Datasets:
Update README.md
#1
by AhmadMM2024 - opened
README.md
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dtype: int32
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splits:
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- name: train
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num_bytes: 303078398
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num_examples: 17092
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download_size: 281772168
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dataset_size: 303078398
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configs:
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- config_name: default
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data_files:
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- split: train
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path: data/train-*
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---
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dtype: int32
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splits:
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- name: train
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num_examples: 17092
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configs:
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- config_name: default
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data_files:
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- split: train
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path: data/train-*
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license: cc-by-4.0
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task_categories:
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- image-classification
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language:
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- en
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tags:
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- microscopy
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- blood
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- hematology
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- blood-cells
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- white-blood-cells
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- medical
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- classification
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pretty_name: PBC (Peripheral Blood Cells)
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size_categories:
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- 10K<n<100K
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---
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# PBC (Peripheral Blood Cells) — Microscopic Images of Normal Peripheral Blood Cells
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This dataset is derived from the **PBC dataset** (Acevedo et al., 2020), a collection of microscopic images of individual normal peripheral blood cells, originally hosted on **Mendeley Data**. The original images were acquired with the CellaVision DM96 analyzer in the core laboratory of the Hospital Clinic of Barcelona and labelled by expert clinical pathologists into eight cell groups.
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Here, we kept the original JPG images unchanged and added the cell type, the cell subtype from the image filename, and an integer label.
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The dataset is designed for blood-cell classification.
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## 📦 Dataset Structure
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The dataset has a single `train` split, with each row corresponding to a single blood-cell image:
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| Field | Description |
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|---|---|
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| `image_id` | Original image filename without extension (e.g., `BA_100102`) |
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| `image` | RGB microscopy image of a single cell (360 × 363 pixels, JPG) |
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| `cell_type` | Cell group: `basophil`, `eosinophil`, `erythroblast`, `ig`, `lymphocyte`, `monocyte`, `neutrophil`, `platelet` |
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| `cell_subtype` | Filename prefix of the original image (e.g., `SNE`, `BNE`, `MY`), which encodes finer subtypes for some groups |
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| `label` | Integer cell group: `0`–`7` (see Feature Descriptions) |
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**Class Distribution:**
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- Basophil: 1,218 images
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- Eosinophil: 3,117 images
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- Erythroblast: 1,551 images
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- Immature granulocyte (IG): 2,895 images
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- Lymphocyte: 1,214 images
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- Monocyte: 1,420 images
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- Neutrophil: 3,329 images
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- Platelet: 2,348 images
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- Total: 17,092 images
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## ⚙️ Preprocessing
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- `PBC_dataset_normal_DIB.zip` was downloaded from Mendeley Data (`snkd93bnjr`, version 1)
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- Images were kept as the original JPG files (no re-encoding, resizing or color normalization)
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- Cell type was taken from each image's parent folder name
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- Cell subtype was taken from the image filename prefix (the part before the last `_`)
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- All images were preserved
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## 🚀 Usage
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```python
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from datasets import load_dataset
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import matplotlib.pyplot as plt
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ds = load_dataset("chehablab/PBC", split="train")
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# One example image per cell group
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classes = ["basophil", "eosinophil", "erythroblast", "ig",
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"lymphocyte", "monocyte", "neutrophil", "platelet"]
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labels = ds["label"]
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fig, axes = plt.subplots(1, len(classes), figsize=(16, 2.6))
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for ax, label in zip(axes, range(len(classes))):
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sample = ds[labels.index(label)]
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ax.imshow(sample["image"])
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ax.set_title(f"{classes[label]}\n{sample['cell_subtype']}")
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ax.axis("off")
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plt.tight_layout()
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plt.show()
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# Filter by cell group
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neutrophils = ds.filter(lambda x: x["cell_type"] == "neutrophil")
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print(f"Neutrophils: {len(neutrophils)}")
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# No official split: make a stratified train/test split
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split = ds.class_encode_column("label").train_test_split(test_size=0.2, stratify_by_column="label", seed=0)
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```
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---
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## 🏷️ Feature Descriptions
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### Cell Groups
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Eight groups of normal peripheral blood cells:
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- **Basophil** (`label=0`): 1,218 images — Granulocyte with large dark-purple granules
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- **Eosinophil** (`label=1`): 3,117 images — Granulocyte with orange-red granules
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- **Erythroblast** (`label=2`): 1,551 images — Nucleated red blood cell precursor
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- **Immature granulocyte, IG** (`label=3`): 2,895 images — Promyelocytes, myelocytes and metamyelocytes
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- **Lymphocyte** (`label=4`): 1,214 images — Mononuclear cell with a round nucleus and scant cytoplasm
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- **Monocyte** (`label=5`): 1,420 images — Large mononuclear cell with a folded or kidney-shaped nucleus
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- **Neutrophil** (`label=6`): 3,329 images — Segmented and band neutrophils
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- **Platelet** (`label=7`): 2,348 images — Platelets (thrombocytes)
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### Image Specifications
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- **Modality**: Brightfield microscopy of peripheral blood smears
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- **Stain**: May Grünwald-Giemsa
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- **Acquisition**: CellaVision DM96 automatic analyzer
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- **Image size**: 360 × 363 pixels, RGB, JPG
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- **Content**: One centered cell per image
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### Acquisition Protocol
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All images were acquired at:
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- **Core Laboratory, Hospital Clinic of Barcelona**, Spain
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- **Subjects**: Individuals without infection, hematologic or oncologic disease, and free of any pharmacological treatment at the time of blood collection
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- **Time period**: 2015 – 2019
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---
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## 🧪 Use Cases
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- Multi-class classification of normal peripheral blood cells
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- White-blood-cell differential counting
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- Fine-grained classification of granulocyte maturation stages (via `cell_subtype`)
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- Representation learning and feature extraction for hematology microscopy
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- Self-supervised pretraining on blood-cell images
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- Reference set of normal cells for abnormal-cell or leukemia detection studies
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## ⚠️ Important Notes
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- **No official split**: The dataset has a single `train` split. Make your own stratified train/validation/test split (see Usage).
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- **No patient IDs**: The original release does not say which images come from the same patient, so a random split can place cells from one smear in both training and evaluation.
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- **Class imbalance**: Neutrophils (3,329) and eosinophils (3,117) are about 2.7× more frequent than lymphocytes (1,214) and basophils (1,218). Use weighted sampling or class balancing as needed.
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- **`cell_subtype`**: This field is read from the original filename prefix and is not an official label; check its values (`ds.to_pandas().groupby(["cell_type", "cell_subtype"]).size()`) before using it.
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- **Normal cells only**: All images come from healthy individuals; the dataset contains no pathological (e.g., leukemic) cells.
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## 📚 Citation
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This dataset is derived from data originally published on **Mendeley Data** under a **CC BY 4.0** license. If you use this dataset, please acknowledge [Chehab Lab](https://chehablab.com) and cite the original PBC dataset:
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```bibtex
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@misc{Acevedo2020PBCData,
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author = {Acevedo, Andrea and Merino, Anna and Alf{\'e}rez, Santiago and Molina, {\'A}ngel and Bold{\'u}, Laura and Rodellar, Jos{\'e}},
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title = {A dataset for microscopic peripheral blood cell images for development of automatic recognition systems [dataset]},
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year = {2020},
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publisher = {Mendeley Data},
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version = {1},
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doi = {10.17632/snkd93bnjr.1}
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}
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```
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Additionally, cite the research paper that introduced this dataset:
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```bibtex
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@article{Acevedo2020PBC,
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author = {Acevedo, Andrea and Merino, Anna and Alf{\'e}rez, Santiago and Molina, {\'A}ngel and Bold{\'u}, Laura and Rodellar, Jos{\'e}},
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title = {A dataset of microscopic peripheral blood cell images for development of automatic recognition systems},
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journal = {Data in Brief},
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volume = {30},
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pages = {105474},
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year = {2020},
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doi = {10.1016/j.dib.2020.105474}
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}
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```
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## ✉️ Original Authors
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**Andrea Acevedo, Anna Merino, Santiago Alférez, Ángel Molina, Laura Boldú, José Rodellar**
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Core Laboratory, Biochemistry and Molecular Genetics Department, Hospital Clinic of Barcelona, and Department of Mathematics, Universitat Politècnica de Catalunya (UPC), Barcelona, Spain
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**Mendeley Data**: https://data.mendeley.com/datasets/snkd93bnjr/1 (original files)
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## 📜 License
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This dataset is released under the **Creative Commons Attribution 4.0 International (CC BY 4.0)** license, consistent with the original PBC dataset.
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You may copy, modify, distribute, and use the data **for any purpose (commercial or non-commercial)**, **provided that appropriate credit is given** to Acevedo et al., Mendeley Data, and the original paper.
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[](https://creativecommons.org/licenses/by/4.0/)
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**Chehab Lab @ 2026**
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