Chareshneu Aliaksei, Cantara Alessio, Tichý Dominick, Sehnal David
National Centre for Biomolecular Research, Faculty of Science, Masaryk University, Brno, Czech Republic.
The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint first authors.
Curr Protoc. 2024 Dec;4(12):e70070. doi: 10.1002/cpz1.70070.
Ever-increasing availability of experimental volumetric data (e.g., in .ccp4, .mrc, .map, .rec, .zarr, .ome.tif formats) and advances in segmentation software (e.g., Amira, Segger, IMOD) and formats (e.g., .am, .seg, .mod, etc.) have led to a demand for efficient web-based visualization tools. Despite this, current solutions remain scarce, hindering data interpretation and dissemination. Previously, we introduced Mol* Volumes & Segmentations (Mol* VS), a web application for the visualization of volumetric, segmentation, and annotation data (e.g., semantically relevant information on biological entities corresponding to individual segmentations such as Gene Ontology terms or PDB IDs). However, this lacked important features such as the ability to edit annotations (e.g., assigning user-defined descriptions of a segment) and seamlessly share visualizations. Additionally, setting up Mol* VS required a substantial programming background. This article presents an updated version, Mol* VS 2.0, that addresses these limitations. As part of Mol* VS 2.0, we introduce the Annotation Editor, a user-friendly graphical interface for editing annotations, and the Volumes & Segmentations Toolkit (VSToolkit) for generating shareable files with visualization data. The outlined protocols illustrate the utilization of Mol* VS 2.0 for visualization of volumetric and segmentation data across various scales, showcasing the progress in the field of molecular complex visualization. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: VSToolkit-setting up and visualizing a user-constructed Mol* VS 2.0 database entry Basic Protocol 2: VSToolkit-visualizing multiple time frames and volume channels Support Protocol 1: Example: Adding database entry idr-13457537 Alternate Protocol 1: Local-server-and-viewer-visualizing multiple time frames and volume channels Support Protocol 2: Addition of database entry custom-tubhiswt Basic Protocol 3: VSToolkit-visualizing a specific channel and time frame Basic Protocol 4: VSToolkit-visualizing geometric segmentation Basic Protocol 5: VSToolkit-visualizing lattice segmentations Alternate Protocol 2: "Local-server-and-viewer"-visualizing lattice segmentations Basic Protocol 6: "Local-server-and-viewer"-visualizing multiple volume channels Support Protocol 3: Deploying a server API Support Protocol 4: Hosting Mol* viewer with VS extension 2.0 Support Protocol 5: Example: Addition of database entry empiar-11756 Support Protocol 6: Example: Addition of database entry emd-1273 Support Protocol 7: Editing annotations Support Protocol 8: Addition of database entry idr-5025553.
实验性体积数据(例如.ccp4、.mrc、.map、.rec、.zarr、.ome.tif格式)的可得性不断提高,以及分割软件(例如Amira、Segger、IMOD)和格式(例如.am、.seg、.mod等)的进步,引发了对高效的基于网络的可视化工具的需求。尽管如此,当前的解决方案仍然稀缺,这阻碍了数据的解释和传播。此前,我们推出了Mol* Volumes & Segmentations(Mol* VS),这是一个用于可视化体积、分割和注释数据的网络应用程序(例如与各个分割相对应的生物实体的语义相关信息,如基因本体术语或PDB ID)。然而,它缺乏一些重要功能,如编辑注释的能力(例如为一个分割分配用户定义的描述)以及无缝共享可视化结果。此外,设置Mol* VS需要扎实的编程背景。本文介绍了一个更新版本,即Mol* VS 2.0,它解决了这些限制。作为Mol* VS 2.0的一部分,我们引入了注释编辑器,这是一个用于编辑注释的用户友好型图形界面,以及用于生成带有可视化数据的可共享文件的体积与分割工具包(VSToolkit)。所概述的方案展示了如何利用Mol* VS 2.0在各种尺度上可视化体积和分割数据,突显了分子复合物可视化领域的进展。© 2024作者。由Wiley Periodicals LLC出版的《Current Protocols》。基本方案1:VSToolkit - 设置并可视化用户构建的Mol* VS 2.0数据库条目 基本方案2:VSToolkit - 可视化多个时间帧和体积通道 支持方案1:示例:添加数据库条目idr - 13457537 替代方案1:本地服务器和查看器 - 可视化多个时间帧和体积通道 支持方案2:添加数据库条目custom - tubhiswt 基本方案3:VSToolkit - 可视化特定通道和时间帧 基本方案4:VSToolkit - 可视化几何分割 基本方案5:VSToolkit - 可视化晶格分割 替代方案2:“本地服务器和查看器” - 可视化晶格分割 基本方案6:“本地服务器和查看器” - 可视化多个体积通道 支持方案3:部署服务器应用程序编程接口 支持方案4:托管带有VS扩展2.0的Mol*查看器 支持方案5:示例:添加数据库条目empiar - 11756 支持方案6:示例:添加数据库条目emd - 1273 支持方案7:编辑注释 支持方案8:添加数据库条目idr - 5025553。