Complex network topologies represent the necessary substrate to support complex brain functions. In this work, we reviewed in vitro neuronal networks coupled to Micro-Electrode Arrays (MEAs) as biological substrate. Networks of dissociated neurons developing in vitro and coupled to MEAs, represent a valid experimental model for studying the mechanisms governing the formation, organization and conservation of neuronal cell assemblies. In this review, we present some examples of the use of statistical Cluster Coefficients and Small World indices to infer topological rules underlying the dynamics exhibited by homogeneous and engineered neuronal networks.

Functional-effective connectivity and network topology are nowadays key issues for studying brain physiological functions and pathologies. Inferring neuronal connectivity from electrophysiological recordings presents open challenges and unsolved problems. In this work, we present a cross-correlation based method for reliably estimating not only excitatory but also inhibitory links, by analyzing multi-unit spike activity from large-scale neuronal networks. The method is validated by means of realistic simulations of large-scale neuronal populations. New results related to functional connectivity estimation and network topology identification obtained by experimental electrophysiological recordings from high-density and large-scale (i.e., 4096 electrodes) microtransducer arrays coupled to in vitro neural populations are presented. Specifically, we show that: (i) functional inhibitory connections are accurately identified in in vitro cortical networks, providing that a reasonable firing rate and recording length are achieved; (ii) small-world topology, with scale-free and rich-club features are reliably obtained, on condition that a minimum number of active recording sites are available. The method and procedure can be directly extended and applied to in vivo multi-units brain activity recordings.

Our results support the idea that partial correlation is a good method for connectivity studies and can be applied to derive topological and structural features of neuronal assemblies.

Liver cancer is one of the leading causes of cancer deaths in Asia and Africa. It is caused by the Hepatocellular carcinoma (HCC) in almost 90% of all cases. HCC is a malignant tumor and the most common histological type of the primary liver cancers. The detection and evaluation of viable tumor regions in HCC present an important clinical significance since it is a key step to assess response of chemoradiotherapy and tumor cell proportion in genetic tests. Recent advances in computer vision, digital pathology and microscopy imaging enable automatic histopathology image analysis for cancer diagnosis. In this paper, we present a multi-resolution deep learning model HistoCAE for viable tumor segmentation in whole-slide liver histopathology images. We propose convolutional autoencoder (CAE) based framework with a customized reconstruction loss function for image reconstruction, followed by a classification module to classify each image patch as tumor versus non-tumor. The resulting patch-based prediction results are spatially combined to generate the final segmentation result for each WSI. Additionally, the spatially organized encoded feature map derived from small image patches is used to compress the gigapixel whole-slide images. Our proposed model presents superior performance to other benchmark models with extensive experiments, suggesting its efficacy for viable tumor area segmentation with liver whole-slide images.

Nowadays, the use of in vitro reduced models of neuronal networks to investigate the interplay between structural-functional connectivity and the emerging collective dynamics is a widely accepted approach. In this respect, a relevant advance for this kind of studies has been given by the recent introduction of high-density large-scale Micro-Electrode Arrays (MEAs) which have favored the mapping of functional connections and the recordings of the neuronal electrical activity. Although, several toolboxes have been implemented to characterize network dynamics and derive functional links, no specifically dedicated software for the management of huge amount of data and direct estimation of functional connectivity maps has been developed. toolconnect offers the implementation of up to date algorithms and a user-friendly Graphical User Interface (GUI) to analyze recorded data from large scale networks. It has been specifically conceived as a computationally efficient open-source software tailored to infer functional connectivity by analyzing the spike trains acquired from in vitro networks coupled to MEAs. In the current version, toolconnect implements correlation- (cross-correlation, partial-correlation) and information theory (joint entropy, transfer entropy) based core algorithms, as well as useful and practical add-ons to visualize functional connectivity graphs and extract some topological features. In this work, we present the software, its main features and capabilities together with some demonstrative applications on hippocampal recordings.