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# Survival analysis

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  1. arXiv

    Mouse tumor drug screens need not be run in full: GrAFT-PDX couples growth and death in one model and can stop losing combinations early

    Patient-derived xenografts (PDX) implant human tumors into immunocompromised mice to test drugs, but screening every tumor-drug combination is infeasible in time and cost. GrAFT-PDX is a Bayesian model that jointly models tumor growth trajectories and mouse death risk, using a low-rank tensor decomposition to share information across PDX lines, treatments and time, so it can impute untested experiments and predict death times. On the large PDXe screen it assigns higher log probability to death times than Royston-Parmar and other survival baselines, matches strong baselines on tumor response, and preserves known gene-drug associations without genomic input.

  2. bioRxiv

    A snapshot can rank a mouse's age: within-session ordering hits 65%, and mice that look older are frailer with 14% higher death hazard

    A laboratory mouse's age can be read from an ordinary photograph, but what transfers is relative age rather than absolute age. Across 2,846 photographs of 1,292 mice from seven facilities, a frozen DINOv2 vision model with ridge regression predicted age; on unseen facilities the median absolute error was 138 days, yet within a session the older of two mice was ranked older in 65% of pairs, rising above 95% for age gaps over 500 days. Mice predicted older than their age were frailer, with each 100 days of photographic age gap linked to 0.12 SD more frailty and a 14% higher hazard of death.

  3. arXiv

    One H&E slide, three transcriptomes: a multi-scale graph network beats DeepSpot2Cell in cell-level PCC and AUROC

    Spatial and single-cell transcriptomics reveal where genes are expressed in tissue, but each slide is expensive and scarce, while routine H&E whole-slide images are abundant. A multi-scale graph neural network trains on TCGA bulk data, Visium spatial data and Xenium single-cell data together, using consistency losses to keep predictions aligned across the three scales, and predicts bulk, spatial and single-cell expression directly from slide images. It performs best at slide level and moderately at patch level, with single-cell prediction the hardest; on Xenium its cell-level PCC and AUROC exceed DeepSpot2Cell, while DeepSpot2Cell leads at patch level.

  4. Nankai University team's 362-day Internet-wide scan finds exposed Ollama endpoints grew 53.3% in a year while only 0.43%–2.90% of below-fix IPs upgraded in place

    Using XMap to probe port 11434 across the full IPv4 space daily from 2025-02-14 to 2026-02-13 over 362 observed days, a Nankai University team found 152,137 cumulative exposed Ollama endpoints, with daily alive endpoints rising from 10,473 to 16,059 (+53.3%), 26.4% of IPs appearing on a single day, only 0.43%–2.90% of below-fix IPs upgrading in place across five CVE cutoffs, the top five countries/regions holding about 70% of weighted observations, and the top five ASNs all cloud or hosting providers, complemented by PTR and port-443 TLS probing of operational characteristics.

  5. arXiv

    Across 14 event logs, remaining-time error and uncertainty rise with delay, and uncertainty features lift average delay-detection recall from 0.21 to 0.61

    Analyzing the intrinsic difficulty of delay detection across 14 public event logs, the study finds that remaining times are strongly right-skewed, that existing LSTM models capture the mode of the distribution but perform poorly on high-delay cases, and that prediction error and prediction-interval width both grow with true remaining time (positive in 10 of 14 logs); it then evaluates imbalanced regression approaches (SMOGN resampling, CSW, BMSE, EAL, SERA) with only limited benefit, and instead feeds uncertainty features from a survival model (prediction standard deviation, 80% and 90% prediction-interval widths, tail mass, and temporal context) into a CatBoost classifier for binary delay detection, raising average recall from 0.21 to 0.61 at the q=0.

  6. CleanSurvival uses reinforcement learning to auto-select preprocessing pipelines for survival analysis, improving predictive performance over simple baselines on real-world benchmarks

    The work presents CleanSurvival, a reinforcement-learning (Q-learning) based automated data-preprocessing framework tailored to time-to-event (survival analysis) models for censored data: it selects among combinations of data imputation, outlier detection, and feature extraction techniques to optimize performance for a Cox, random forest, neural network, or user-supplied time-to-event model; on real-world dataset benchmarks, this Q-learning-based preprocessing improved predictive performance relative to simple baselines, runtime behavior was condition-dependent and most clearly interpretable in the best-covered benchmark cells, and a simulation study showed effectiveness across different types and levels of missingness and noise.

  7. Benchmarking AI Vibe Coding for Clinical Statistical Analysis: A Structured Evaluation in Pulmonary Hypertension Research

    This study had five current large language models (GPT 5.3, Claude Sonnet 4.6, Gemini 2.5 Flash, Perplexity, and Grok) reproduce three statistical tasks from a published clinical workflow under identical datasets and standardised prompts—descriptive table generation, Kaplan–Meier survival analysis, and Cox proportional hazards modelling—and compared their outputs with analyses by two experts trained in mathematical statistics on grouping correctness, numerical accuracy, missing-value handling, and quality of generated R code, finding that all five models produced correct descriptive statistics once dataset variables were specified explicitly, that two models failed the initial descriptive benchmark because of variable-name ambiguity but recovered after prompt clarification, that all models

  8. Biparametric MRI Radiomics Combined with Serum Bone Turnover Biomarkers for Predicting Postoperative Bone Metastasis in Prostate Cancer: Precision Selection for Targeted Radionuclide Therapy

    In a prospective single-center cohort of 143 patients with clinically localized prostate cancer (cT1-2N0M0) undergoing laparoscopic radical prostatectomy, the study measured preoperative serum bone metabolism indicators such as osteocalcin N-terminal mid-fragment and alkaline phosphatase, extracted biparametric MRI radiomics variables including apparent diffusion coefficient mean and K trans mean, and integrated serum and imaging biomarkers with a multivariate logistic regression model; the integrated model reached an area under the ROC curve of 0.984, significantly outperforming individual biomarkers and imaging features (all p < 0.001), showed clinical net benefit with strong calibration (Hosmer-Lemeshow test p = 0.

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