B16BL6: A public time-lapse microscopy dataset and data-centric annotation pipeline for cell and division detection

Automated cell detection and identification of mitotic division events in phase-contrast microscopy are essential for quantifying proliferation, phenotypic response, and population dynamics, yet practical deployment remains limited by annotation cost and unclear architecture selection under real-time constraints. This paper releases B16BL6, a public phase-contrast time-lapse microscopy dataset comprising 1800 frames (1600 × 1200) with 93,637 bounding-box annotations for two classes (Cell and Division). To enable scalable labeling at this density, we present a three-stage annotation pipeline that combines (i) expert manual labeling of a representative subset, (ii) YOLO-based pseudo-label generation with expert refinement, and (iii) temporally consistent label propagation using a detector–tracker hybrid with an enhanced DeepSORT variant. Using this dataset, we benchmark seven contemporary detectors spanning one-stage CNNs (YOLOv8x, YOLOv11-L, SSD300/512), two-stage models (Faster R-CNN, Mask R-CNN, Libra R-CNN), and a real-time transformer (RT-DETR-L). Evaluation is multi-dimensional, covering detection accuracy ([email protected] and [email protected]:0.95), class-specific AP, inference speed, parameter/GFLOP complexity, and imbalance sensitivity via the Cell-Division AP gap, together with a supplementary heuristic efficiency score for deployment-oriented comparison. Results show that YOLOv8x achieves the best accuracy ([email protected] = 0.837), YOLOv11-L provides the best accuracy–speed balance (20.15 FPS, [email protected] = 0.811), and two-stage detectors exhibit more stable class-level performance under imbalance, while SSD offers maximal throughput at reduced precision. Rather than proposing a new detection architecture, this work releases a densely annotated microscopy dataset, a scalable annotation workflow, and a unified benchmark of modern detectors, providing practical guidance for scalable microscopy pipelines and downstream tracking and division analysis.

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Publication Details

Journal
Array
Published
2026-05-29
DOI
https://doi.org/10.1016/j.array.2026.100946
Primary Topic
Cell Image Analysis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

B16BL6: A public time-lapse microscopy dataset and data-centric annotation pipeline for cell and division detection

Mokhaled N. A. Al-Hamadani, Balázs Harangi, András Hajdú, Péter Szilágyi et al.
Array
Cell Image Analysis Techniques
article

B16BL6: A public time-lapse microscopy dataset and data-centric annotation pipeline for cell and division detection

Mokhaled N. A. Al-Hamadani, Balázs Harangi, András Hajdú, Péter Szilágyi, Gabor Szeman-Nagy
article en

Abstract

Automated cell detection and identification of mitotic division events in phase-contrast microscopy are essential for quantifying proliferation, phenotypic response, and population dynamics, yet practical deployment remains limited by annotation cost and unclear architecture selection under real-time constraints. This paper releases B16BL6, a public phase-contrast time-lapse microscopy dataset comprising 1800 frames (1600 × 1200) with 93,637 bounding-box annotations for two classes (Cell and Division). To enable scalable labeling at this density, we present a three-stage annotation pipeline that combines (i) expert manual labeling of a representative subset, (ii) YOLO-based pseudo-label generation with expert refinement, and (iii) temporally consistent label propagation using a detector–tracker hybrid with an enhanced DeepSORT variant. Using this dataset, we benchmark seven contemporary detectors spanning one-stage CNNs (YOLOv8x, YOLOv11-L, SSD300/512), two-stage models (Faster R-CNN, Mask R-CNN, Libra R-CNN), and a real-time transformer (RT-DETR-L). Evaluation is multi-dimensional, covering detection accuracy ([email protected] and [email protected]:0.95), class-specific AP, inference speed, parameter/GFLOP complexity, and imbalance sensitivity via the Cell-Division AP gap, together with a supplementary heuristic efficiency score for deployment-oriented comparison. Results show that YOLOv8x achieves the best accuracy ([email protected] = 0.837), YOLOv11-L provides the best accuracy–speed balance (20.15 FPS, [email protected] = 0.811), and two-stage detectors exhibit more stable class-level performance under imbalance, while SSD offers maximal throughput at reduced precision. Rather than proposing a new detection architecture, this work releases a densely annotated microscopy dataset, a scalable annotation workflow, and a unified benchmark of modern detectors, providing practical guidance for scalable microscopy pipelines and downstream tracking and division analysis.

ArrayVol. 30
University of Debrecen (HU)
Debreceni Egyetem
Openalex Percentile: Top 5%
Cell Image Analysis Techniques
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