A Primer on Persistent Homology of Finite Metric Spaces.

Topological data analysis (TDA) is a relatively new area of research related to importing classical ideas from topology into the realm of data analysis. Under the umbrella term TDA, there falls, in particular, the notion of persistent homology PH, which can be described in a nutshell, as the study of scale-dependent homological invariants of datasets. In these notes, we provide a terse self-contained description of the main ideas behind the construction of persistent homology as an invariant feature of datasets, and its stability to perturbations.

The importance of forgetting: Limiting memory improves recovery of topological characteristics from neural data.

We develop of a line of work initiated by Curto and Itskov towards understanding the amount of information contained in the spike trains of hippocampal place cells via topology considerations. Previously, it was established that simply knowing which groups of place cells fire together in an animal's hippocampus is sufficient to extract the global topology of the animal's physical environment. We model a system where collections of place cells group and ungroup according to short-term plasticity rules. In particular, we obtain the surprising result that in experiments with spurious firing, the accuracy of the extracted topological information decreases with the persistence (beyond a certain regime) of the cell groups. This suggests that synaptic transience, or forgetting, is a mechanism by which the brain counteracts the effects of spurious place cell activity.

A Topological Model of the Hippocampal Cell Assembly Network.

It is widely accepted that the hippocampal place cells' spiking activity produces a cognitive map of space. However, many details of this representation's physiological mechanism remain unknown. For example, it is believed that the place cells exhibiting frequent coactivity form functionally interconnected groups-place cell assemblies-that drive readout neurons in the downstream networks. However, the sheer number of coactive combinations is extremely large, which implies that only a small fraction of them actually gives rise to cell assemblies. The physiological processes responsible for selecting the winning combinations are highly complex and are usually modeled via detailed synaptic and structural plasticity mechanisms. Here we propose an alternative approach that allows modeling the cell assembly network directly, based on a small number of phenomenological selection rules. We then demonstrate that the selected population of place cell assemblies correctly encodes the topology of the environment in biologically plausible time, and may serve as a schematic model of the hippocampal network.

Topological analysis of population activity in visual cortex.

Information in the cortex is thought to be represented by the joint activity of neurons. Here we describe how fundamental questions about neural representation can be cast in terms of the topological structure of population activity. A new method, based on the concept of persistent homology, is introduced and applied to the study of population activity in primary visual cortex (V1). We found that the topological structure of activity patterns when the cortex is spontaneously active is similar to those evoked by natural image stimulation and consistent with the topology of a two sphere. We discuss how this structure could emerge from the functional organization of orientation and spatial frequency maps and their mutual relationship. Our findings extend prior results on the relationship between spontaneous and evoked activity in V1 and illustrates how computational topology can help tackle elementary questions about the representation of information in the nervous system.

Implicit brain imaging.

We describe how implicit surface representations can be used to solve fundamental problems in brain imaging. This kind of representation is not only natural following the state-of-the-art segmentation algorithms reported in the literature to extract the different brain tissues, but it is also, as shown in this paper, the most appropriate one from the computational point of view. Examples are provided for finding constrained special curves on the cortex, such as sulcal beds, regularizing surface-based measures, such as cortical thickness, and for computing warping fields between surfaces such as the brain cortex. All these result from efficiently solving partial differential equations (PDEs) and variational problems on surfaces represented in implicit form. The implicit framework avoids the need to construct intermediate mappings between 3-D anatomical surfaces and parametric objects such planes or spheres, a complex step that introduces errors and is required by many other cortical processing approaches.