A survey on automated detection and classification of acute leukemia and WBCs in microscopic blood cells

Leukemia (blood cancer) is an unusual spread of White Blood Cells or Leukocytes (WBCs) in the bone marrow and blood. Pathologists can diagnose leukemia by looking at a person's blood sample under a microscope. They identify and categorize leukemia by counting various blood cells and morphological features. This technique is time-consuming for the prediction of leukemia. The pathologist's professional skills and experiences may be affecting this procedure, too. In computer vision, traditional machine learning and deep learning techniques are practical roadmaps that increase the accuracy and speed in diagnosing and classifying medical images such as microscopic blood cells. This paper provides a comprehensive analysis of the detection and classification of acute leukemia and WBCs in the microscopic blood cells. First, we have divided the previous works into six categories based on the output of the models. Then, we describe various steps of detection and classification of acute leukemia and WBCs, including Data Augmentation, Preprocessing, Segmentation, Feature Extraction, Feature Selection (Reduction), Classification, and focus on classification step in the methods. Finally, we divide automated detection and classification of acute leukemia and WBCs into three categories, including traditional, Deep Neural Network (DNN), and mixture (traditional and DNN) methods based on the type of classifier in the classification step and analyze them. The results of this study show that in the diagnosis and classification of acute leukemia and WBCs, the Support Vector Machine (SVM) classifier in traditional machine learning models and Convolutional Neural Network (CNN) classifier in deep learning models have widely employed. The performance metrics of the models that use these classifiers compared to the others model are higher

Peripheral Blood Smear Analyses Using Deep Learning

Peripheral Blood Smear (PBS) analysis is a vital routine test carried out by hematologists to assess some aspects of humans’ health status. PBS analysis is prone to human errors and utilizing computer-based analysis can greatly enhance this process in terms of accuracy and cost. Recent approaches in learning algorithms, such as deep learning, are data hungry, but due to the scarcity of labeled medical images, researchers had to find viable alternative solutions to increase the size of available datasets. Synthetic datasets provide a promising solution to data scarcity, however, the complexity of blood smears’ natural structure adds an extra layer of challenge to its synthesizing process. In this thesis, we propose a method- ology that utilizes Locality Sensitive Hashing (LSH) to create a novel balanced dataset of synthetic blood smears. This dataset, which was automatically annotated during the gener- ation phase, covers 17 essential categories of blood cells. The dataset also got the approval of 5 experienced hematologists to meet the general standards of making thin blood smears. Moreover, a platelet classifier and a WBC classifier were trained on the synthetic dataset. For classifying platelets, a hybrid approach of deep learning and image processing tech- niques is proposed. This approach improved the platelet classification accuracy and macro- average precision from 82.6% to 98.6% and 76.6% to 97.6% respectively. Moreover, for white blood cell classification, a novel scheme for training deep networks is proposed, namely, Enhanced Incremental Training, that automatically recognises and handles classes that confuse and negatively affect neural network predictions. To handle the confusable classes, we also propose a procedure called "training revert". Application of the proposed method has improved the classification accuracy and macro-average precision from 61.5% to 95% and 76.6% to 94.27% respectively. In addition, the feasibility of using animal reticulocyte cells as a viable solution to com- pensate for the deficiency of human data is investigated. The integration of animal cells is implemented by employing multiple deep classifiers that utilize transfer learning in differ- ent experimental setups in a procedure that mimics the protocol followed in experimental medical labs. Moreover, three measures are defined, namely, the pretraining boost, the dataset similarity boost, and the dataset size boost measures to compare the effectiveness of the utilized experimental setups. All the experiments of this work were conducted on a novel public human reticulocyte dataset and the best performing model achieved 98.9%, 98.9%, 98.6% average accuracy, average macro precision, and average macro F-score re- spectively. Finally, this work provides a comprehensive framework for analysing two main blood smears that are still being conducted manually in labs. To automate the analysis process, a novel method for constructing synthetic whole-slide blood smear datasets is proposed. Moreover, to conduct the blood cell classification, which includes eighteen blood cell types and abnormalities, two novel techniques are proposed, namely: enhanced incremental train- ing and animal to human cells transfer learning. The outcomes of this work were published in six reputable international conferences and journals such as the computers in biology and medicine and IEEE access journals