Biological networks describe complex relationships in biological systems, which represent biological entities as vertices and their underlying connectivity as edges. Ideally, for a complete analysis of such systems, domain experts need to visually integrate multiple sources of heterogeneous data , and visually, as well as numerically, probe said data in order to explore or validate (mechanistic) hypotheses. Such visual analyses require the coming together of biological domain experts, bioinformaticians, as well as network scientists to create useful visualization tools. Owing to the underlying graph data becoming ever larger and more complex, the visual representation of such biological networks has become challenging in its own right. This introduction and survey aims to describe the current state of biological network visualization in order to identify scientific gaps for visualization experts, network scientists, bioinformaticians, and domain experts, such as biologists, or biochemists, alike. Specifically, we revisit the classic visualization pipeline, upon which we base this paper’s taxonomy and structure, which in turn forms the basis of our literature classification. This pipeline describes the process of visualizing data, starting with the raw data itself, through the construction of data tables, to the actual creation of visual structures and views, as a function of task-driven user interaction. Literature was systematically surveyed using API-driven querying where possible, and the collected papers were manually read and categorized based on the identified sub-components of this visualization pipeline’s individual steps. From this survey, we highlight a number of exemplary visualization tools from multiple biological sub-domains in order to explore how they adapt these discussed techniques and why. Additionally, this taxonomic classification of the collected set of papers allows us to identify existing gaps in biological network visualization practices. We finally conclude this report with a list of open challenges and potential research directions. Examples of such gaps include (i) the overabundance of visualization tools using schematic or straight-line node-link diagrams, despite the availability of powerful alternatives, or (ii) the lack of visualization tools that also integrate more advanced network analysis techniques beyond basic graph descriptive statistics.

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/ .

Relational information between different types of entities is often modelled by a multilayer network (MLN) - a network with subnetworks represented by layers. The layers of an MLN can be arranged in different ways in a visual representation, however, the impact of the arrangement on the readability of the network is an open question. Therefore, we studied this impact for several commonly occurring tasks related to MLN analysis. Additionally, layer arrangements with a dimensionality beyond 2D, which are common in this scenario, motivate the use of stereoscopic displays. We ran a human subject study utilising a Virtual Reality headset to evaluate 2D, 2.5D, and 3D layer arrangements. The study employs six analysis tasks that cover the spectrum of an MLN task taxonomy, from path finding and pattern identification to comparisons between and across layers. We found no clear overall winner. However, we explore the task-to-arrangement space and derive empirical-based recommendations on the effective use of 2D, 2.5D, and 3D layer arrangements for MLNs.

Molecular docking is a key technique in various fields like structural biology, medicinal chemistry, and biotechnology. It is widely used for virtual screening during drug discovery, computer-assisted drug design, and protein engineering. A general molecular docking process consists of the target and ligand selection, their preparation, and the docking process itself, followed by the evaluation of the results. However, the most commonly used docking software provides no or very basic evaluation possibilities. Scripting and external molecular viewers are often used, which are not designed for an efficient analysis of docking results. Therefore, we developed InVADo, a comprehensive interactive visual analysis tool for large docking data. It consists of multiple linked 2D and 3D views. It filters and spatially clusters the data, and enriches it with post-docking analysis results of protein-ligand interactions and functional groups, to enable well-founded decision-making. In an exemplary case study, domain experts confirmed that InVADo facilitates and accelerates the analysis workflow. They rated it as a convenient, comprehensive, and feature-rich tool, especially useful for virtual screening.

Abstract We present an approach for the visual analysis of multi‐omics data obtained using high‐throughput methods. The term “omics” denotes measurements of different types of biologically relevant molecules like the products of gene transcription (transcriptomics) or the abundance of proteins (proteomics). Current popular visualization approaches often only support analyzing each of these omics separately. This, however, disregards the interconnectedness of different biologically relevant molecules and processes. Consequently, it describes the actual events in the organism suboptimally or only partially. Our visual analytics approach for multi‐omics data provides a comprehensive overview and details‐on‐demand by integrating the different omics types in multiple linked views. To give an overview, we map the measurements to known biological pathways and use a combination of a clustered network visualization, glyphs, and interactive filtering. To ensure the effectiveness and utility of our approach, we designed it in close collaboration with domain experts and assessed it using an exemplary workflow with real‐world transcriptomics, proteomics, and lipidomics measurements from mice.

Abstract We present an approach for visual analysis of high‐dimensional measurement data with varying sampling rates as routinely recorded in intensive care units. In intensive care, most assessments not only depend on one single measurement but a plethora of mixed measurements over time. Even for trained experts, efficient and accurate analysis of such multivariate data remains a challenging task. We present a linked‐view post hoc visual analytics application that reduces data complexity by combining projection‐based time curves for overview with small multiples for details on demand. Our approach supports not only the analysis of individual patients but also of ensembles by adapting existing techniques using non‐parametric statistics. We evaluated the effectiveness and acceptance of our approach through expert feedback with domain scientists from the surgical department using real‐world data: a post‐surgery study performed on a porcine surrogate model to identify parameters suitable for diagnosing and prognosticating the volume state, and clinical data from a public database. The results show that our approach allows for detailed analysis of changes in patient state while also summarizing the temporal development of the overall condition.