🍩 Database of Original & Non-Theoretical Uses of Topology

(found 3 matches in 0.001292s)

  1. Topology of Viral Evolution (2013)

    Joseph Minhow Chan, Gunnar Carlsson, Raul Rabadan
    Abstract The tree structure is currently the accepted paradigm to represent evolutionary relationships between organisms, species or other taxa. However, horizontal, or reticulate, genomic exchanges are pervasive in nature and confound characterization of phylogenetic trees. Drawing from algebraic topology, we present a unique evolutionary framework that comprehensively captures both clonal and reticulate evolution. We show that whereas clonal evolution can be summarized as a tree, reticulate evolution exhibits nontrivial topology of dimension greater than zero. Our method effectively characterizes clonal evolution, reassortment, and recombination in RNA viruses. Beyond detecting reticulate evolution, we succinctly recapitulate the history of complex genetic exchanges involving more than two parental strains, such as the triple reassortment of H7N9 avian influenza and the formation of circulating HIV-1 recombinants. In addition, we identify recurrent, large-scale patterns of reticulate evolution, including frequent PB2-PB1-PA-NP cosegregation during avian influenza reassortment. Finally, we bound the rate of reticulate events (i.e., 20 reassortments per year in avian influenza). Our method provides an evolutionary perspective that not only captures reticulate events precluding phylogeny, but also indicates the evolutionary scales where phylogenetic inference could be accurate.

  2. Topology Identifies Emerging Adaptive Mutations in SARS-CoV-2 (2021)

    Michael Bleher, Lukas Hahn, Juan Angel Patino-Galindo, Mathieu Carriere, Ulrich Bauer, Raul Rabadan, Andreas Ott
    Abstract The COVID-19 pandemic has lead to a worldwide effort to characterize its evolution through the mapping of mutations in the genome of the coronavirus SARS-CoV-2. Ideally, one would like to quickly identify new mutations that could confer adaptive advantages (e.g. higher infectivity or immune evasion) by leveraging the large number of genomes. One way of identifying adaptive mutations is by looking at convergent mutations, mutations in the same genomic position that occur independently. However, the large number of currently available genomes precludes the efficient use of phylogeny-based techniques. Here, we establish a fast and scalable Topological Data Analysis approach for the early warning and surveillance of emerging adaptive mutations based on persistent homology. It identifies convergent events merely by their topological footprint and thus overcomes limitations of current phylogenetic inference techniques. This allows for an unbiased and rapid analysis of large viral datasets. We introduce a new topological measure for convergent evolution and apply it to the GISAID dataset as of February 2021, comprising 303,651 high-quality SARS-CoV-2 isolates collected since the beginning of the pandemic. We find that topologically salient mutations on the receptor-binding domain appear in several variants of concern and are linked with an increase in infectivity and immune escape, and for many adaptive mutations the topological signal precedes an increase in prevalence. We show that our method effectively identifies emerging adaptive mutations at an early stage. By localizing topological signals in the dataset, we extract geo-temporal information about the early occurrence of emerging adaptive mutations. The identification of these mutations can help to develop an alert system to monitor mutations of concern and guide experimentalists to focus the study of specific circulating variants.

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  3. Topological Descriptors of Histology Images (2014)

    Nikhil Singh, Heather D. Couture, J. S. Marron, Charles Perou, Marc Niethammer
    Abstract The purpose of this study is to investigate architectural characteristics of cell arrangements in breast cancer histology images. We propose the use of topological data analysis to summarize the geometric information inherent in tumor cell arrangements. Our goal is to use this information as signatures that encode robust summaries of cell arrangements in tumor tissue as captured through histology images. In particular, using ideas from algebraic topology we construct topological descriptors based on cell nucleus segmentations such as persistency charts and Betti sequences. We assess their performance on the task of discriminating the breast cancer subtypes Basal, Luminal A, Luminal B and HER2. We demonstrate that the topological features contain useful complementary information to image-appearance based features that can improve discriminatory performance of classifiers.