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Hu Bin

Publications and source records attributed to Hu Bin.

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TUNeS: Neural Emulation of Large-Scale Structure Across Redshifts

In this work, we introduce TUNeS (Temporal UNet emulator for Structure formation), a neural network framework for accelerating N-body simulations by predicting the nonlinear evolution of the matter density field from an initial particle distribution. TUNeS employs a two-stage modeling strategy, combining particle-based inference with a density-field refinement on a regular grid, enabling accurate reconstruction of both large- and small-scale structures. The model is designed to operate across redshift, taking particle snapshots at arbitrary input redshifts and predicting density fields at arbitrary target redshifts. In this work, we evaluate its performance using simulations initialized at $z=100$, with predictions generated at multiple lower redshifts. Trained on only eight N-body simulations, TUNeS reproduces reference results with good agreement in both Gaussian and non-Gaussian statistics, including two-point correlations, one-point distributions, peak counts, and three-dimensional Minkowski functionals. In particular, at $k \simeq 1\,h\,\mathrm{Mpc}^{-1}$, the power spectrum error remains at the few-percent level. End-to-end inference from $256^3$ particles to a $256^3$ density grid can be completed in $\sim25\,\mathrm{second}$ on a single GPU. Thanks to its architectural design, the model naturally scales to larger particle numbers and larger volumes through particle batching and window-based refinement.

astro-ph.CO

OCELOT 2023: Cell Detection from Cell-Tissue Interaction Challenge

Pathologists routinely alternate between different magnifications when examining Whole-Slide Images, allowing them to evaluate both broad tissue morphology and intricate cellular details to form comprehensive diagnoses. However, existing deep learning-based cell detection models struggle to replicate these behaviors and learn the interdependent semantics between structures at different magnifications. A key barrier in the field is the lack of datasets with multi-scale overlapping cell and tissue annotations. The OCELOT 2023 challenge was initiated to gather insights from the community to validate the hypothesis that understanding cell and tissue (cell-tissue) interactions is crucial for achieving human-level performance, and to accelerate the research in this field. The challenge dataset includes overlapping cell detection and tissue segmentation annotations from six organs, comprising 673 pairs sourced from 306 The Cancer Genome Atlas (TCGA) Whole-Slide Images with hematoxylin and eosin staining, divided into training, validation, and test subsets. Participants presented models that significantly enhanced the understanding of cell-tissue relationships. Top entries achieved up to a 7.99 increase in F1-score on the test set compared to the baseline cell-only model that did not incorporate cell-tissue relationships. This is a substantial improvement in performance over traditional cell-only detection methods, demonstrating the need for incorporating multi-scale semantics into the models. This paper provides a comparative analysis of the methods used by participants, highlighting innovative strategies implemented in the OCELOT 2023 challenge.

cs.CV