🍩 Database of Original & Non-Theoretical Uses of Topology

(found 4 matches in 0.001642s)

  1. Raman Spectroscopy and Topological Machine Learning for Cancer Grading (2023)

    Francesco Conti, Mario D’Acunto, Claudia Caudai, Sara Colantonio, Raffaele Gaeta, Davide Moroni, Maria Antonietta Pascali
    Abstract In the last decade, Raman Spectroscopy is establishing itself as a highly promising technique for the classification of tumour tissues as it allows to obtain the biochemical maps of the tissues under investigation, making it possible to observe changes among different tissues in terms of biochemical constituents (proteins, lipid structures, DNA, vitamins, and so on). In this paper, we aim to show that techniques emerging from the cross-fertilization of persistent homology and machine learning can support the classification of Raman spectra extracted from cancerous tissues for tumour grading. In more detail, topological features of Raman spectra and machine learning classifiers are trained in combination as an automatic classification pipeline in order to select the best-performing pair. The case study is the grading of chondrosarcoma in four classes: cross and leave-one-patient-out validations have been used to assess the classification accuracy of the method. The binary classification achieves a validation accuracy of 81% and a test accuracy of 90%. Moreover, the test dataset has been collected at a different time and with different equipment. Such results are achieved by a support vector classifier trained with the Betti Curve representation of the topological features extracted from the Raman spectra, and are excellent compared with the existing literature. The added value of such results is that the model for the prediction of the chondrosarcoma grading could easily be implemented in clinical practice, possibly integrated into the acquisition system.

  2. The Shape of Cancer Relapse: Topological Data Analysis Predicts Recurrence in Paediatric Acute Lymphoblastic Leukaemia (2021)

    Salvador Chulián, Bernadette J. Stolz, Álvaro Martínez-Rubio, Cristina Blázquez Goñi, Juan F. Rodríguez Gutiérrez, Teresa Caballero Velázquez, Águeda Molinos Quintana, Manuel Ramírez Orellana, Ana Castillo Robleda, José Luis Fuster Soler, Alfredo Minguela Puras, María Victoria Martínez Sánchez, María Rosa, Víctor M. Pérez-García, Helen Byrne
    Abstract Acute Lymphoblastic Leukaemia (ALL) is the most frequent paediatric cancer. Modern therapies have improved survival rates, but approximately 15-20 % of patients relapse. At present, patients’ risk of relapse are assessed by projecting high-dimensional flow cytometry data onto a subset of biomarkers and manually estimating the shape of this reduced data. Here, we apply methods from topological data analysis (TDA), which quantify shape in data via features such as connected components and loops, to pre-treatment ALL datasets with known outcomes. We combine these fully unsupervised analyses with machine learning to identify features in the pre-treatment data that are prognostic for risk of relapse. We find significant topological differences between relapsing and non-relapsing patients and confirm the predictive power of CD10, CD20, CD38, and CD45. Further, we are able to use the TDA descriptors to predict patients who relapsed. We propose three prognostic pipelines that readily extend to other haematological malignancies. Teaser Topology reveals features in flow cytometry data which predict relapse of patients with acute lymphoblastic leukemia

  3. Histopathological Cancer Detection With Topological Signatures (2023)

    Ankur Yadav, Faisal Ahmed, Ovidiu Daescu, Reyhan Gedik, Baris Coskunuzer
    Abstract We present a transformative approach to histopathological cancer detection and grading by introducing a very powerful feature extraction method based on the latest topological data analysis tools. By analyzing the evolution of topological patterns in different color channels, we discovered that every tumor class leaves its own topological footprint in histopathological images, allowing to extract feature vectors that can be used to reliably identify tumor classes.Our topological signatures, even when combined with traditional machine learning methods, provide very fast and highly accurate results in various settings. While most DL models work well for one type of cancer, our model easily adapts to different scenarios, and consistently gives highly competitive results with the state-of-the-art models on benchmark datasets across multiple cancer types including bone, colon, breast, cervical (cytopathology), and prostate cancer. Unlike most DL models, our proposed Topo-ML model does not need any data augmentation or pre-processing steps and works perfectly on small datasets. The model is computationally very efficient, with end-to-end processing taking only a few hours for datasets consisting of thousands of images.

  4. Acute Lymphoblastic Leukemia Classification Using Persistent Homology (2024)

    Waqar Hussain Shah, Abdullah Baloch, Rider Jaimes-Reátegui, Sohail Iqbal, Syeda Rafia Fatima, Alexander N. Pisarchik
    Abstract Acute Lymphoblastic Leukemia (ALL) is a prevalent form of childhood blood cancer characterized by the proliferation of immature white blood cells that rapidly replace normal cells in the bone marrow. The exponential growth of these leukemic cells can be fatal if not treated promptly. Classifying lymphoblasts and healthy cells poses a significant challenge, even for domain experts, due to their morphological similarities. Automated computer analysis of ALL can provide substantial support in this domain and potentially save numerous lives. In this paper, we propose a novel classification approach that involves analyzing shapes and extracting topological features of ALL cells. We employ persistent homology to capture these topological features. Our technique accurately and efficiently detects and classifies leukemia blast cells, achieving a recall of 98.2% and an F1-score of 94.6%. This approach has the potential to significantly enhance leukemia diagnosis and therapy.