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Yushi Liu

Publications and source records attributed to Yushi Liu.

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Empirical Simulation of Survival and Mixed-Type Data for Clinical Trial Design

Simulating realistic time-to-event data is essential for planning and evaluating complex clinical trial designs. Conventional approaches often sample event times from parametric families, such as Weibull or log-normal distributions, which restrict hazard shapes and may poorly represent observed survival data. We propose an empirical copula-based framework for simulating multivariate data containing continuous, binary, count, and right-censored time-to-event variables. The method completes censored historical survival data using a two-zone procedure that combines conditional Kaplan-Meier imputation with a parametric tail. It matches a target survival distribution through a log-scale location-scale transformation and a power distortion of the empirical percentile function, while preserving historical dependence through a Gaussian copula fitted to rank correlations. In an oncology trial of previously treated non-small-cell lung cancer, the method reconstructs overall survival and progression-free survival curves for the experimental arm using control-arm data and a small set of target percentiles. Simulations preserve rank correlations among baseline covariates and the dependence between progression-free and overall survival, with censored Kendall's tau of 0.522 compared with 0.549 in the observed data. The method is implemented in the R package EmpiricalSim.

stat.ME

PostureObjectstitch: Anomaly Image Generation Considering Assembly Relationships in Industrial Scenarios

Image generation technology can synthesize condition-specific images to supplement real-world industrial anomaly data and enhance anomaly detection model performance. Existing generation techniques rarely account for the pose and orientation of industrial components in assembly, making the generated images difficult to utilize for downstream application. To solve this, we propose a novel image synthesis approach, called PostureObjectStitch, that achieves accurate generation to meet the requirement of industrial assembly. A condition decoupling approach is introduced to separate input multi-view images into high-frequency, texture, and RGB features. The feature temporal modulation mechanism adapts these features across diffusion model time-steps, enabling progressive generation from coarse to fine details while maintaining consistency. To ensure semantic accuracy, we introduce a conditional loss that enhances critical industrial elements and a geometric prior that guides component positioning for correct assembly relationships. Comprehensive experimental results on the MureCom dataset, our newly contributed DreamAssembly dataset, and the downstream application validate the outstanding performance of our method.

cs.CV

ETZ: A Modeling Principle for Confirmability of Drug-Development Studies

Transitioning from Phase 2 to Phase 3 in drug development, at a rate of $\approx$40%, is the most stringent among phase transitions (Hay et al. (2014)). Yet, success rate at Phase 3 leading to approval is only $\approx$50% (Arrowsmith (2011b)). To improve Confirmability, we propose a methodological shift: replacing multiple hypothesis testing with inference based on confidence sets, and substituting conventional power and sample size calculations with a Confidently Bounded Quantile (CBQ) framework. Our confidence set inferences to answer the questions of whether to transition to a Confirmatory study as well as what to designate as the endpoint in that study. Construction of our directed confidence sets follows the Partitioning Principle, taking the best of each of Pivoting and Neyman Confidence Set Construction. Rooted in Tukey's Confidently Bounded Allowance (CBA) (Tukey (1994a)), our proposed CBQ makes the transitioning decision following the Correct and Useful Inference principle in Hsu (1996). CBQ removes from "power" the probability of rejecting for wrong reasons, eliminating the need for informal discounting in power calculation that has existed in the biopharmaceutical industry. ETZ, the modeling principle proposed in Wang et al. (2025), quantifies the impact of three variability components on confirmability. In repeated-measures RCTs, it separates within-subject and between-subject variability, further dividing the latter into baseline and trajectory components. This enables informed investment decisions for the sponsors on targeting variability reduction to improve confirmability. A Shiny-based Confirmability App supports all computations.

stat.ME

Counterfactual Uncertainty Quantification of Factual Estimand of Efficacy from Before-and-After Treatment Repeated Measures Randomized Controlled Trials

This article quantifies the uncertainty reduction achievable for \textit{counterfactual} estimand, and cautions against potential bias when the estimand uses Digital Twins. Posed by Neyman (1923a) who showed unbiased \textit{point estimation} from designed \textit{factual} experiments is possible, \textit{counterfactual} uncertainty quantification (CUQ) remained an open challenge for about one hundred years. The $Rx: C$ \textit{counterfactual} efficacy we focus on is the ideal estimand for comparing treatment $Rx$ with control $C$, the expected outcome differential if each patient received \textit{both} $Rx$ and $C$. Enabled by our new statistical modeling principle called ETZ, we show CUQ is achievable in Randomized Controlled Trials (RCTs) with \textit{Before-and-After} Repeated Measures, common in many therapeutic areas. The CUQ we are able to achieve typically has lower variability than factual UQ. We caution against using predictors with measurement error, which violates regression assumptions and can cause \textit{attenuation} bias in estimating treatment effects. For traditional medicine and population-averaged targeted therapy, counterfactual point estimation remains unbiased. However, in both Real Human and Digital Twin approaches, estimating effects in \emph{subgroups} may suffer attenuation bias.

stat.ML

Efficient End-to-End Detection of 6-DoF Grasps for Robotic Bin Picking

Bin picking is an important building block for many robotic systems, in logistics, production or in household use-cases. In recent years, machine learning methods for the prediction of 6-DoF grasps on diverse and unknown objects have shown promising progress. However, existing approaches only consider a single ground truth grasp orientation at a grasp location during training and therefore can only predict limited grasp orientations which leads to a reduced number of feasible grasps in bin picking with restricted reachability. In this paper, we propose a novel approach for learning dense and diverse 6-DoF grasps for parallel-jaw grippers in robotic bin picking. We introduce a parameterized grasp distribution model based on Power-Spherical distributions that enables a training based on all possible ground truth samples. Thereby, we also consider the grasp uncertainty enhancing the model's robustness to noisy inputs. As a result, given a single top-down view depth image, our model can generate diverse grasps with multiple collision-free grasp orientations. Experimental evaluations in simulation and on a real robotic bin picking setup demonstrate the model's ability to generalize across various object categories achieving an object clearing rate of around $90 \%$ in simulation and real-world experiments. We also outperform state of the art approaches. Moreover, the proposed approach exhibits its usability in real robot experiments without any refinement steps, even when only trained on a synthetic dataset, due to the probabilistic grasp distribution modeling.

cs.RO

A fusion learning method to subgroup analysis of Alzheimer's disease

Uncovering the heterogeneity in the disease progression of Alzheimer's is a key factor to disease understanding and treatment development, so that interventions can be tailored to target the subgroups that will benefit most from the treatment, which is an important goal of precision medicine. However, in practice, one top methodological challenge hindering the heterogeneity investigation is that the true subgroup membership of each individual is often unknown. In this article, we aim to identify latent subgroups of individuals who share a common disorder progress over time, to predict latent subgroup memberships, and to estimate and infer the heterogeneous trajectories among the subgroups. To achieve these goals, we apply a concave fusion learning method proposed in Ma and Huang (2017) and Ma et al. (2019) to conduct subgroup analysis for longitudinal trajectories of the Alzheimer's disease data. The heterogeneous trajectories are represented by subject-specific unknown functions which are approximated by B-splines. The concave fusion method can simultaneously estimate the spline coefficients and merge them together for the subjects belonging to the same subgroup to automatically identify subgroups and recover the heterogeneous trajectories. The resulting estimator of the disease trajectory of each subgroup is supported by an asymptotic distribution. It provides a sound theoretical basis for further conducting statistical inference in subgroup analysis..

stat.ME