Automated segmentation and classification of unlabelled malaria parasites in red blood cells from phase contrast images

An automated method for detection of unlabelled malaria parasites in red blood cells is presented. From phase-constrast microscopy images of live red blood cells, the proposed algorithm segments red blood cells and classifies them into uninfected and infected cells. This approach can be used to o...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Mathew Athul Mangalathumannil
مؤلفون آخرون: Justin Dauwels
التنسيق: Theses and Dissertations
اللغة:English
منشور في: 2016
الموضوعات:
الوصول للمادة أونلاين:http://hdl.handle.net/10356/68682
الوسوم: إضافة وسم
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المؤسسة: Nanyang Technological University
اللغة: English
الوصف
الملخص:An automated method for detection of unlabelled malaria parasites in red blood cells is presented. From phase-constrast microscopy images of live red blood cells, the proposed algorithm segments red blood cells and classifies them into uninfected and infected cells. This approach can be used to observe the progression of malaria parasites through different stages as the algorithm presented can be used on unstained images. In related work, classification is performed on stained images. The image processing framework consists of image pre-processing, segmentation and classification of infected and uninfected cells from phase contrast images. Two segmentation methods; morphological operations and template matching, are applied and compared. To separate connected cells, a watershed algorithm is applied. The final goal of this project is to detect malaria infected cells from microscopic blood images at lowest magnification and then control the imaging system in the microscope to automatically zoom to monitor the infected cells. Manual detection of malaria from a cell sample is a very tedious and time consuming process. Using our methodology we are able to differentiate infected and non-infected cells automatically. Our approach also bypasses the need to stain the cell samples. This work can thus be implemented for fast, simple to execute and efficient diagnosis of malaria infected cells.