Brandon Carter

Lucas Liebenwein, Cenk Baykal, Brandon Carter et al.

Neural network pruning is a popular technique used to reduce the inference costs of modern, potentially overparameterized, networks. Starting from a pre-trained network, the process is as follows: remove redundant parameters, retrain, and repeat while maintaining the same test accuracy. The result is a model that is a fraction of the size of the original with comparable predictive performance (test accuracy). Here, we reassess and evaluate whether the use of test accuracy alone in the terminating condition is sufficient to ensure that the resulting model performs well across a wide spectrum of "harder" metrics such as generalization to out-of-distribution data and resilience to noise. Across evaluations on varying architectures and data sets, we find that pruned networks effectively approximate the unpruned model, however, the prune ratio at which pruned networks achieve commensurate performance varies significantly across tasks. These results call into question the extent of \emph{genuine} overparameterization in deep learning and raise concerns about the practicability of deploying pruned networks, specifically in the context of safety-critical systems, unless they are widely evaluated beyond test accuracy to reliably predict their performance. Our code is available at https://github.com/lucaslie/torchprune.

Ge Liu, Alexander Dimitrakakis, Brandon Carter et al.

We introduce the maximum $n$-times coverage problem that selects $k$ overlays to maximize the summed coverage of weighted elements, where each element must be covered at least $n$ times. We also define the min-cost $n$-times coverage problem where the objective is to select the minimum set of overlays such that the sum of the weights of elements that are covered at least $n$ times is at least $τ$. Maximum $n$-times coverage is a generalization of the multi-set multi-cover problem, is NP-complete, and is not submodular. We introduce two new practical solutions for $n$-times coverage based on integer linear programming and sequential greedy optimization. We show that maximum $n$-times coverage is a natural way to frame peptide vaccine design, and find that it produces a pan-strain COVID-19 vaccine design that is superior to 29 other published designs in predicted population coverage and the expected number of peptides displayed by each individual's HLA molecules.

Brandon Carter, Siddhartha Jain, Jonas Mueller et al.

Image classifiers are typically scored on their test set accuracy, but high accuracy can mask a subtle type of model failure. We find that high scoring convolutional neural networks (CNNs) on popular benchmarks exhibit troubling pathologies that allow them to display high accuracy even in the absence of semantically salient features. When a model provides a high-confidence decision without salient supporting input features, we say the classifier has overinterpreted its input, finding too much class-evidence in patterns that appear nonsensical to humans. Here, we demonstrate that neural networks trained on CIFAR-10 and ImageNet suffer from overinterpretation, and we find models on CIFAR-10 make confident predictions even when 95% of input images are masked and humans cannot discern salient features in the remaining pixel-subsets. We introduce Batched Gradient SIS, a new method for discovering sufficient input subsets for complex datasets, and use this method to show the sufficiency of border pixels in ImageNet for training and testing. Although these patterns portend potential model fragility in real-world deployment, they are in fact valid statistical patterns of the benchmark that alone suffice to attain high test accuracy. Unlike adversarial examples, overinterpretation relies upon unmodified image pixels. We find ensembling and input dropout can each help mitigate overinterpretation.

Angie Boggust, Brandon Carter, Arvind Satyanarayan

Embeddings mapping high-dimensional discrete input to lower-dimensional continuous vector spaces have been widely adopted in machine learning applications as a way to capture domain semantics. Interviewing 13 embedding users across disciplines, we find comparing embeddings is a key task for deployment or downstream analysis but unfolds in a tedious fashion that poorly supports systematic exploration. In response, we present the Embedding Comparator, an interactive system that presents a global comparison of embedding spaces alongside fine-grained inspection of local neighborhoods. It systematically surfaces points of comparison by computing the similarity of the $k$-nearest neighbors of every embedded object between a pair of spaces. Through case studies across multiple modalities, we demonstrate our system rapidly reveals insights, such as semantic changes following fine-tuning, language changes over time, and differences between seemingly similar models. In evaluations with 15 participants, we find our system accelerates comparisons by shifting from laborious manual specification to browsing and manipulating visualizations.

Brandon Carter, Jonas Mueller, Siddhartha Jain et al.

Local explanation frameworks aim to rationalize particular decisions made by a black-box prediction model. Existing techniques are often restricted to a specific type of predictor or based on input saliency, which may be undesirably sensitive to factors unrelated to the model's decision making process. We instead propose sufficient input subsets that identify minimal subsets of features whose observed values alone suffice for the same decision to be reached, even if all other input feature values are missing. General principles that globally govern a model's decision-making can also be revealed by searching for clusters of such input patterns across many data points. Our approach is conceptually straightforward, entirely model-agnostic, simply implemented using instance-wise backward selection, and able to produce more concise rationales than existing techniques. We demonstrate the utility of our interpretation method on various neural network models trained on text, image, and genomic data.