Classification Of White Blood Cells Research Articles

Classification of white blood cells (leucocytes) from blood smear imagery using machine and deep learning models: A global scoping review.

Machine learning (ML) and deep learning (DL) models are being increasingly employed for medical imagery analyses, with both approaches used to enhance the accuracy of classification/prediction in the diagnoses of various cancers, tumors and bloodborne diseases. To date however, no review of these techniques and their application(s) within the domain of white blood cell (WBC) classification in blood smear images has been undertaken, representing a notable knowledge gap with respect to model selection and comparison. Accordingly, the current study sought to comprehensively identify, explore and contrast ML and DL methods for classifying WBCs. Following development and implementation of a formalized review protocol, a cohort of 136 primary studies published between January 2006 and May 2023 were identified from the global literature, with the most widely used techniques and best-performing WBC classification methods subsequently ascertained. Studies derived from 26 countries, with highest numbers from high-income countries including the United States (n = 32) and The Netherlands (n = 26). While WBC classification was originally rooted in conventional ML, there has been a notable shift toward the use of DL, and particularly convolutional neural networks (CNN), with 54.4% of identified studies (n = 74) including the use of CNNs, and particularly in concurrence with larger datasets and bespoke features e.g., parallel data pre-processing, feature selection, and extraction. While some conventional ML models achieved up to 99% accuracy, accuracy was shown to decrease in concurrence with decreasing dataset size. Deep learning models exhibited improved performance for more extensive datasets and exhibited higher levels of accuracy in concurrence with increasingly large datasets. Availability of appropriate datasets remains a primary challenge, potentially resolvable using data augmentation techniques. Moreover, medical training of computer science researchers is recommended to improve current understanding of leucocyte structure and subsequent selection of appropriate classification models. Likewise, it is critical that future health professionals be made aware of the power, efficacy, precision and applicability of computer science, soft computing and artificial intelligence contributions to medicine, and particularly in areas like medical imaging.

Label-free white blood cells classification using a deep feature fusion neural network

White blood cell (WBC) classification is a valuable diagnostic approach for identifying diseases. However, conventional methods for WBC detection, such as flow cytometers, have limitations in terms of their high cost, large system size, and laborious staining procedures. As a result, deep learning-based label-free WBC image analysis methods are gaining popularity. Nevertheless, most existing deep learning WBC classification techniques fail to effectively utilize the subtle differences in the internal structures of WBCs observed under a microscope. To address this issue, we propose a neural network with feature fusion in this study, which enables the detection of label-free WBCs. Unlike conventional convolutional neural networks (CNNs), our approach combines low-level features extracted by shallow layers with high-level features extracted by deep layers, generating fused features for accurate bright-field WBC identification. Our method achieves an accuracy of 80.3 % on the testing set, demonstrating a potential solution for deep-learning-based biomedical diagnoses. Considering the proposed method simplifies the cell detection process and eliminates the need for complex operations like fluorescent staining, we anticipate that this automatic and label-free WBC classification network could facilitate more precise and effective analysis, and it could contribute to the future adoption of miniatured flow cytometers for point-of-care (POC) diagnostics applications.

SURVEY ON WBC CLASSIFICATION AND DETECTION USING YOLO

Our heart pumps red blood constantly, carrying waste products, hormones, nutrition, oxygen, and other essential health markers. Blood cells in this fluid are made up of many components, including platelets, RBCs, and WBCs. Neutrophils, Lymphocytes, Monocytes, Eosinophils, and Basophils are further subdivided into WBCs. To precisely identify and treat numerous kinds of blood-related illnesses, the detection and analysis of these blood cells is necessary for advanced diagnostics in medicine. Convolutional neural networks (CNNs), for example, are highly relied upon in modern medical diagnostics for the examination of blood cells. The precision and potency of blood cell identification procedures have been greatly improved by CNNs and Additional approaches to deep learning like RNNs and YOLO. The persistence of this research is to list challenges in White Blood cell detection and classification problem. Deep learning-based blood cell identification and classification approaches based on Single Stage approaches. Single Stage Approach involve You only look Once (YOLO). It explores the various architectures for feature selection and classification starting from YoloV1 toV5 and it’s various modifications. In this paper would be looking at things like network parameters, training procedure, and transfer learning application for each variation. It also assesses model complexity, accuracy, performance, generalization, computational efficiency, and transfer learning capabilities, in addition to variables like data amount and source.

A hybrid approach based on multipath Swin transformer and ConvMixer for white blood cells classification

White blood cells (WBC) play an effective role in the body’s defense against parasites, viruses, and bacteria in the human body. Also, WBCs are categorized based on their morphological structures into various subgroups. The number of these WBC types in the blood of non-diseased and diseased people is different. Thus, the study of WBC classification is quite significant for medical diagnosis. Due to the widespread use of deep learning in medical image analysis in recent years, it has also been used in WBC classification. Moreover, the ConvMixer and Swin transformer models, recently introduced, have garnered significant success by attaining efficient long contextual characteristics. Based on this, a new multipath hybrid network is proposed for WBC classification by using ConvMixer and Swin transformer. This proposed model is called Swin Transformer and ConvMixer based Multipath mixer (SC-MP-Mixer). In the SC-MP-Mixer model, firstly, features with strong spatial details are extracted with the ConvMixer. Then Swin transformer effectively handle these features with self-attention mechanism. In addition, the ConvMixer and Swin transformer blocks consist of a multipath structure to obtain better patch representations in the SC-MP-Mixer. To test the performance of the SC-MP-Mixer, experiments were performed on three WBC datasets with 4 (BCCD), 8 (PBC) and 5 (Raabin) classes. The experimental studies resulted in an accuracy of 99.65% for PBC, 98.68% for Raabin, and 95.66% for BCCD. When compared with the studies in the literature and the state-of-the-art models, it was seen that the SC-MP-Mixer had more effective classification results.

Deep transfer learning technique to detect white blood cell classification in regular clinical practice using histopathological images

Deep transfer learning technique to detect white blood cell classification in regular clinical practice using histopathological images

AI-Based Portable White Blood Cells Classification and Counting System in POCT

AI-Based Portable White Blood Cells Classification and Counting System in POCT

White blood cells classification using multi-fold pre-processing and optimized CNN model

White blood cells (WBCs) play a vital role in immune responses against infections and foreign agents. Different WBC types exist, and anomalies within them can indicate diseases like leukemia. Previous research suffers from limited accuracy and inflated performance due to the usage of less important features. Moreover, these studies often focus on fewer WBC types, exaggerating accuracy. This study addresses the crucial task of classifying WBC types using microscopic images. This study introduces a novel approach using extensive pre-processing with data augmentation techniques to produce a more significant feature set to achieve more promising results. The study conducts experiments employing both conventional deep learning and transfer learning models, comparing performance with state-of-the-art machine and deep learning models. Results reveal that a pre-processed feature set and convolutional neural network classifier achieves a significantly better accuracy of 0.99. The proposed method demonstrates superior accuracy and computational efficiency compared to existing state-of-the-art works.

Automatic Classification of White Blood Cells Using a Semi-Supervised Convolutional Neural Network

Automatic Classification of White Blood Cells Using a Semi-Supervised Convolutional Neural Network

Improved Generalization of White Blood Cell Classification by Learnable Illumination Intensity Invariant Layer

Improved Generalization of White Blood Cell Classification by Learnable Illumination Intensity Invariant Layer

WBC YOLO-ViT: 2 Way - 2 stage white blood cell detection and classification with a combination of YOLOv5 and vision transformer

Accurate detection and classification of white blood cells, otherwise known as leukocytes, play a critical role in diagnosing and monitoring various illnesses. However, conventional methods, such as manual classification by trained professionals, must be revised in terms of accuracy, efficiency, and potential bias. Moreover, applying deep learning techniques to detect and classify white blood cells using microscopic images is challenging owing to limited data, resolution noise, irregular shapes, and varying colors from different sources. This study presents a novel approach integrating object detection and classification for numerous type-white blood cell. We designed a 2-way approach to use two types of images: WBC and nucleus. YOLO (fast object detection) and ViT (powerful image representation capabilities) are effectively integrated into 16 classes. The proposed model demonstrates an exceptional 96.449% accuracy rate in classification.

Retracted: Deep Learning Model for the Automatic Classification of White Blood Cells.

[This retracts the article DOI: 10.1155/2022/7384131.].

A Deep Learning Framework for Classification of Immature White Blood Cells in Acute Myeloid Leukemia Using Convolutional Autoencoder and Transfer-Learning Ensemble

Acute myeloid leukemia (AML) is a type of acute leukemia that affects myeloid cells. It is characterized by uncontrolled proliferation of immature WBCs causing an accumulation of immature WBCs in the bone marrow and peripheral circulation. AML is an aggressive cancer that can be life-threatening if not treated promptly, therefore, early detection is crucial. Identification of immature WBCs and their subtypes is the first step towards AML diagnosis. Microscopic blood smear image analysis is commonly used to diagnose AML as it is less expensive non-invasive diagnostic tool compared to bone marrow biopsy and immunophenotype. Nonetheless, classifying immature WBCs presents challenges due to their high similarity and minimal interclass variation, especially for intermediate stages of myelopoiesis which make is susceptible to misclassification. The current diagnostic methods of AML are based on manual identification of immature WBCs using peripheral blood smear. These methos are time-consuming, prone to errors, and subject to inter-observer variation. Therefore, this study aims to develop a computer-aided diagnostic framework to accurately identify immature WBCs and classify them into various subtypes. The proposed framework consists of two main components: a binary classification system to classify cells into mature versus immature cells and a multiclassification system to further classify immature cells into four subtypes including myeloblast, monoblast, and promyelocytes. The proposed framework was designed to undergo four distinct phases: the first phase involves preprocessing, which includes data augmentation techniques aimed at addressing the imbalance distribution of WBCs. Augmentation encompasses geometric transformation and generation of synthetic images using convolutional Autoencoder (CAE). Feature extraction phase involves using image embedding and transfer-learning. Image embedding representation was obtained using CAE and then utilized by two pre-trained models: VGG19 and Resnet50. Classification phase was carried out using weighted ensemble of the VGG19 and Resnet50 with the optimal weights determined through Grid search. The validation phase evaluated the model performance using overall accuracy, precision, and sensitivity. The area under the ROC curve (AUC) was used to assess model discrimination ability. The proposed framework demonstrated excellent results, achieving an average accuracy of 99.5%, a sensitivity of 97.97%, and a precision of 94.12%. The model exhibited an excellent discriminatory capability, with an AUC of 99.9%. Furthermore, the proposed framework outperformed previous methods, showcasing improved performance. Key word: Acute myeloid leukemia, peripheral blood smear, immature white blood cells, deep learning, feature extraction, computer-aided diagnosis.

White Blood Cell Classification: Convolutional Neural Network (CNN) and Vision Transformer (ViT) under Medical Microscope

Deep learning (DL) has made significant advances in computer vision with the advent of vision transformers (ViTs). Unlike convolutional neural networks (CNNs), ViTs use self-attention to extract both local and global features from image data, and then apply residual connections to feed these features directly into a fully networked multilayer perceptron head. In hospitals, hematologists prepare peripheral blood smears (PBSs) and read them under a medical microscope to detect abnormalities in blood counts such as leukemia. However, this task is time-consuming and prone to human error. This study investigated the transfer learning process of the Google ViT and ImageNet CNNs to automate the reading of PBSs. The study used two online PBS datasets, PBC and BCCD, and transferred them into balanced datasets to investigate the influence of data amount and noise immunity on both neural networks. The PBC results showed that the Google ViT is an excellent DL neural solution for data scarcity. The BCCD results showed that the Google ViT is superior to ImageNet CNNs in dealing with unclean, noisy image data because it is able to extract both global and local features and use residual connections, despite the additional time and computational overhead.

A-144 Three-wavelength Polarization Imaging Method for the Analysis of Individual Human Blood Cells With Dye-Enhanced Dispersion of Dilution Buffer

Abstract Background Performing basic hematology analysis in a near-patient setting enables more rapid clinical decision making in the process of diagnosis. Traditional blood analyzers in central labs use a complex combination of sensing principles and chemical modification of the sample to derive the necessary parameters for a complete blood count (CBC). To reduce cost and maintenance, varying approaches have been employed to determine a CBC with a single-step measurement technique. One common option is the use of optical microscopy to deliver highly reliable results, examples are fluorescence microscopy, digital holographic microscopy, or spatial light interference microscopy. However, most of these technologies lack a proper determination of cellular-level RBC parameters. Therefore, a non-interferometric, quantitative-phase measurement technique was developed to derive relevant CBC parameters from a single measurement, comparable to a standard lab analyzer. Methods The optical setup employed by this method enables the parallel acquisition of brightfield and differential interference contrast (DIC) images by polarization-sensitive cameras. By using three cameras with individual optical filters, quantitative phase and absorption information can be calculated, which enables the determination of mean cellular volume (MCV), mean cellular hemoglobin (MCH), and mean cellular hemoglobin concentration (MCHC) for red blood cells (RBCs). The whole-blood sample is diluted in a buffer containing a non-cell-penetrating dye to enhance optical refraction contrast and therefore precision in the dependent calculated quantities. The sample is then introduced to a glass flow cell, and the cells are allowed to sediment to the bottom for imaging. Machine learning is applied to the derived images to classify unstained native white blood cells (WBCs) to yield a 5-part differential, which distinguishes between neutrophil, monocyte, lymphocyte, eosinophil and basophil. The algorithm is trained by imaging FACS-validated, purified WBC subgroups. All blood samples are measured on an ADVIA® 2120 Hematology System for control. Results A one-step, optical CBC hematology system based on quantitative phase and absorption image analysis was developed. The correlations for MCV and MCHC compared to a standard lab CBC analyzer were 0.77 and 0.84. The accuracy for the 5-part differential WBC classification was approximately 0.8. To enable a visual inspection of the classification results, a pseudo-colored image of each cell was generated and uploaded in a review tool. Conclusion With a more-refined, less-expensive optical setup, a high-quality CBC analyzer suitable for use at the point of care can be derived with the presented method. A possible simplification could be the use of low-cost but high-resolution Fourier ptychography microscopy (FPM) technology. Imaging of blood samples on a single-cell level offers the potential for the analysis of even more morphological parameters, for example, disease-related changes in the cell membrane. Also, the adhesion behavior of the WBCs in the glass flow cell could indicate cell activation status and therefore give information about infection processes. *Trademark disclaimer: “ADVIA, and all associated marks are trademarks of Siemens Healthcare Diagnostics, Inc. or its affiliates. All other trademarks and brands are the property of their respective owners.”

Red Deer Optimization with Deep Learning based Robust White Blood Cell Detection and Classification Model

The use of deep learning techniques for White Blood Cell (WBC) classification has garnered significant attention on medical image analysis due to its potential to automate and enhance the accuracy of WBC classification, which is critical for disease diagnosis and infection detection. Convolutional neural networks (CNNs) have revolutionized image analysis tasks, including WBC classification effectively capturing intricate spatial patterns and distinguishing between different cell types. A key advantage of deep learning-based WBC classification is its capability to handle large datasets, enabling models to learn the diverse variations and characteristics of different cell types. This facilitates robust generalization and accurate classification of previously unseen samples. In this paper, a novel approach called Red Deer Optimization with Deep Learning for Robust White Blood Cell Detection and Classification was presented. The proposed model incorporates various components to improve performance and robustness. Image pre-processing involves the utilization of median filtering, while U-Net++ is employed for segmentation, facilitating accurate delineation of WBCs. Feature extraction is performed using the Xception model, which effectively captures informative representations of the WBCs. For classification, BiGRU model is employed, leveraging its ability to model temporal dependencies in the WBC sequences. To optimize the performance of the BiGRU model, the RDO is utilized for parameter tuning, resulting in enhanced accuracy and faster convergence of the deep learning models. The integration of RDO contributes to more reliable detection and classification of WBCs, further improving the overall performance and robustness of the approach. Experimental results demonstrate the superiority of our Red Deer Optimization with deep learning-based approach over traditional methods and standalone deep learning models in achieving robust WBC detection and classification. This research highlights the possibility of combining deep learning techniques with optimization algorithms for improving WBC analysis, offering valuable insights for medical professionals and medical image analysis.

Using deep DenseNet with cyclical learning rate to classify leukocytes for leukemia identification.

The examination, counting, and classification of white blood cells (WBCs), also known as leukocytes, are essential processes in the diagnosis of many disorders, including leukemia, a kind of blood cancer characterized by the uncontrolled proliferation of carcinogenic leukocytes in the marrow of the bone. Blood smears can be chemically or microscopically studied to better understand hematological diseases and blood disorders. Detecting, identifying, and categorizing the many blood cell types are essential for disease diagnosis and therapy planning. A theoretical and practical issue. However, methods based on deep learning (DL) have greatly helped blood cell classification. Images of blood cells in a microscopic smear were collected from GitHub, a public source that uses the MIT license. An end-to-end computer-aided diagnosis (CAD) system for leukocytes has been created and implemented as part of this study. The introduced system comprises image preprocessing and enhancement, image segmentation, feature extraction and selection, and WBC classification. By combining the DenseNet-161 and the cyclical learning rate (CLR), we contribute an approach that speeds up hyperparameter optimization. We also offer the one-cycle technique to rapidly optimize all hyperparameters of DL models to boost training performance. The dataset has been split into two sets: approximately 80% of the data (9,966 images) for the training set and 20% (2,487 images) for the validation set. The validation set has 623, 620, 620, and 624 eosinophil, lymphocyte, monocyte, and neutrophil images, whereas the training set has 2,497, 2,483, 2,487, and 2,499, respectively. The suggested method has 100% accuracy on the training set of images and 99.8% accuracy on the testing set. Using a combination of the recently developed pretrained convolutional neural network (CNN), DenseNet, and the one fit cycle policy, this study describes a technique of training for the classification of WBCs for leukemia detection. The proposed method is more accurate compared to the state of the art.

UR-Net: An Integrated ResUNet and Attention Based Image Enhancement and Classification Network for Stain-Free White Blood Cells.

The differential count of white blood cells (WBCs) can effectively provide disease information for patients. Existing stained microscopic WBC classification usually requires complex sample-preparation steps, and is easily affected by external conditions such as illumination. In contrast, the inconspicuous nuclei of stain-free WBCs also bring great challenges to WBC classification. As such, image enhancement, as one of the preprocessing methods of image classification, is essential in improving the image qualities of stain-free WBCs. However, traditional or existing convolutional neural network (CNN)-based image enhancement techniques are typically designed as standalone modules aimed at improving the perceptual quality of humans, without considering their impact on advanced computer vision tasks of classification. Therefore, this work proposes a novel model, UR-Net, which consists of an image enhancement network framed by ResUNet with an attention mechanism and a ResNet classification network. The enhancement model is integrated into the classification model for joint training to improve the classification performance for stain-free WBCs. The experimental results demonstrate that compared to the models without image enhancement and previous enhancement and classification models, our proposed model achieved a best classification performance of 83.34% on our stain-free WBC dataset.

Integrating explainability into deep learning-based models for white blood cells classification

White blood cells (WBCs) are crucial constituents of the blood that protect the human body against infections and viruses. The classification of WBCs in a blood smear image is used to diagnose a range of haematological disorders. The manual identification of WBCs can result in potential errors, necessitating the need for automated systems that can assist in classification. Recently, various deep learning models, such as DenseNet121, Xception, MobileNetV2, ResNet50, and VGG16, have been used to classify WBCs. However, the available classification models are black boxes because their decisions are difficult for humans to understand without further exploration. The interpretability and explainability of these models are essential, as their decisions can have severe consequences for patients. In this paper, we integrate an explainable AI (XAI) technique called local interpretable model-agnostic explanations (LIME) with the DenseNet121 classification model for WBC classification. Interpretable results would allow the users to understand and verify the model’s predictions, enhancing their confidence in the automated diagnosis.

An Explainable Vision Transformer Model Based White Blood Cells Classification and Localization.

White blood cells (WBCs) are crucial components of the immune system that play a vital role in defending the body against infections and diseases. The identification of WBCs subtypes is useful in the detection of various diseases, such as infections, leukemia, and other hematological malignancies. The manual screening of blood films is time-consuming and subjective, leading to inconsistencies and errors. Convolutional neural networks (CNN)-based models can automate such classification processes, but are incapable of capturing long-range dependencies and global context. This paper proposes an explainable Vision Transformer (ViT) model for automatic WBCs detection from blood films. The proposed model uses a self-attention mechanism to extract features from input images. Our proposed model was trained and validated on a public dataset of 16,633 samples containing five different types of WBCs. As a result of experiments on the classification of five different types of WBCs, our model achieved an accuracy of 99.40%. Moreover, the model's examination of misclassified test samples revealed a correlation between incorrect predictions and the presence or absence of granules in the cell samples. To validate this observation, we divided the dataset into two classes, Granulocytes and Agranulocytes, and conducted a secondary training process. The resulting ViT model, trained for binary classification, achieved impressive performance metrics during the test phase, including an accuracy of 99.70%, recall of 99.54%, precision of 99.32%, and F-1 score of 99.43%. To ensure the reliability of the ViT model's, we employed the Score-CAM algorithm to visualize the pixel areas on which the model focuses during its predictions. Our proposed method is suitable for clinical use due to its explainable structure as well as its superior performance compared to similar studies in the literature. The classification and localization of WBCs with this model can facilitate the detection and reporting process for the pathologist.

Classification of white blood cells based on modified U‐Net and SVM

SummaryManual investigation of blood cell count is sometimes erroneous due to interoperability error, fatigue error, requiring expert skill and time consuming too. In particular, investigation of white blood cell (WBC) gains importance in identifying diseases like leukemia, leukopenia, etc. WBC does not possess regular structure because they move throughout the blood stream and hence analyzing WBC and its types for structure and shape is quite challenging. To aid in hematology, this work provides classification of WBC classification based on modified U‐Net and support vector machines (SVM). A modified U‐Net architecture is developed to segment WBC followed by feature extraction and classification by radial basis function‐support vector machine (RBF‐SVM). Experiments indicated that the modified U Net segmentation can detect the WBC nucleus with a dice similarity coefficient of 0.972. The proposed U‐Net‐SVM can recognize WBCs in Raabin‐WBC, LISC, and BCCD datasets with an accuracy of 99.45%, 98.62%, and 98.81%, respectively. Further investigation on leukemia dataset, ALL‐IDB2, revealed an accuracy of 99.42% with 100% sensitivity and specificity. The proposed model can be used to investigate WBCs and hence provide a great support to the hematologists in analyzing the blood smear for various disease identifications.