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Given a zigzag filtration, we want to find its barcode representatives, i.e., a compatible choice of bases for the homology groups that diagonalize the linear maps in the zigzag. To achieve this, we convert the input zigzag to a levelset zigzag of a real-valued function. This function generates a Mayer-Vietoris pyramid of spaces, which generates an infinite strip of homology groups. We call the origins of indecomposable (diamond) summands of this strip their apexes and give an algorithm to find representative cycles in these apexes from ordinary persistence computation. The resulting representatives map back to the levelset zigzag and thus yield barcode representatives for the input zigzag. Our algorithm for lifting a p-dimensional cycle from ordinary persistence to an apex representative takes O(p ⋅ m log m) time. From this we can recover zigzag representatives in time O(log m + C), where C is the size of the output. 

We extend the persistence algorithm, viewed as an algorithm computing the homology of a complex of free persistence or graded modules, to complexes of modules that are not free. We replace persistence modules by their presentations and develop an efficient algorithm to compute the homology of a complex of presentations. To deal with inputs that are not given in terms of presentations, we give an efficient algorithm to compute a presentation of a morphism of persistence modules. This allows us to compute persistent (co)homology of instances giving rise to complexes of non-free modules. Our methods lead to a new efficient algorithm for computing the persistent homology of simplicial towers and they enable efficient algorithms to compute the persistent homology of cosheaves over simplicial towers and cohomology of persistent sheaves on simplicial complexes. We also show that we can compute the cohomology of persistent sheaves over arbitrary finite posets by reducing the computation to a computation over simplicial complexes. 

Abstract Current complex prediction models are the result of fitting deep neural networks, graph convolutional networks or transducers to a set of training data. A key challenge with these models is that they are highly parameterized, which makes describing and interpreting the prediction strategies difficult. We use topological data analysis to transform these complex prediction models into a simplified topological view of the prediction landscape. The result is a map of the predictions that enables inspection of the model results with more specificity than dimensionality-reduction methods such as tSNE and UMAP. The methods scale up to large datasets across different domains. We present a case study of a transformer-based model previously designed to predict expression levels of a piece of DNA in thousands of genomic tracks. When the model is used to study mutations in theBRCA1gene, our topological analysis shows that it is sensitive to the location of a mutation and the exon structure ofBRCA1in ways that cannot be found with tools based on dimensionality reduction. Moreover, the topological framework offers multiple ways to inspect results, including an error estimate that is more accurate than model uncertainty. Further studies show how these ideas produce useful results in graph-based learning and image classification.