A DeepLabV3 segmentation model that separates tissue foreground from slide background in H&E and IHC whole-slide images, shipping as the tissue-detection step of the HEST-Library.
HEST Tissue Segmentation is a utility model that separates tissue foreground from slide background in whole-slide histopathology images. Whole-slide images (WSIs) are gigapixel scans in which most of the canvas is empty glass, so any downstream analysis first needs a reliable mask marking where tissue actually sits. This model provides that mask, producing a binary tissue-versus-background segmentation that lets a pipeline discard blank regions and extract patches only from informative areas.
The model was released as the automated tissue-detection step of the HEST-Library, the software toolkit accompanying HEST-1k — a collection of 1,229 spatial transcriptomic profiles paired with histology images spanning 153 cohorts, 26 organs, and 367 cancer samples. HEST-1k and its tooling were introduced by the Mahmood Lab at Harvard Medical School in the NeurIPS 2024 Spotlight paper "HEST-1k: A Dataset for Spatial Transcriptomics and Histology Image Analysis" (June 2024). Within that pipeline, the segmentation model runs before patching: it isolates tissue so that image patches can be cropped around each spatial transcriptomics spot for benchmarking and multimodal training.
This is a preprocessing utility rather than a general-purpose foundation model. It performs one narrow, reproducible job — foreground masking — and is best understood as infrastructure that supports the larger HEST benchmark and the histology foundation models evaluated on it, not as a representation learner in its own right.
segment_tissue
functionality, giving a one-call route to reproducible tissue masks inside the
broader HEST workflow.The model is a DeepLabV3 semantic segmentation network with an ImageNet-pretrained ResNet50 backbone, finetuned on annotated tissue regions drawn from HEST-1k and the Acrobat H&E/IHC registration dataset. DeepLabV3 uses atrous (dilated) convolutions to capture multi-scale context while preserving spatial resolution, which suits the large, texture-rich fields of a histology slide. The finetuned network outputs a tissue mask that the HEST-Library then uses to crop patches at a fixed magnification around each spatial transcriptomics spot; those patches feed the HEST-Benchmark and multimodal finetuning of histology foundation models. Training data and the model itself are distributed under the Attribution-NonCommercial-ShareAlike 4.0 International license (CC BY-NC-SA 4.0), the same license covering HEST-1k, the HEST-Library, and the HEST-Benchmark.
The model serves researchers assembling or analyzing spatial transcriptomics and computational pathology datasets. Its immediate use is preprocessing: masking tissue so that patch extraction, quality control, and stain-aware cropping run only on relevant slide regions. Because it handles both H&E and IHC, it fits pipelines that mix stain types, and it underpins the patching that supplies HEST-Benchmark tasks and multimodal training of histology encoders. Teams building their own WSI workflows can reuse it as a drop-in tissue detector rather than annotating masks or tuning heuristic thresholds by hand.
HEST Tissue Segmentation contributes to the reproducibility of the widely used HEST toolkit by standardizing how tissue is detected before downstream analysis, removing a common source of variation in histology pipelines. Its significance is practical rather than methodological: it packages a proven segmentation architecture into an accessible, pipeline-ready component that many groups can adopt directly. Its scope is deliberately narrow — it is a single-purpose preprocessing model, not a foundation model, and the non-commercial license limits industrial reuse. Like the rest of the HEST release, it is a research tool and has not been validated for clinical diagnostic use.
Jaume, G., et al. (2024) HEST-1k: A Dataset for Spatial Transcriptomics and Histology Image Analysis. Neural Information Processing Systems.
DOI: 10.48550/arXiv.2406.16192Papers that recently cited this model.
Yuhang Yang, Yong Bu, S. Zhou, et al.
Jul 2026
Qiqi Lu, Qianjin Feng, Shaoqun Zeng, et al.
Jun 2026
Gbègninougbo Aurel Davy Tchokponhoue, Sevda Ougut, Ali Idri, et al.
Jun 2026
The most-cited papers that cite this model.
Eric Zimmermann, E. Vorontsov, Julian Viret, et al.
arXiv.org · Aug 2024
Marija Pizurica, Yuanning Zheng, F. Carrillo-Perez, et al.
Nature Communications · Nov 2024
Tong Ding, Sophia J. Wagner, Andrew H. Song, et al.
Nature Medicine · Nov 2025
D. Komura, M. Ochi, S. Ishikawa
Computational and Structural Biotechnology Journal · Dec 2024
Guillaume Jaume, Anurag Vaidya, Andrew Zhang, et al.
European Conference on Computer Vision · Aug 2024
Share of papers citing this model.