Abstract Visualizing small‐world networks such as protein‐protein interaction networks or social networks often leads to visual clutter and limited interpretability. To overcome these problems, we presentProtEGOnist, a visualization approach designed to explore small‐world networks.ProtEGOnistvisualizes networks using ego‐graphs that represent local neighborhoods. Ego‐graphs are visualized in an aggregated state as a glyph where the size encodes the size of the neighborhood and in a detailed version where the original network nodes can be explored. The ego‐graphs are arranged in an ego‐graph network, where edges encode similarity using the Jaccard index. Our design aims to reduce visual complexity and clutter while enabling detailed exploration and facilitating the discovery of meaningful patterns. To achieve this, our approach offers a network overview using ego‐graphs, a radar chart for a one‐to‐many ego‐graph comparison and meta‐data integration, and detailed ego‐graph subnetworks for interactive exploration. We demonstrate the applicability of our approach on a co‐author network and two different protein‐protein interaction networks. A web‐based prototype ofProtEGOnistcan be accessed online at https://protegonist-tuevis.cs.uni-tuebingen.de/ .

In this paper, we present two approaches and algorithms that adapt areas of interest (AOI) or regions of interest (ROI), respectively, to the eye tracking data quality and classification task. The first approach uses feature importance in a greedy way and grows or shrinks AOIs in all directions. The second approach is an extension of the first approach, which divides the AOIs into areas and calculates a direction of growth, i.e. a gradient. Both approaches improve the classification results considerably in the case of generalized AOIs, but can also be used for qualitative analysis. In qualitative analysis, the algorithms presented allow the AOIs to be adapted to the data, which means that errors and inaccuracies in eye tracking data can be better compensated for. A good application example is abstract art, where manual AOIs annotation is hardly possible, and data-driven approaches are mainly used for initial AOIs.

In this paper, we present two approaches and algorithms that adapt areas of interest. We present a new deep neural network (DNN) that can be used to directly determine gaze position using EEG data. EEG-based eye tracking is a new and difficult research topic in the field of eye tracking, but it provides an alternative to image-based eye tracking with an input data set comparable to conventional image processing. The presented DNN exploits spatial dependencies of the EEG signal and uses convolutions similar to spatial filtering, which is used for preprocessing EEG signals. By this, we improve the direct gaze determination from the EEG signal compared to the state of the art by 3.5 cm MAE (Mean absolute error), but unfortunately still do not achieve a directly applicable system, since the inaccuracy is still significantly higher compared to image-based eye trackers.

Abstract Analysis pipelines in genomics, transcriptomics, and proteomics commonly produce lists of genes, e.g., differentially expressed genes. Often these lists overlap only partly or not at all and contain too many genes for manual comparison. However, using background knowledge, such as the functional annotations of the genes, the lists can be abstracted to functional terms. One approach is to run Gene Ontology (GO) enrichment analyses to determine over‐ and/or underrepresented functions for every list of genes. Due to the hierarchical structure of the Gene Ontology, lists of enriched GO terms can contain many closely related terms, rendering the lists still long, redundant, and difficult to interpret for researchers. In this paper, we present GO‐Compass (Gene Ontology list comparison using Semantic Similarity), a visual analytics tool for the dispensability reduction and visual comparison of lists of GO terms. For dispensability reduction, we adapted the RE‐VIGO algorithm, a summarization method based on the semantic similarity of GO terms, to perform hierarchical dispensability clustering on multiple lists. In an interactive dashboard, GO‐Compass offers several visualizations for the comparison and improved interpretability of GO terms lists. The hierarchical dispensability clustering is visualized as a tree, where users can interactively filter out dispensable GO terms and create flat clusters by cutting the tree at a chosen dispensability. The flat clusters are visualized in animated treemaps and are compared using a correlation heatmap, UpSet plots, and bar charts. With two use cases on published datasets from different omics domains, we demonstrate the general applicability and effectiveness of our approach. In the first use case, we show how the tool can be used to compare lists of differentially expressed genes from a transcriptomics pipeline and incorporate gene information into the analysis. In the second use case using genomics data, we show how GO‐Compass facilitates the analysis of many hundreds of GO terms. For qualitative evaluation of the tool, we conducted feedback sessions with five domain experts and received positive comments. GO‐Compass is part of the Tue‐Vis Visualization Server as a web application available at https://go‐compass‐tuevis.cs.uni‐tuebingen.de/

A growing number of longitudinal cohort studies are generating data with extensive patient observations across multiple timepoints. Such data offers promising opportunities to better understand the progression of diseases. However, these observations are usually treated as general events in existing visual analysis tools. As a result, their capabilities in modeling disease progression are not fully utilized. To fill this gap, we designed and implemented ThreadStates, an interactive visual analytics tool for the exploration of longitudinal patient cohort data. The focus of ThreadStates is to identify the states of disease progression by learning from observation data in a human-in-the-loop manner. We propose a novel Glyph Matrix design and combine it with a scatter plot to enable seamless identification, observation, and refinement of states. The disease progression patterns are then revealed in terms of state transitions using Sankey-based visualizations. We employ sequence clustering techniques to find patient groups with distinctive progression patterns, and to reveal the association between disease progression and patient-level features. The design and development were driven by a requirement analysis and iteratively refined based on feedback from domain experts over the course of a 10-month design study. Case studies and expert interviews demonstrate that ThreadStates can successively summarize disease states, reveal disease progression, and compare patient groups.

Genomic data visualization is essential for interpretation and hypothesis generation as well as a valuable aid in communicating discoveries. Visual tools bridge the gap between algorithmic approaches and the cognitive skills of investigators. Addressing this need has become crucial in genomics, as biomedical research is increasingly data-driven and many studies lack well-defined hypotheses. A key challenge in data-driven research is to discover unexpected patterns and to formulate hypotheses in an unbiased manner in vast amounts of genomic and other associated data. Over the past two decades, this has driven the development of numerous data visualization techniques and tools for visualizing genomic data. Based on a comprehensive literature survey, we propose taxonomies for data, visualization, and tasks involved in genomic data visualization. Furthermore, we provide a comprehensive review of published genomic visualization tools in the context of the proposed taxonomies.