Temporal - spatial recognizer for multi-label data

Pattern recognition is an important artificial intelligence task with practical applications in many fields such as medical and species distribution. Such application involves overlapping data points which are demonstrated in the multi- label dataset. Hence, there is a need for a recognition algorithm that can separate the overlapping data points in order to recognize the correct pattern. Existing recognition methods suffer from sensitivity to noise and overlapping points as they could not recognize a pattern when there is a shift in the position of the data points. Furthermore, the methods do not implicate temporal information in the process of recognition, which leads to low quality of data clustering. In this study, an improved pattern recognition method based on Hierarchical Temporal Memory (HTM) is proposed to solve the overlapping in data points of multi- label dataset. The imHTM (Improved HTM) method includes improvement in two of its components; feature extraction and data clustering. The first improvement is realized as TS-Layer Neocognitron algorithm which solves the shift in position problem in feature extraction phase. On the other hand, the data clustering step, has two improvements, TFCM and cFCM (TFCM with limit- Chebyshev distance metric) that allows the overlapped data points which occur in patterns to be separated correctly into the relevant clusters by temporal clustering. Experiments on five datasets were conducted to compare the proposed method (imHTM) against statistical, template and structural pattern recognition methods. The results showed that the percentage of success in recognition accuracy is 99% as compared with the template matching method (Featured-Based Approach, Area-Based Approach), statistical method (Principal Component Analysis, Linear Discriminant Analysis, Support Vector Machines and Neural Network) and structural method (original HTM). The findings indicate that the improved HTM can give an optimum pattern recognition accuracy, especially the ones in multi- label dataset

Conditional spatial biased intuitionistic clustering technique for brain MRI image segmentation

In clinical research, it is crucial to segment the magnetic resonance (MR) brain image for studying the internal tissues of the brain. To address this challenge in a sustainable manner, a novel approach has been proposed leveraging the power of unsupervised clustering while integrating conditional spatial properties of the image into intuitionistic clustering technique for segmenting MRI images of brain scans. In the proposed technique, an Intuitionistic-based clustering approach incorporates a nuanced understanding of uncertainty inherent in the image data. The measure of uncertainty is achieved through calculation of hesitation degree. The approach introduces a conditional spatial function alongside the intuitionistic membership matrix, enabling the consideration of spatial relationships within the image. Furthermore, by calculating weighted intuitionistic membership matrix, the algorithm gains the ability to adapt its smoothing behavior based on the local context. The main advantages are enhanced robustness with homogenous segments, lower sensitivity to noise, intensity inhomogeneity and accommodation of degree of hesitation or uncertainty that may exist in the real-world datasets. A comparative analysis of synthetic and real datasets of MR brain images proves the efficiency of the suggested approach over different algorithms. The paper investigates how the suggested research methodology performs in medical industry under different circumstances including both qualitative and quantitative parameters such as segmentation accuracy, similarity index, true positive ratio, false positive ratio. The experimental outcomes demonstrate that the suggested algorithm outperforms in retaining image details and achieving segmentation accuracy

FCM Clustering Algorithms for Segmentation of Brain MR Images

The study of brain disorders requires accurate tissue segmentation of magnetic resonance (MR) brain images which is very important for detecting tumors, edema, and necrotic tissues. Segmentation of brain images, especially into three main tissue types: Cerebrospinal Fluid (CSF), Gray Matter (GM), and White Matter (WM), has important role in computer aided neurosurgery and diagnosis. Brain images mostly contain noise, intensity inhomogeneity, and weak boundaries. Therefore, accurate segmentation of brain images is still a challenging area of research. This paper presents a review of fuzzy c-means (FCM) clustering algorithms for the segmentation of brain MR images. The review covers the detailed analysis of FCM based algorithms with intensity inhomogeneity correction and noise robustness. Different methods for the modification of standard fuzzy objective function with updating of membership and cluster centroid are also discussed

Approche robuste pour la segmentation et la classification d’images m´edicales

Image segmentation is a vital process in various fields, including robotics, object recognition, and medical imaging. In medical imaging, accurate segmentation of brain tissues from MRI images is crucial for diagnosing and treating brain disorders such as Alzheimer’s disease, epilepsy, schizophrenia, multiple sclerosis, and cancer. This thesis proposes an automatic fuzzy method for brain MRI segmentation. Firstly, the proposed method aims to improve the efficiency of the Fuzzy C-Means (FCM) algorithm by reducing the need for manual intervention in cluster initialization and determining the number of clusters. For this purpose, we introduce an adaptive splitmerge technique that effectively divides the image into several homogeneous regions using a multi-threshold method based on entropy information. During the merge process, a new distance metric is introduced to combine the regions that are both highly similar within the merged region and effectively separated from others. The cluster centers and numbers obtained from the adaptive split-merge step serve as the initial parameters for the FCM algorithm. The obtained fuzzy partitions are evaluated using a novel proposed validity index. Secondly, we present a novel method to address the challenge of noisy pixels in the FCM algorithm by incorporating spatial information. Specifically, we assign a crucial role to the central pixel in the clustering process, provided it is not corrupted with noise. However, if it is corrupted with noise, its influence is reduced. Furthermore, we propose a novel quantitative metric for replacing the central pixel with one of its neighbors if it can improve the segmentation result in terms of compactness and separation. To evaluate the effectiveness of the proposed method, a thorough comparison with existing clustering techniques is conducted, considering cluster validity functions, segmentation accuracy, and tissue segmentation accuracy. The evaluation comprises comprehensive qualitative and quantitative assessments, providing strong evidence of the superior performance of the proposed approach

Hematological image analysis for acute lymphoblastic leukemia detection and classification

Microscopic analysis of peripheral blood smear is a critical step in detection of leukemia.However, this type of light microscopic assessment is time consuming, inherently subjective, and is governed by hematopathologists clinical acumen and experience. To circumvent such problems, an efficient computer aided methodology for quantitative analysis of peripheral blood samples is required to be developed. In this thesis, efforts are therefore made to devise methodologies for automated detection and subclassification of Acute Lymphoblastic Leukemia (ALL) using image processing and machine learning methods.Choice of appropriate segmentation scheme plays a vital role in the automated disease recognition process. Accordingly to segment the normal mature lymphocyte and malignant lymphoblast images into constituent morphological regions novel schemes have been proposed. In order to make the proposed schemes viable from a practical and real–time stand point, the segmentation problem is addressed in both supervised and unsupervised framework. These proposed methods are based on neural network,feature space clustering, and Markov random field modeling, where the segmentation problem is formulated as pixel classification, pixel clustering, and pixel labeling problem respectively. A comprehensive validation analysis is presented to evaluate the performance of four proposed lymphocyte image segmentation schemes against manual segmentation results provided by a panel of hematopathologists. It is observed that morphological components of normal and malignant lymphocytes differ significantly. To automatically recognize lymphoblasts and detect ALL in peripheral blood samples, an efficient methodology is proposed.Morphological, textural and color features are extracted from the segmented nucleus and cytoplasm regions of the lymphocyte images. An ensemble of classifiers represented as EOC3 comprising of three classifiers shows highest classification accuracy of 94.73% in comparison to individual members. The subclassification of ALL based on French–American–British (FAB) and World Health Organization (WHO) criteria is essential for prognosis and treatment planning. Accordingly two independent methodologies are proposed for automated classification of malignant lymphocyte (lymphoblast) images based on morphology and phenotype. These methods include lymphoblast image segmentation, nucleus and cytoplasm feature extraction, and efficient classification

Methodology for automatic classification of atypical lymphoid cells from peripheral blood cell images

Morphological analysis is the starting point for the diagnostic approach of more than 80% of the hematological diseases. However, the morphological differentiation among different types of abnormal lymphoid cells in peripheral blood is a difficult task, which requires high experience and skill. Objective values do not exist to define cytological variables, which sometimes results in doubts on the correct cell classification in the daily hospital routine. Automated systems exist which are able to get an automatic preclassification of the normal blood cells, but fail in the automatic recognition of the abnormal lymphoid cells. The general objective of this thesis is to develop a complete methodology to automatically recognize images of normal and reactive lymphocytes, and several types of neoplastic lymphoid cells circulating in peripheral blood in some mature B-cell neoplasms using digital image processing methods. This objective follows two directions: (1) with engineering and mathematical background, transversal methodologies and software tools are developed; and (2) with a view towards the clinical laboratory diagnosis, a system prototype is built and validated, whose input is a set of pathological cell images from individual patients, and whose output is the automatic classification in one of the groups of the different pathologies included in the system. This thesis is the evolution of various works, starting with a discrimination between normal lymphocytes and two types of neoplastic lymphoid cells, and ending with the design of a system for the automatic recognition of normal lymphocytes and five types of neoplastic lymphoid cells. All this work involves the development of a robust segmentation methodology using color clustering, which is able to separate three regions of interest: cell, nucleus and peripheral zone around the cell. A complete lymphoid cell description is developed by extracting features related to size, shape, texture and color. To reduce the complexity of the process, a feature selection is performed using information theory. Then, several classifiers are implemented to automatically recognize different types of lymphoid cells. The best classification results are achieved using support vector machines with radial basis function kernel. The methodology developed, which combines medical, engineering and mathematical backgrounds, is the first step to design a practical hematological diagnosis support tool in the near future.Los análisis morfológicos son el punto de partida para la orientación diagnóstica en más del 80% de las enfermedades hematológicas. Sin embargo, la clasificación morfológica entre diferentes tipos de células linfoides anormales en la sangre es una tarea difícil que requiere gran experiencia y habilidad. No existen valores objetivos para definir variables citológicas, lo que en ocasiones genera dudas en la correcta clasificación de las células en la práctica diaria en un laboratorio clínico. Existen sistemas automáticos que realizan una preclasificación automática de las células sanguíneas, pero no son capaces de diferenciar automáticamente las células linfoides anormales. El objetivo general de esta tesis es el desarrollo de una metodología completa para el reconocimiento automático de imágenes de linfocitos normales y reactivos, y de varios tipos de células linfoides neoplásicas circulantes en sangre periférica en algunos tipos de neoplasias linfoides B maduras, usando métodos de procesamiento digital de imágenes. Este objetivo sigue dos direcciones: (1) con una orientación propia de la ingeniería y la matemática de soporte, se desarrollan las metodologías transversales y las herramientas de software para su implementación; y (2) con un enfoque orientado al diagnóstico desde el laboratorio clínico, se construye y se valida un prototipo de un sistema cuya entrada es un conjunto de imágenes de células patológicas de pacientes analizados de forma individual, obtenidas mediante microscopía y cámara digital, y cuya salida es la clasificación automática en uno de los grupos de las distintas patologías incluidas en el sistema. Esta tesis es el resultado de la evolución de varios trabajos, comenzando con una discriminación entre linfocitos normales y dos tipos de células linfoides neoplásicas, y terminando con el diseño de un sistema para el reconocimiento automático de linfocitos normales y reactivos, y cinco tipos de células linfoides neoplásicas. Todo este trabajo involucra el desarrollo de una metodología de segmentación robusta usando agrupamiento por color, la cual es capaz de separar tres regiones de interés: la célula, el núcleo y la zona externa alrededor de la célula. Se desarrolla una descripción completa de la célula linfoide mediante la extracción de descriptores relacionados con el tamaño, la forma, la textura y el color. Para reducir la complejidad del proceso, se realiza una selección de descriptores usando teoría de la información. Posteriormente, se implementan varios clasificadores para reconocer automáticamente diferentes tipos de células linfoides. Los mejores resultados de clasificación se logran utilizando máquinas de soporte vectorial con núcleo de base radial. La metodología desarrollada, que combina conocimientos médicos, matemáticos y de ingeniería, es el primer paso para el diseño de una herramienta práctica de soporte al diagnóstico hematológico en un futuro cercano