analysis, we investigate the mechanisms learned by the network to denoise experimental images. This shows that the network exploits both extended and local information in the noisy measurements, for example, by adapting its filtering approach when it encounters atomic-level defects at the nanoparticle surface. Extensive analysis has been done to characterize the network's ability to correctly predict the exact atomic structure at the nanoparticle surface. Finally, we develop an approach based on the log-likelihood ratio test that provides a quantitative measure of the agreement between the noisy observation and the atomic-level structure in the network-denoised image. 

Abstract We present new methods for cell line classification using multivariate time series bioimpedance data obtained from electric cell-substrate impedance sensing (ECIS) technology. The ECIS technology, which monitors the attachment and spreading of mammalian cells in real time through the collection of electrical impedance data, has historically been used to study one cell line at a time. However, we show that if applied to data from multiple cell lines, ECIS can be used to classify unknown or potentially mislabeled cells, factors which have previously been associated with the reproducibility crisis in the biological literature. We assess a range of approaches to this new problem, testing different classification methods and deriving a dictionary of 29 features to characterize ECIS data. Most notably, our analysis enriches the current field by making use of simultaneous multi-frequency ECIS data, where previous studies have focused on only one frequency; using classification methods to distinguish multiple cell lines, rather than simple statistical tests that compare only two cell lines; and assessing a range of features derived from ECIS data based on their classification performance. In classification tests on fifteen mammalian cell lines, we obtain very high out-of-sample predictive accuracy. These preliminary findings provide a baseline for future large-scale studies in this field.