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Yiqun T. Chen

Publications and source records attributed to Yiqun T. Chen.

7 recordsLinked to original sources

Power Analysis for Prediction-Powered Inference

Modern studies increasingly leverage outcomes predicted by machine learning and artificial intelligence (AI/ML) models, and recent work, such as prediction-powered inference (PPI), has developed valid downstream statistical inference procedures. However, classical power and sample size formulas do not readily account for these predictions. In this work, we tackle a simple yet practical question: given a new AI/ML model with high predictive power, how many labeled samples are needed to achieve a desired level of statistical power? We derive closed-form power formulas by characterizing the asymptotic variance of the PPI estimator and applying Wald test inversion to obtain the required labeled sample size. Our results cover widely used settings including two-sample comparisons and risk measures in 2x2 tables. We find that a useful rule of thumb is that the reduction in required labeled samples relative to classical designs scales roughly with the R2 between the predictions and the ground truth. Our analytical formulas are validated using Monte Carlo simulations, and we illustrate the framework in three contemporary biomedical applications spanning single-cell transcriptomics, clinical blood pressure measurement, and dermoscopy imaging. We provide our software as an R package and online calculators at https://github.com/yiqunchen/pppower.

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Large Language Models for Full-Text Methods Assessment: A Case Study on Mediation Analysis

Systematic reviews are crucial for synthesizing scientific evidence but remain labor-intensive, especially when extracting detailed methodological information. Large language models (LLMs) offer potential for automating methodological assessments, promising to transform evidence synthesis. Here, using causal mediation analysis as a representative methodological domain, we benchmarked state-of-the-art LLMs against expert human reviewers across 180 full-text scientific articles. Model performance closely correlated with human judgments (accuracy correlation 0.71; F1 correlation 0.97), achieving near-human accuracy on straightforward, explicitly stated methodological criteria. However, accuracy sharply declined on complex, inference-intensive assessments, lagging expert reviewers by up to 15%. Errors commonly resulted from superficial linguistic cues -- for instance, models frequently misinterpreted keywords like "longitudinal" or "sensitivity" as automatic evidence of rigorous methodological approache, leading to systematic misclassifications. Longer documents yielded lower model accuracy, whereas publication year showed no significant effect. Our findings highlight an important pattern for practitioners using LLMs for methods review and synthesis from full texts: current LLMs excel at identifying explicit methodological features but require human oversight for nuanced interpretations. Integrating automated information extraction with targeted expert review thus provides a promising approach to enhance efficiency and methodological rigor in evidence synthesis across diverse scientific fields.

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LAVA: Language Model Assisted Verbal Autopsy for Cause-of-Death Determination

Verbal autopsy (VA) is a critical tool for estimating causes of death in resource-limited settings where medical certification is unavailable. This study presents LA-VA, a proof-of-concept pipeline that combines Large Language Models (LLMs) with traditional algorithmic approaches and embedding-based classification for improved cause-of-death prediction. Using the Population Health Metrics Research Consortium (PHMRC) dataset across three age categories (Adult: 7,580; Child: 1,960; Neonate: 2,438), we evaluate multiple approaches: GPT-5 predictions, LCVA baseline, text embeddings, and meta-learner ensembles. Our results demonstrate that GPT-5 achieves the highest individual performance with average test site accuracies of 48.6% (Adult), 50.5% (Child), and 53.5% (Neonate), outperforming traditional statistical machine learning baselines by 5-10%. Our findings suggest that simple off-the-shelf LLM-assisted approaches could substantially improve verbal autopsy accuracy, with important implications for global health surveillance in low-resource settings.

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Testing for a difference in means of a single feature after clustering

For many applications, it is critical to interpret and validate groups of observations obtained via clustering. A common validation approach involves testing differences in feature means between observations in two estimated clusters. In this setting, classical hypothesis tests lead to an inflated Type I error rate. To overcome this problem, we propose a new test for the difference in means in a single feature between a pair of clusters obtained using hierarchical or $k$-means clustering. The test based on the proposed $p$-value controls the selective Type I error rate in finite samples and can be efficiently computed. We further illustrate the validity and power of our proposal in simulation and demonstrate its use on single-cell RNA-sequencing data.

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Selective inference for k-means clustering

We consider the problem of testing for a difference in means between clusters of observations identified via k-means clustering. In this setting, classical hypothesis tests lead to an inflated Type I error rate. To overcome this problem, we take a selective inference approach. We propose a finite-sample p-value that controls the selective Type I error for a test of the difference in means between a pair of clusters obtained using k-means clustering, and show that it can be efficiently computed. We apply our proposal in simulation, and on hand-written digits data and single-cell RNA-sequencing data.

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More powerful selective inference for the graph fused lasso

The graph fused lasso -- which includes as a special case the one-dimensional fused lasso -- is widely used to reconstruct signals that are piecewise constant on a graph, meaning that nodes connected by an edge tend to have identical values. We consider testing for a difference in the means of two connected components estimated using the graph fused lasso. A naive procedure such as a z-test for a difference in means will not control the selective Type I error, since the hypothesis that we are testing is itself a function of the data. In this work, we propose a new test for this task that controls the selective Type I error, and conditions on less information than existing approaches, leading to substantially higher power. We illustrate our approach in simulation and on datasets of drug overdose death rates and teenage birth rates in the contiguous United States. Our approach yields more discoveries on both datasets.

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Quantifying uncertainty in spikes estimated from calcium imaging data

In recent years, a number of methods have been proposed to estimate the times at which a neuron spikes on the basis of calcium imaging data. However, quantifying the uncertainty associated with these estimated spikes remains an open problem. We consider a simple and well-studied model for calcium imaging data, which states that calcium decays exponentially in the absence of a spike, and instantaneously increases when a spike occurs. We wish to test the null hypothesis that the neuron did not spike -- i.e., that there was no increase in calcium -- at a particular timepoint at which a spike was estimated. In this setting, classical hypothesis tests lead to inflated Type I error, because the spike was estimated on the same data used for testing. To overcome this problem, we propose a selective inference approach. We describe an efficient algorithm to compute finite-sample p-values that control selective Type I error, and confidence intervals with correct selective coverage, for spikes estimated using a recent proposal from the literature. We apply our proposal in simulation and on calcium imaging data from the spikefinder challenge.

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