CoolBox: A flexible toolkit for visual analysis of genomics data

We developed CoolBox, an open source toolkit for visual analysis of genomics data, which is highly compatible with the Python ecosystem, easy to use and highly customizable with a well-designed user interface. It can be used in various visualization situations like a Swiss army knife, for example, to produce high-quality genome track plots or fetch common used genomic data files with a Python script or command line, interactively explore genomic data within Jupyter environment or web browser. Moreover, owing to the highly extensible API design, users can customize their own tracks without difficulty, which can greatly facilitate analytical, comparative genomic data visualization tasks.

Tersect: a set theoretical utility for exploring sequence variant data

Summary Comparing genomic features among a large panel of individuals across the same species is considered nowadays a core part of the bioinformatics analyses. This typically involves a series of complex theoretical expressions to compare, intersect, extract symmetric differences between individuals within a large set of genotypes. Several publically available tools are capable of performing such tasks; however, due to the sheer size of variants being queried, such tasks can be computationally expensive with a runtime ranging from few minutes up to several hours depending on the dataset size. This makes existing tools unsuitable for interactive data query or as part of genomic data visualization platforms such as genome browsers. Tersect is a lightweight, high-performance command-line utility which interprets and applies flexible set theoretical expressions to sets of sequence variant data. It can be used both for interactive data exploration and as part of a larger pipeline thanks to its highly optimized storage and indexing algorithms for variant data. Availability and implementation Tersect was implemented in C and released under the MIT license. Tersect is freely available at https://github.com/tomkurowski/tersect. Supplementary information Supplementary data are available at Bioinformatics online.

CoolBox: a interactive genomic data explorer for Jupyter Notebook

SummaryCoolBox is a Python package for interactive genomic data exploration based on Jupyter notebook. It provides a ggplot2-like Application Programming Interface (API) for genomic data visualization, and a Jupyter/ipywidgets based Graphical User Interface (GUI) for interactive data exploration. CoolBox is a versatile multi-omics explorer supporting most types of data formats generated by various sequencing technologies like RNA-Seq, ChIP-Seq, ChIA-PET and Hi-C.Availability and implementationCoolBox is purely implemented with Python, and the GUI widget in Jupyter notebook is based on the ipywidgets package. It is open-source and available under GPLv3 license at https://github.com/GangCaoLab/CoolBox.

Epiviz Web Components: reusable and extensible component library to visualize functional genomic datasets

Interactive and integrative data visualization tools and libraries are integral to exploration and analysis of genomic data. Web based genome browsers allow integrative data exploration of a large number of data sets for a specific region in the genome. Currently available web-based genome browsers are developed for specific use cases and datasets, therefore integration and extensibility of the visualizations and the underlying libraries from these tools is a challenging task. Genomic data visualization and software libraries that enable bioinformatic researchers and developers to implement customized genomic data viewers and data analyses for their application are much needed. Using recent advances in core web platform APIs and technologies including Web Components, we developed the Epiviz Component Library, a reusable and extensible data visualization library and application framework for genomic data. Epiviz Components can be integrated with most JavaScript libraries and frameworks designed for HTML. To demonstrate the ease of integration with other frameworks, we developed an R/Bioconductor epivizrChart package, that provides interactive, shareable and reproducible visualizations of genomic data objects in R, Shiny and also create standalone HTML documents. The component library is modular by design, reusable and natively extensible and therefore simplifies the process of managing and developing bioinformatic applications.

The Representation of Neural Data Using Visualization

Currently, the focus of research within Information Visualization is steering towards genomic data visualization due to the level of activity that the Human Genome Project has generated. However, the Human Brain project, renowned within Neuroinformatics, is equally challenging and exciting. Its main aim is to increase current understanding of brain function such as memory, learning, attention, emotions and consciousness. It is understood that this task will require the ‘integration of information from the level of the gene to the level of behaviour'. The work presented in this paper focuses on the visualization of neural data. More specifically, the data being analysed is multi-dimensional spike train data. Traditional methods, such as the ‘raster plot’ and the ‘cross-correlogram', are still useful but they do not scale up for larger assemblies of neurons. In this paper, a new innovative method called the Tunnel is defined. Its design is based on the principles of Information Visualization; overview the data, zoom and filter data, data details on demand. The features of this visualization environment are described. This includes data filtering, navigation and a ‘flat map’ overview facility. Additionally, a ‘coincidence overlay map’ is presented. This map washes the Tunnel with colour, which encodes the coincidence of spikes.