arXiv subjects

Apaar Sadhwani

Publications and source records attributed to Apaar Sadhwani.

6 recordsLinked to original sources

arXiv2026

AugLift: Depth-Aware Input Reparameterization Improves Domain Generalization in 2D-to-3D Pose Lifting

Lifting-based 3D human pose estimation infers 3D joints from 2D keypoints but generalizes poorly because $(x,y)$ coordinates alone are an ill-posed, sparse representation that discards geometric information modern foundation models can recover. We propose \emph{AugLift}, which changes the representation format of lifting from 2D coordinates to a 6D geometric descriptor via two modules: (1) an \emph{Uncertainty-Aware Depth Descriptor} (UADD) -- a compact tuple $(c, d, d_{\min}, d_{\max})$ extracted from a confidence-scaled neighborhood of an off-the-shelf monocular depth map -- and (2) a scale normalization component that handles train/test distance shifts. AugLift requires no new sensors, no new data collection, and no architectural changes beyond widening the input layer; because it operates at the representation level, it is composable with any lifting architecture or domain generalization technique. In the detection setting, AugLift reduces cross-dataset MPJPE by $10.1$% on average across four datasets and four lifting architectures while improving in-distribution accuracy by $4.0$%; post-hoc analysis shows gains concentrate on novel poses and occluded joints. In the ground-truth 2D setting, combining AugLift with PoseAug's differentiable domain generalization achieves state-of-the-art cross-dataset performance ($62.4$\,mm on 3DHP, $92.6$\,mm on 3DPW; $14.5$% and $22.2$% over PoseAug), demonstrating that foundation-model depth provides genuine geometric signal complementary to explicit 3D augmentation. Code will be made publicly available.

cs.CV↗

arXiv2026

MoCHA: Denoising Caption Supervision for Motion-Text Retrieval

Text-motion retrieval systems learn shared embedding spaces from motion-caption pairs via contrastive objectives. However, each caption is not a deterministic label but a sample from a distribution of valid descriptions: different annotators produce different text for the same motion, mixing motion-recoverable semantics (action type, body parts, directionality) with annotator-specific style and inferred context that cannot be determined from 3D joint coordinates alone. Standard contrastive training treats each caption as the single positive target, overlooking this distributional structure and inducing within-motion embedding variance that weakens alignment. We propose MoCHA, a text canonicalization framework that reduces this variance by projecting each caption onto its motion-recoverable content prior to encoding, producing tighter positive clusters and better-separated embeddings. Canonicalization is a general principle: even deterministic rule-based methods improve cross-dataset transfer, though learned canonicalizers provide substantially larger gains. We present two learned variants: an LLM-based approach (GPT-5.2) and a distilled FlanT5 model requiring no LLM at inference time. MoCHA operates as a preprocessing step compatible with any retrieval architecture. Applied to MoPa (MotionPatches), MoCHA sets a new state of the art on both HumanML3D (H) and KIT-ML (K): the LLM variant achieves 13.9% T2M R@1 on H (+3.1pp) and 24.3% on K (+10.3pp), while the LLM-free T5 variant achieves gains of +2.5pp and +8.1pp. Canonicalization reduces within-motion text-embedding variance by 11-19% and improves cross-dataset transfer substantially, with H to K improving by 94% and K to H by 52%, demonstrating that standardizing the language space yields more transferable motion-language representations.

cs.CV↗

arXiv2025

A Set-Sequence Model for Time Series

Many prediction problems across science and engineering, especially in finance and economics, involve large cross-sections of individual time series, where each unit (e.g., a loan, stock, or customer) is driven by unit-level features and latent cross-sectional dynamics. While sequence models have advanced per-unit temporal prediction, capturing cross-sectional effects often still relies on hand-crafted summary features. We propose Set-Sequence, a model that learns cross-sectional structure directly, enhancing expressivity and eliminating manual feature engineering. At each time step, a permutation-invariant Set module summarizes the unit set; a Sequence module then models each unit's dynamics conditioned on both its features and the learned summary. The architecture accommodates unaligned series, supports varying numbers of units at inference, integrates with standard sequence backbones (e.g., Transformers), and scales linearly in cross-sectional size. Across a synthetic contagion task and two large-scale real-world applications, equity portfolio optimization and loan risk prediction, Set-Sequence significantly outperforms strong baselines, delivering higher Sharpe ratios, improved AUCs, and interpretable cross-sectional summaries.

cs.LG↗

arXiv2020

Interpretable Survival Prediction for Colorectal Cancer using Deep Learning

Deriving interpretable prognostic features from deep-learning-based prognostic histopathology models remains a challenge. In this study, we developed a deep learning system (DLS) for predicting disease specific survival for stage II and III colorectal cancer using 3,652 cases (27,300 slides). When evaluated on two validation datasets containing 1,239 cases (9,340 slides) and 738 cases (7,140 slides) respectively, the DLS achieved a 5-year disease-specific survival AUC of 0.70 (95%CI 0.66-0.73) and 0.69 (95%CI 0.64-0.72), and added significant predictive value to a set of 9 clinicopathologic features. To interpret the DLS, we explored the ability of different human-interpretable features to explain the variance in DLS scores. We observed that clinicopathologic features such as T-category, N-category, and grade explained a small fraction of the variance in DLS scores (R2=18% in both validation sets). Next, we generated human-interpretable histologic features by clustering embeddings from a deep-learning based image-similarity model and showed that they explain the majority of the variance (R2 of 73% to 80%). Furthermore, the clustering-derived feature most strongly associated with high DLS scores was also highly prognostic in isolation. With a distinct visual appearance (poorly differentiated tumor cell clusters adjacent to adipose tissue), this feature was identified by annotators with 87.0-95.5% accuracy. Our approach can be used to explain predictions from a prognostic deep learning model and uncover potentially-novel prognostic features that can be reliably identified by people for future validation studies.

eess.IV↗

arXiv2019

Deep learning-based survival prediction for multiple cancer types using histopathology images

Prognostic information at diagnosis has important implications for cancer treatment and monitoring. Although cancer staging, histopathological assessment, molecular features, and clinical variables can provide useful prognostic insights, improving risk stratification remains an active research area. We developed a deep learning system (DLS) to predict disease specific survival across 10 cancer types from The Cancer Genome Atlas (TCGA). We used a weakly-supervised approach without pixel-level annotations, and tested three different survival loss functions. The DLS was developed using 9,086 slides from 3,664 cases and evaluated using 3,009 slides from 1,216 cases. In multivariable Cox regression analysis of the combined cohort including all 10 cancers, the DLS was significantly associated with disease specific survival (hazard ratio of 1.58, 95% CI 1.28-1.70, p<0.0001) after adjusting for cancer type, stage, age, and sex. In a per-cancer adjusted subanalysis, the DLS remained a significant predictor of survival in 5 of 10 cancer types. Compared to a baseline model including stage, age, and sex, the c-index of the model demonstrated an absolute 3.7% improvement (95% CI 1.0-6.5) in the combined cohort. Additionally, our models stratified patients within individual cancer stages, particularly stage II (p=0.025) and stage III (p<0.001). By developing and evaluating prognostic models across multiple cancer types, this work represents one of the most comprehensive studies exploring the direct prediction of clinical outcomes using deep learning and histopathology images. Our analysis demonstrates the potential for this approach to provide prognostic information in multiple cancer types, and even within specific pathologic stages. However, given the relatively small number of clinical events, we observed wide confidence intervals, suggesting that future work will benefit from larger datasets.

q-bio.QM↗

arXiv2018

Deep Learning for Mortgage Risk

We develop a deep learning model of multi-period mortgage risk and use it to analyze an unprecedented dataset of origination and monthly performance records for over 120 million mortgages originated across the US between 1995 and 2014. Our estimators of term structures of conditional probabilities of prepayment, foreclosure and various states of delinquency incorporate the dynamics of a large number of loan-specific as well as macroeconomic variables down to the zip-code level. The estimators uncover the highly nonlinear nature of the relationship between the variables and borrower behavior, especially prepayment. They also highlight the effects of local economic conditions on borrower behavior. State unemployment has the greatest explanatory power among all variables, offering strong evidence of the tight connection between housing finance markets and the macroeconomy. The sensitivity of a borrower to changes in unemployment strongly depends upon current unemployment. It also significantly varies across the entire borrower population, which highlights the interaction of unemployment and many other variables. These findings have important implications for mortgage-backed security investors, rating agencies, and housing finance policymakers.

q-fin.ST↗