Attribution-NonCommercial 4.0 (CC BY-NC 4.0)https://creativecommons.org/licenses/by-nc/4.0/
License information was derived automatically
If you use this dataset in your research, please credit the authors. Publication Citation: Azamossadat Hosseini, Mohammad Amir (Robin) Eshraghi, Tania Taami, Hamidreza Sadeghsalehi, Zahra Hoseinzadeh, Mustafa Ghaderzadeh, Mohammad Rafiee, A mobile application based on efficient lightweight CNN model for classification of B-ALL cancer from non-cancerous cells: A design and implementation study, Informatics in Medicine Unlocked, Volume 39, 2023, 101244, ISSN 2352-9148, Paper: https://doi.org/10.1016/j.imu.2023.101244. Source code: https://github.com/MAmirEshraghi/Lightweight-Deep-CNN-Based-Mobile-App-in-the-Screening-of-ALL
The definitive diagnosis of Acute Lymphoblastic Leukemia (ALL), as a highly prevalent cancer, requires invasive, expensive, and time-consuming diagnostic tests. ALL diagnosis using peripheral blood smear (PBS) images plays a vital role in the initial screening of cancer from non-cancer cases. The examination of these PBS images by laboratory users is riddled with problems such as diagnostic error because the non-specific nature of ALL signs and symptoms often leads to misdiagnosis.
The images of this dataset were prepared in the bone marrow laboratory of Taleqani Hospital (Tehran, Iran). This dataset consisted of 3242 PBS images from 89 patients suspected of ALL, whose blood samples were prepared and stained by skilled laboratory staff. This dataset is divided into two classes benign and malignant. The former comprises hematogenous, and the latter is the ALL group with three subtypes of malignant lymphoblasts: Early Pre-B, Pre-B, and Pro-B ALL. All the images were taken by using a Zeiss camera in a microscope with a 100x magnification and saved as JPG files. A specialist using the flow cytometry tool made the definitive determination of the types and subtypes of these cells.
http://opendatacommons.org/licenses/dbcl/1.0/http://opendatacommons.org/licenses/dbcl/1.0/
This dataset was created by heewonpark
Released under Database: Open Database, Contents: Database Contents
This dataset was created by Ashiq
https://creativecommons.org/publicdomain/zero/1.0/https://creativecommons.org/publicdomain/zero/1.0/
This dataset was created by Hamzairfan503
Released under CC0: Public Domain
This dataset was created by Johar M. Ashfaque
This dataset was created by Hari Schuth
This dataset was created by Johar M. Ashfaque
It contains the following files:
ALL_IDB_1-2 The ALL_IDB1 version 1.0 can be used both for testing segmentation capability of algorithms, as well as the classification systems and image preprocessing methods. This dataset is composed of 108 images collected during September, 2005. It contains about 150 blood images each class 50 images, where the lymphocytes has been labeled by expert oncologists. The images are taken with different magnifications of the microscope ranging from 300 to 500.
MIT Licensehttps://opensource.org/licenses/MIT
License information was derived automatically
This dataset was created by Shahariar 13
Released under MIT
This dataset was created by zahir4
This dataset was created by Wahidul Hasan Abir
Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
License information was derived automatically
The microscopic blood cell dataset for leukemia detection consists of high-resolution images essential for automated diagnostic systems. Each image captures detailed cellular morphology under standardized conditions, focusing on both normal and abnormal blood cells.
Key Components: - Myeloblasts (AML indicators): 12-20 micrometers, round/oval, high nuclear-cytoplasm ratio, visible nucleoli - Lymphoblasts (ALL indicators): 10-14 micrometers, homogeneous chromatin, minimal cytoplasm - Normal cells: Mature lymphocytes, neutrophils, monocytes, eosinophils, basophils
Technical Specifications: Resolution: 1024x1024 pixels minimum Staining: Wright-Giemsa Magnification: 100x oil immersion (1000x total) Color: 24-bit RGB Multiple focal planes per sample
Quality Measures: Expert hematopathologist validation Standardized imaging conditions Multiple samples per cell type Detailed preparation documentation Complete technical metadata
Clinical Applications: Normal vs. abnormal cell differentiation Leukemia subtype identification Disease progression monitoring Early detection screening Treatment response assessment
Image Annotations Include: Nuclear patterns and contours Cytoplasmic features Nucleoli presence Cell measurements Abnormal inclusions/Auer rods
Machine Learning Capabilities: Automated cell classification Quantitative feature analysis Differential counting Morphological abnormality detection The dataset's structured organization and comprehensive documentation support both research initiatives and clinical applications in blood cancer diagnostics. Its standardized format enables reliable machine learning model development for automated leukemia detection systems.
This dataset consists of 5000 images (.jpg) where the distribution is 1000 per class
Malignant lymphoma is a cancer affecting lymph nodes. Three types of malignant lymphoma are represented in the set: - CLL (chronic lymphocytic leukemia); - FL (follicular lymphoma); - MCL (mantle cell lymphoma).
The ability to distinguish classes of lymphoma from biopsies sectioned and stained with Hematoxylin/Eosin (H+E) would allow for more consistent and less demanding diagnosis of this disease. Only the most expert pathologists specializing in these types of lymphomas are able to consistently and accurately classify these three lymphoma types from H+E-stained biopsies. The standard practice is to use class-specific probes in order to distinguish these classes reliably.
This dataset is a collection of samples prepared by different pathologists at different sites. There is a large degree of staining variation that one would normally expect from such samples.
If you find this dataset useful, please credit the authors
Orlov, Nikita & Chen, Wayne & Eckley, David & Macura, Tomasz & Shamir, Lior & Jaffe, Elaine & Goldberg, Ilya. (2010). Automatic Classification of Lymphoma Images With Transform-Based Global Features. IEEE transactions on information technology in biomedicine : a publication of the IEEE Engineering in Medicine and Biology Society. 14. 1003-13. 10.1109/TITB.2010.2050695.
@article{article, author = {Orlov, Nikita and Chen, Wayne and Eckley, David and Macura, Tomasz and Shamir, Lior and Jaffe, Elaine and Goldberg, Ilya}, year = {2010}, month = {07}, pages = {1003-13}, title = {Automatic Classification of Lymphoma Images With Transform-Based Global Features}, volume = {14}, journal = {IEEE transactions on information technology in biomedicine : a publication of the IEEE Engineering in Medicine and Biology Society}, doi = {10.1109/TITB.2010.2050695} }
License was not specified at the source
Photo by Yassine Khalfalli on Unsplash
https://www.googleapis.com/download/storage/v1/b/kaggle-user-content/o/inbox%2F793761%2F895ec7920df6e19fa16b8831b44d8abc%2FCLL.jpg?generation=1587359355893368&alt=media" alt="CLL">
https://www.googleapis.com/download/storage/v1/b/kaggle-user-content/o/inbox%2F793761%2Fe57c6dfe8e5d68750fd6834449292d0c%2FFL.jpg?generation=1587359386411233&alt=media" alt="FL">
https://www.googleapis.com/download/storage/v1/b/kaggle-user-content/o/inbox%2F793761%2Fab2edfb97c04e39d22ca9d1b467a4063%2FMCL.jpg?generation=1587359404910944&alt=media" alt="MCL">
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Attribution-NonCommercial 4.0 (CC BY-NC 4.0)https://creativecommons.org/licenses/by-nc/4.0/
License information was derived automatically
If you use this dataset in your research, please credit the authors. Publication Citation: Azamossadat Hosseini, Mohammad Amir (Robin) Eshraghi, Tania Taami, Hamidreza Sadeghsalehi, Zahra Hoseinzadeh, Mustafa Ghaderzadeh, Mohammad Rafiee, A mobile application based on efficient lightweight CNN model for classification of B-ALL cancer from non-cancerous cells: A design and implementation study, Informatics in Medicine Unlocked, Volume 39, 2023, 101244, ISSN 2352-9148, Paper: https://doi.org/10.1016/j.imu.2023.101244. Source code: https://github.com/MAmirEshraghi/Lightweight-Deep-CNN-Based-Mobile-App-in-the-Screening-of-ALL
The definitive diagnosis of Acute Lymphoblastic Leukemia (ALL), as a highly prevalent cancer, requires invasive, expensive, and time-consuming diagnostic tests. ALL diagnosis using peripheral blood smear (PBS) images plays a vital role in the initial screening of cancer from non-cancer cases. The examination of these PBS images by laboratory users is riddled with problems such as diagnostic error because the non-specific nature of ALL signs and symptoms often leads to misdiagnosis.
The images of this dataset were prepared in the bone marrow laboratory of Taleqani Hospital (Tehran, Iran). This dataset consisted of 3242 PBS images from 89 patients suspected of ALL, whose blood samples were prepared and stained by skilled laboratory staff. This dataset is divided into two classes benign and malignant. The former comprises hematogenous, and the latter is the ALL group with three subtypes of malignant lymphoblasts: Early Pre-B, Pre-B, and Pro-B ALL. All the images were taken by using a Zeiss camera in a microscope with a 100x magnification and saved as JPG files. A specialist using the flow cytometry tool made the definitive determination of the types and subtypes of these cells.