🍩 Database of Original & Non-Theoretical Uses of Topology
(found 4 matches in 0.001172s)
-
-
Inferring COVID-19 Biological Pathways From Clinical Phenotypes via Topological Analysis (2021)
Negin Karisani, Daniel E. Platt, Saugata Basu, Laxmi ParidaAbstract
COVID-19 has caused thousands of deaths around the world and also resulted in a large international economic disruption. Identifying the pathways associated with this illness can help medical researchers to better understand the properties of the condition. This process can be carried out by analyzing the medical records. It is crucial to develop tools and models that can aid researchers with this process in a timely manner. However, medical records are often unstructured clinical notes, and this poses significant challenges to developing the automated systems. In this article, we propose a pipeline to aid practitioners in analyzing clinical notes and revealing the pathways associated with this disease. Our pipeline relies on topological properties and consists of three steps: 1) pre-processing the clinical notes to extract the salient concepts, 2) constructing a feature space of the patients to characterize the extracted concepts, and finally, 3) leveraging the topological properties to distill the available knowledge and visualize the result. Our experiments on a publicly available dataset of COVID-19 clinical notes testify that our pipeline can indeed extract meaningful pathways. -
Classification of COVID-19 via Homology of CT-SCAN (2021)
Sohail Iqbal, H. Fareed Ahmed, Talha Qaiser, Muhammad Imran Qureshi, Nasir RajpootAbstract
In this worldwide spread of SARS-CoV-2 (COVID-19) infection, it is of utmost importance to detect the disease at an early stage especially in the hot spots of this epidemic. There are more than 110 Million infected cases on the globe, sofar. Due to its promptness and effective results computed tomography (CT)-scan image is preferred to the reverse-transcription polymerase chain reaction (RT-PCR). Early detection and isolation of the patient is the only possible way of controlling the spread of the disease. Automated analysis of CT-Scans can provide enormous support in this process. In this article, We propose a novel approach to detect SARS-CoV-2 using CT-scan images. Our method is based on a very intuitive and natural idea of analyzing shapes, an attempt to mimic a professional medic. We mainly trace SARS-CoV-2 features by quantifying their topological properties. We primarily use a tool called persistent homology, from Topological Data Analysis (TDA), to compute these topological properties. We train and test our model on the "SARS-CoV-2 CT-scan dataset" i̧tep\soares2020sars\, an open-source dataset, containing 2,481 CT-scans of normal and COVID-19 patients. Our model yielded an overall benchmark F1 score of \$99.42\% \$, accuracy \$99.416\%\$, precision \$99.41\%\$, and recall \$99.42\%\$. The TDA techniques have great potential that can be utilized for efficient and prompt detection of COVID-19. The immense potential of TDA may be exploited in clinics for rapid and safe detection of COVID-19 globally, in particular in the low and middle-income countries where RT-PCR labs and/or kits are in a serious crisis. -
Determining Clinically Relevant Features in Cytometry Data Using Persistent Homology (2022)
Soham Mukherjee, Darren Wethington, Tamal K. Dey, Jayajit DasAbstract
Cytometry experiments yield high-dimensional point cloud data that is difficult to interpret manually. Boolean gating techniques coupled with comparisons of relative abundances of cellular subsets is the current standard for cytometry data analysis. However, this approach is unable to capture more subtle topological features hidden in data, especially if those features are further masked by data transforms or significant batch effects or donor-to-donor variations in clinical data. We present that persistent homology, a mathematical structure that summarizes the topological features, can distinguish different sources of data, such as from groups of healthy donors or patients, effectively. Analysis of publicly available cytometry data describing non-naïve CD8+ T cells in COVID-19 patients and healthy controls shows that systematic structural differences exist between single cell protein expressions in COVID-19 patients and healthy controls. We identify proteins of interest by a decision-tree based classifier, sample points randomly and compute persistence diagrams from these sampled points. The resulting persistence diagrams identify regions in cytometry datasets of varying density and identify protruded structures such as ‘elbows’. We compute Wasserstein distances between these persistence diagrams for random pairs of healthy controls and COVID-19 patients and find that systematic structural differences exist between COVID-19 patients and healthy controls in the expression data for T-bet, Eomes, and Ki-67. Further analysis shows that expression of T-bet and Eomes are significantly downregulated in COVID-19 patient non-naïve CD8+ T cells compared to healthy controls. This counter-intuitive finding may indicate that canonical effector CD8+ T cells are less prevalent in COVID-19 patients than healthy controls. This method is applicable to any cytometry dataset for discovering novel insights through topological data analysis which may be difficult to ascertain otherwise with a standard gating strategy or existing bioinformatic tools.Community Resources