Improving Out-of-Distribution Robustness via Selective Augmentation

Machine learning algorithms typically assume that training and test examples are drawn from the same distribution. However, distribution shift is a common problem in real-world applications and can cause models to perform dramatically worse at test time. In this paper, we specifically consider the problems of domain shifts and subpopulation shifts (eg. imbalanced data). While prior works often seek to explicitly regularize internal representations and predictors of the model to be domain invariant, we instead aim to regularize the whole function without restricting the model's internal representations. This leads to a simple mixup-based technique which learns invariant functions via selective augmentation called LISA. LISA selectively interpolates samples either with the same labels but different domains or with the same domain but different labels. We analyze a linear setting and theoretically show how LISA leads to a smaller worst-group error. Empirically, we study the effectiveness of LISA on nine benchmarks ranging from subpopulation shifts to domain shifts, and we find that LISA consistently outperforms other state-of-the-art methods.

How to Learn when Data Gradually Reacts to Your Model

A recent line of work has focused on training machine learning (ML) models in the performative setting, i.e. when the data distribution reacts to the deployed model. The goal in this setting is to learn a model which both induces a favorable data distribution and performs well on the induced distribution, thereby minimizing the test loss. Previous work on finding an optimal model assumes that the data distribution immediately adapts to the deployed model. In practice, however, this may not be the case, as the population may take time to adapt to the model. In many applications, the data distribution depends on both the currently deployed ML model and on the "state" that the population was in before the model was deployed. In this work, we propose a new algorithm, Stateful Performative Gradient Descent (Stateful PerfGD), for minimizing the performative loss even in the presence of these effects. We provide theoretical guarantees for the convergence of Stateful PerfGD. Our experiments confirm that Stateful PerfGD substantially outperforms previous state-of-the-art methods.

Beyond Importance Scores: Interpreting Tabular ML by Visualizing Feature Semantics

Interpretability is becoming an active research topic as machine learning (ML) models are more widely used to make critical decisions. Tabular data is one of the most commonly used modes of data in diverse applications such as healthcare and finance. Much of the existing interpretability methods used for tabular data only report feature-importance scores -- either locally (per example) or globally (per model) -- but they do not provide interpretation or visualization of how the features interact. We address this limitation by introducing Feature Vectors, a new global interpretability method designed for tabular datasets. In addition to providing feature-importance, Feature Vectors discovers the inherent semantic relationship among features via an intuitive feature visualization technique. Our systematic experiments demonstrate the empirical utility of this new method by applying it to several real-world datasets. We further provide an easy-to-use Python package for Feature Vectors.

Disparities in Dermatology AI: Assessments Using Diverse Clinical Images

More than 3 billion people lack access to care for skin disease. AI diagnostic tools may aid in early skin cancer detection; however most models have not been assessed on images of diverse skin tones or uncommon diseases. To address this, we curated the Diverse Dermatology Images (DDI) dataset - the first publicly available, pathologically confirmed images featuring diverse skin tones. We show that state-of-the-art dermatology AI models perform substantially worse on DDI, with ROC-AUC dropping 29-40 percent compared to the models' original results. We find that dark skin tones and uncommon diseases, which are well represented in the DDI dataset, lead to performance drop-offs. Additionally, we show that state-of-the-art robust training methods cannot correct for these biases without diverse training data. Our findings identify important weaknesses and biases in dermatology AI that need to be addressed to ensure reliable application to diverse patients and across all disease.

Explaining medical AI performance disparities across sites with confounder Shapley value analysis

Medical AI algorithms can often experience degraded performance when evaluated on previously unseen sites. Addressing cross-site performance disparities is key to ensuring that AI is equitable and effective when deployed on diverse patient populations. Multi-site evaluations are key to diagnosing such disparities as they can test algorithms across a broader range of potential biases such as patient demographics, equipment types, and technical parameters. However, such tests do not explain why the model performs worse. Our framework provides a method for quantifying the marginal and cumulative effect of each type of bias on the overall performance difference when a model is evaluated on external data. We demonstrate its usefulness in a case study of a deep learning model trained to detect the presence of pneumothorax, where our framework can help explain up to 60% of the discrepancy in performance across different sites with known biases like disease comorbidities and imaging parameters.

Beta Shapley: a Unified and Noise-reduced Data Valuation Framework for Machine Learning

Data Shapley has recently been proposed as a principled framework to quantify the contribution of individual datum in machine learning. It can effectively identify helpful or harmful data points for a learning algorithm. In this paper, we propose Beta Shapley, which is a substantial generalization of Data Shapley. Beta Shapley arises naturally by relaxing the efficiency axiom of the Shapley value, which is not critical for machine learning settings. Beta Shapley unifies several popular data valuation methods and includes data Shapley as a special case. Moreover, we prove that Beta Shapley has several desirable statistical properties and propose efficient algorithms to estimate it. We demonstrate that Beta Shapley outperforms state-of-the-art data valuation methods on several downstream ML tasks such as: 1) detecting mislabeled training data; 2) learning with subsamples; and 3) identifying points whose addition or removal have the largest positive or negative impact on the model.

CloudPred: Predicting Patient Phenotypes From Single-cell RNA-seq

Single-cell RNA sequencing (scRNA-seq) has the potential to provide powerful, high-resolution signatures to inform disease prognosis and precision medicine. This paper takes an important first step towards this goal by developing an interpretable machine learning algorithm, CloudPred, to predict individuals' disease phenotypes from their scRNA-seq data. Predicting phenotype from scRNA-seq is challenging for standard machine learning methods -- the number of cells measured can vary by orders of magnitude across individuals and the cell populations are also highly heterogeneous. Typical analysis creates pseudo-bulk samples which are biased toward prior annotations and also lose the single cell resolution. CloudPred addresses these challenges via a novel end-to-end differentiable learning algorithm which is coupled with a biologically informed mixture of cell types model. CloudPred automatically infers the cell subpopulation that are salient for the phenotype without prior annotations. We developed a systematic simulation platform to evaluate the performance of CloudPred and several alternative methods we propose, and find that CloudPred outperforms the alternative methods across several settings. We further validated CloudPred on a real scRNA-seq dataset of 142 lupus patients and controls. CloudPred achieves AUROC of 0.98 while identifying a specific subpopulation of CD4 T cells whose presence is highly indicative of lupus. CloudPred is a powerful new framework to predict clinical phenotypes from scRNA-seq data and to identify relevant cells.

Clustering Plotted Data by Image Segmentation

Clustering algorithms are one of the main analytical methods to detect patterns in unlabeled data. Existing clustering methods typically treat samples in a dataset as points in a metric space and compute distances to group together similar points. In this paper, we present a wholly different way of clustering points in 2-dimensional space, inspired by how humans cluster data: by training neural networks to perform instance segmentation on plotted data. Our approach, Visual Clustering, has several advantages over traditional clustering algorithms: it is much faster than most existing clustering algorithms (making it suitable for very large datasets), it agrees strongly with human intuition for clusters, and it is by default hyperparameter free (although additional steps with hyperparameters can be introduced for more control of the algorithm). We describe the method and compare it to ten other clustering methods on synthetic data to illustrate its advantages and disadvantages. We then demonstrate how our approach can be extended to higher dimensional data and illustrate its performance on real-world data. The implementation of Visual Clustering is publicly available and can be applied to any dataset in a few lines of code.

The Power of Contrast for Feature Learning: A Theoretical Analysis

Contrastive learning has achieved state-of-the-art performance in various self-supervised learning tasks and even outperforms its supervised counterpart. Despite its empirical success, theoretical understanding of why contrastive learning works is still limited. In this paper, (i) we provably show that contrastive learning outperforms autoencoder, a classical unsupervised learning method, for both feature recovery and downstream tasks; (ii) we also illustrate the role of labeled data in supervised contrastive learning. This provides theoretical support for recent findings that contrastive learning with labels improves the performance of learned representations in the in-domain downstream task, but it can harm the performance in transfer learning. We verify our theory with numerical experiments.