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Changjun Li

Publications and source records attributed to Changjun Li.

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ScalePredictor: Instance-aware Scale Learning for Accurate Quantization of Vision Transformers

Vision Transformers have achieved remarkable success in many fields, yet their deployment on edge devices remains challenging due to their substantial computational demands. Post-Training Quantization (PTQ) offers an attractive solution by compressing models using a small calibration set with minimal training overhead. However, most existing PTQ works adopt a static quantization paradigm that is uniformly applied to all instances. Given the substantial diversity of natural images, the activation distributions vary significantly across samples, making these methods inherently suboptimal. In this paper, we propose ScalePredictor, a dynamic quantization framework for accurate and efficient quantization scale learning of ViTs. We first reveal a hidden correlation between the distribution range of shallow-layer activations and the optimal scales of deeper layers. Based on this, we develop a scale learning mechanism that integrates an efficient range extraction approach to capture robust range statistics at the shallow stage, which are then fed into a Taylor-motivated polynomial scale projection module to generate all quantization scales simultaneously. With the efficiency of polynomial approximation, ScalePredictor introduces insignificant computational overhead while avoiding costly just-in-time calibration. Extensive experiments on ImageNet demonstrate that ScalePredictor consistently outperforms prior PTQ methods, achieving a more favorable accuracy-efficiency trade-off. Code and additional results are shown in the supplementary materials.

cs.CV

Leveraging machine learning to estimate individualized treatment effects in cluster-randomized trials

Cluster-randomized trials (CRTs) are widely used to evaluate interventions delivered at the clinic, practice, or community level. Although standard analyses typically target average treatment effects, such summaries mask potentially meaningful variation in treatment response across individuals and clusters. This work addresses the estimation of conditional average treatment effects (CATEs) for continuous outcomes in two-arm parallel CRTs by defining causal estimands that incorporate both individual- and cluster-level baseline covariates while marginalizing over unobserved cluster heterogeneity. To estimate these quantities, we develop a unified framework based on mixed-effects machine learning, integrating and extending a range of existing approaches, including Bayesian additive regression trees with random effects, multilevel Bayesian causal forests, mixed-effects random forests, several mixed-effects gradient boosting procedures, and generalized additive mixed models, while incorporating cluster-specific random intercepts to account for within-cluster dependence. We evaluate these methods across diverse simulation scenarios and demonstrate their use in the Task Shifting and Blood Pressure Control in Ghana CRT, which investigates strategies for improving hypertension management. Drawing on these investigations, we provide practical guidance for applying mixed-effects machine learning to quantify treatment-effect heterogeneity in CRTs, together with reproducible code that enables investigators to implement all methods within a coherent workflow.

stat.ME

Improve Power of Knockoffs with Annotation Information of Covariates

Genome-wide association studies (GWAS) often find association signals between many genetic variants and traits of interest in a genomic region. Functional annotations of these variants provide valuable prior information that helps prioritize biologically relevant variants and enhances the power to detect causal variants. However, due to substantial correlations among these variants, a critical question is how to rigorously control the false discovery rate while effectively leveraging prior knowledge. We introduce annotation-informed knockoffs (AnnoKn), a knockoff-based method that performs annotation-informed variable selection with strict control of the false discovery rate. AnnoKn integrates the knockoff procedure with adaptive Lasso regression to evaluate the importance of multiple covariates while incorporating functional annotation information within a unified Bayesian framework. To facilitate real-world applications where individual-level data are not accessible, we further extend AnnoKn to operate on summary statistics. Through simulations and real-world applications to GTEx and GWAS datasets, we show that AnnoKn achieves superior power in detecting causal genetic variants compared with existing annotation-informed variable selection methods, while maintaining valid control over false discoveries.

stat.ME

Uncovering Treatment Effect Heterogeneity in Pragmatic Gerontology Trials

Detecting heterogeneity in treatment response enriches the interpretation of gerontologic trials. In aging research, estimating the effect of the intervention on clinically meaningful outcomes faces analytical challenges when it is truncated by death. For example, in the Whole Systems Demonstrator trial, a large cluster-randomized study evaluating telecare among older adults, the overall effect of the intervention on quality of life was found to be null. However, this marginal intervention estimate obscures potential heterogeneity of individuals responding to the intervention, particularly among those who survive to the end of follow-up. To explore this heterogeneity, we adopt a causal framework grounded in principal stratification, targeting the Survivor Average Causal Effect (SACE)-the treatment effect among "always-survivors," or those who would survive regardless of treatment assignment. We extend this framework using Bayesian Additive Regression Trees (BART), a nonparametric machine learning method, to flexibly model both latent principal strata and stratum-specific potential outcomes. This enables the estimation of the Conditional SACE (CSACE), allowing us to uncover variation in treatment effects across subgroups defined by baseline characteristics. Our analysis reveals that despite the null average effect, some subgroups experience distinct quality of life benefits (or lack thereof) from telecare, highlighting opportunities for more personalized intervention strategies. This study demonstrates how embedding machine learning methods, such as BART, within a principled causal inference framework can offer deeper insights into trial data with complex features including truncation by death and clustering-key considerations in analyzing pragmatic gerontology trials.

stat.AP

Pack-PTQ: Advancing Post-training Quantization of Neural Networks by Pack-wise Reconstruction

Post-training quantization (PTQ) has evolved as a prominent solution for compressing complex models, which advocates a small calibration dataset and avoids end-to-end retraining. However, most existing PTQ methods employ block-wise reconstruction, which neglects cross-block dependency and exhibits a notable accuracy drop in low-bit cases. To address these limitations, this paper presents a novel PTQ method, dubbed Pack-PTQ. First, we design a Hessian-guided adaptive packing mechanism to partition blocks into non-overlapping packs, which serve as the base unit for reconstruction, thereby preserving the cross-block dependency and enabling accurate quantization parameters estimation. Second, based on the pack configuration, we propose a mixed-precision quantization approach to assign varied bit-widths to packs according to their distinct sensitivities, thereby further enhancing performance. Extensive experiments on 2D image and 3D point cloud classification tasks, using various network architectures, demonstrate the superiority of our method over the state-of-the-art PTQ methods.

cs.CV