跳到正文
研踪PaperTrail

论文库

检索计算机领域论文,按研究方向、作者或关键词筛选。

部分采集异常
正在读取账号与研究记录…

全站更新概况

+0新增论文
+0其中 AI 相关
+2已有论文修订
+100新增 AI 导读

arXiv 最近完成扫描:2026-11-15 01:33 · 全站最近入库:2026-11-14 15:09各信源进度 →

统计口径与数据新鲜度

统计 2026-11-14 02:33 — 2026-11-15 02:33(北京时间) · 点击数字查看对应简报;AI 相关包含在新增论文内。

最近完成检查:2026-11-15 01:33最近发现新增版本:2026-11-14 15:09库内论文最新更新时间:2026-11-13 02:59

每分钟刷新已保存的数据。空检查不代表采集异常;新收录可能包含历史论文。AI 导读按新增版本计数。

23,348 已收录论文19,580 AI 相关6,729 有修订112 HF 社区发现

浏览论文库

时间范围跟随排序:版本更新、本站收录或首次发表。最新收录可能包含历史论文。部分信源异常,查看状态 →

找到 2 篇论文 · 按版本更新时间排序上轮扫描起点 2026-11-15 01:32(北京时间)
新论文 · v1arXiv:2611.13070

IC-GNN: Modeling Individualized Brain Community Organization for Disease Prediction

Yang Zhang, Xiao Zhou, Jonathan Warrell, Avram Holmes, Xuan Zhang, Mark Gerstein, for the Alzheimer's Disease Neuroimaging Initiative

原文摘要

Brain networks exhibit modular organization, where community structures vary substantially across individuals and diseases. Understanding these individual differences is crucial for advancing both basic neuroscience research and precision medicine. However, widely used predefined group-level brain atlases often overlook this heterogeneity. While individualized functional parcellations capture subject-specific variability in community boundaries, they often require lengthy scan times to achieve fine-grained resolution and complicate cross-subject comparisons. To address this trade-off and investigate how individualized community organization captures disease-associated changes across individuals, we propose IC-GNN, an atlas-anchored model that forms distinct, individualized functional communities directly over atlas-defined brain regions. IC-GNN derives discrete, individualized multiscale communities from resting-state functional magnetic resonance imaging (fMRI) data, refines community-guided connections, and adapts shared regional weights to each subject's community context to enable both individualized modeling and group-level comparisons. Across more than 30,000 participants from ABIDE (autism spectrum disorder), ADNI (Alzheimer's disease), and the UK Biobank (depression), IC-GNN achieves the highest performance compared with 15 baseline methods. We further demonstrate that these individualized communities are reproducible within scans and across sessions, and carry predictive power on their own. Furthermore, IC-GNN identifies disease-related shifts in community organization that align with established literature, highlighting a promising approach for modeling individualized community structure for disease prediction and biomarker discovery.

cs.LG · q-bio.NC

新论文 · v1arXiv:2610.38648

Logical Guidance of Stochastic Interpolants

Gerrit Gerhartz, Francesco Alesiani, Jonathan Warrell, Henrik Christiansen, Matheus Ferraz, Mathias Niepert

原文摘要

Guidance and composition of generative models have applications in visual design, chemistry, and biology. Logical guidance composes conditional scores exactly for diffusion models. However, Flow Matching (FM) and Stochastic Interpolants (SI) learn velocity fields. We show that negation and exclusive disjunction admit exact conditional velocity composition on any interpolant, whereas conjunction, and therefore any formula containing one, is exact on Gaussian paths but in general incurs a drift-interaction error, so composed velocities need not sample the logical target. LOGSI solves this by using score-based re-equilibration as our principled mechanism and falling back to the Gaussian-path velocity rule as an approximate transport predictor. In non-Gaussian bridge problems, generation alternates transport steps with score re-equilibration steps. On image trans fer (EMNIST to CMNIST, CelebA) and QM9 source-to-target molecular editing with logical attribute constraints, LOGSI improves rule conformity at the same network-evaluation budget over composed-velocity baselines, while also improving fidelity on the image tasks. More broadly, LOGSI applies wherever stochastic interpolants need guidance and logical combinations of constraints are natural.

cs.LG