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Klasifikacija mielomskih celic na podlagi morfologije z globokim učenjem
ID Eržen, Ana (Author), ID Čehovin Zajc, Luka (Mentor) More about this mentor... This link opens in a new window, ID Kropivšek Brumat, Klara (Comentor)

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Abstract
Multipli mielom je heterogeno maligno obolenje, pri katerem klonalne plazemske celice izražajo imunoglobulinske lahke verige tipa κ ali λ. Namen diplomskega dela je raziskati, ali se morfološke značilnosti plazemskih celic razlikujejo glede na tip izražene lahke verige. Razvijemo pristop, ki temelji na konvolucijskih nevronskih mrežah z rezidualnimi povezavami (ResNet-18), za klasifikacijo celic na podlagi večkanalnih fluorescenčnih mikroskopskih slik. Rezultati kažejo, da razlike med κ- ali λ-pozitivnimi celicami niso stabilno izražene v morfološki slikovni reprezentaciji pri štirirazredni in dvorazredni formulaciji problema. Po reformulaciji naloge v trirazredno klasifikacijo optimizirana arhitektura z zmanjšano kapaciteto pri uporabi treh slikovnih kanalov doseže natančnost, ki kaže na biološko smiselno razločevanje razredov brez neposrednega klonalnega signala.

Language:Slovenian
Keywords:multipli mielom, globoko učenje, konvolucijske nevronske mreže, morfološka analiza, finozrnata klasifikacija
Work type:Bachelor thesis/paper
Organization:FRI - Faculty of Computer and Information Science
Year:2026
PID:20.500.12556/RUL-181299 This link opens in a new window
Publication date in RUL:31.03.2026
Views:152
Downloads:43
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Secondary language

Language:English
Title:Morphology-Based Classification of Myeloma Cells Using Deep Learning
Abstract:
Multiple myeloma is a heterogeneous malignant disease characterized by clonal plasma cells expressing either κ or λ immunoglobulin light chains. The aim of this thesis is to investigate whether morphological characteristics of plasma cells differ according to the expressed light-chain type. We develop a deep learning approach based on a residual convolutional neural network (ResNet-18) to classify cells using multi-channel fluorescence microscopy images. The results indicate that morphological differences between κ- and λ -positive cells are not stably represented in the image-based feature space under four-class and binary classification formulations. However, after reformulating the task as a three-class classification problem separating κ-positive cells, λ -positive cells, and non-clonal cells, an optimized reduced-capacity architecture achieves robust classification performance using three imaging channels, indicating biologically meaningful morphological differentiation independent of a direct clonal marker signal.

Keywords:multiple myeloma, deep learning, convolutional neural networks, morphological analysis, fine-grained classification

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