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We present a new annotated microscopic cellular image dataset to improve the effectiveness of machine learning methods for cellular image analysis. Cell counting is an important step in cell analysis. Typically, domain experts manually count cells in a microscopic image. Automated cell counting can potentially eliminate this tedious, time-consuming process. However, a good, labeled dataset is required for training an accurate machine learning model. Our dataset includes microscopic images of cells, and for each image, the cell count and the location of individual cells. The data were collected as part of an ongoing study investigating the potential of electrical stimulation to modulate stem cell differentiation and possible applications for neural repair. Compared to existing publicly available datasets, our dataset has more images of cells stained with more variety of antibodies (protein components of immune responses against invaders) typically used for cell analysis. The experimental results on this dataset indicate that none of the five existing models under this study are able to achieve sufficiently accurate count to replace the manual methods. The dataset is available at https://figshare.com/articles/dataset/Dataset/21970604.
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CellFMCount: A Fluorescence Microscopy Dataset, Benchmark, and Methods for Cell Counting
Abstract—Accurate cell counting is essential in various biomedical research and clinical applications, including cancer diagnosis, stem cell research, and immunology. Manual counting is labor-intensive and error-prone, motivating automation through deep learning techniques. However, training reliable deep learning models requires large amounts of high-quality annotated data, which is difficult and time-consuming to produce manually. Consequently, existing cell-counting datasets are often limited, frequently containing fewer than 500 images. In this work, we introduce a large-scale annotated dataset comprising 3,023 images from immunocytochemistry experiments related to cellular differentiation, containing over 430,000 manually annotated cell locations. The dataset presents significant challenges: high cell density, overlapping and morphologically diverse cells, a long-tailed distribution of cell count per image, and variation in staining protocols. We benchmark three categories of existing methods: regression-based, crowd-counting, and cell-counting techniques on a test set with cell counts ranging from 10 to 2,126 cells per image. We also evaluate how the Segment Anything Model (SAM) can be adapted for microscopy cell counting using only dot-annotated datasets. As a case study, we implement a density-map-based adaptation of SAM (SAM-Counter) and report a mean absolute error (MAE) of 22.12, which outperforms existing approaches (second-best MAE of 27.46). Our results underscore the value of the dataset and the benchmarking framework for driving progress in automated cell counting and provide a robust foundation for future research and development.
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- Award ID(s):
- 2152117
- PAR ID:
- 10678709
- Publisher / Repository:
- IEEE
- Date Published:
- ISBN:
- 979-8-3315-9599-9
- Page Range / eLocation ID:
- 613 to 622
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Cell counting in immunocytochemistry is vital for biomedical research, supporting the diagnosis and treatment of diseases such as neurological disorders, autoimmune conditions, and cancer. However, traditional counting methods are manual, time-consuming, and error-prone, while deep learning solutions require costly labeled datasets, limiting scalability. We introduce the Immunocytochemistry Dataset Cell Counting with Segment Anything Model (IDCC-SAM), a novel application of the Segment Anything Model (SAM), designed to adapt the model for zero-shot-based cell counting in fluorescent microscopic immunocytochemistry datasets. IDCC-SAM leverages Meta AI’s SAM, pre-trained on 11 million images, to eliminate the need for annotations, enhancing scalability and efficiency. Evaluated on three public datasets (IDCIA, ADC, and VGG), IDCC-SAM achieved the lowest Mean Absolute Error (26, 28, 52) on VGG and ADC and the highest Acceptable Absolute Error (28%, 26%, 33%) across all datasets, outperforming state-of-the-art supervised models like U-Net and Mask R-CNN, as well as zero-shot benchmarks like NP-SAM and SAM4Organoid. These results demonstrate IDCC-SAM’s potential to improve cell-counting accuracy while reducing reliance on specialized models and manual annotations.more » « less
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- Free Publicly Accessible Full Text
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Accepted Manuscript
- Conference Paper:
- https://doi.org/10.1109/ICDM65498.2025.00069
