CIBR:BBSRC: Next generation collaborative annotation of genomes and synteny

基因组测序的物种数量正在迅速增加，并将继续这样做，在英国（达尔文生命之树项目）和地球上（地球生物基因组项目）正在进行的所有真核生物物种的测序项目。为了理解组装的基因组数据的重要特征，如蛋白质和非编码基因，需要识别和描述;这个一般过程称为注释。尽管自动注释基因组的方法取得了重大进展，但最准确的注释需要人工评估。然而，高昂的成本通常会阻止对单个物种进行手动注释（以及策划更新）。一个可扩展的替代方案是将手动工作导向参考数据集，并从更广泛的研究社区收集贡献。由此产生的高质量的注释，然后可以预测跨物种的基础上推断的同源性。用于注释的软件必须快速，灵活，易于不同社区的注释者（专业策展人，实验室生物学家或好奇的非专家）使用。 在目前可用的基因组注释软件平台中，Artemis和Apollo是最受欢迎的两个，已经广泛使用了20年。由桑格研究所开发的Artemis主要用于观察、注释和分析原核和真核微生物的基因组。Artemis的一个主要优势是它的同伴“Artemis比较工具”（ACT），它允许在发现和探索基因组保护的背景下创建或编辑基因结构。Artemis和ACT的一个主要限制是软件在大于几十兆字节的序列上性能很差。像Artemis一样，Apollo最初是一个桌面工具，但后来被重新设计为一个基于网络的工具，现在在一个共享服务器上运行，这样多个用户就可以同时浏览和创建同一个基因组的注释。Apollo可轻松处理任何大小的基因组，并可与多个并发用户进行良好的扩展。 该项目将整合Artemis和Apollo的最佳功能，以创建一个更高性能的注释平台。新的阿波罗将受益于现代化和模块化的架构，以实现协同开发和提高可持续性。Apollo还将通过与EMBL-EBI小组合作开发的新数据接口进行增强，以便可以跨服务器访问基因组比较数据，并在探索同线性的背景下进行注释。 新一代的注释工具将取代现有的Artemis和Apollo项目，并被集成到主要的基因组注释项目中，同时保留单个小规模用户的可用性。该奖项反映了NSF的法定使命，并通过使用基金会的知识价值和更广泛的影响审查标准进行评估，被认为值得支持。

The number of species with sequenced genomes is rising rapidly and will continue to do so with projects to sequence all eukaryotic species in the UK (Darwin Tree of Life project) and on the planet (Earth Biogenome Project) underway. To make sense of assembled genome data important features, such as protein-and non-coding genes, need to be identified and described; this general process is called annotation. Despite major advances in methods to automatically annotate genomes, the most accurate annotations require human assessment. However, the prohibitive cost usually prevents manual annotation (with curated updates) from being performed on individual species. A scalable alternative is to direct manual effort towards reference datasets and to harvest contributions from the broader research community. The resulting high-quality annotations can then be projected across species based on inferred homology. It is essential that the software used for annotation is fast, flexible and easy to use by different communities of annotators (professional curators, bench biologists, or curious non-experts). Of the currently available software platforms to annotate genomes, Artemis and Apollo are the two most popular and have been in wide use for 20 years. Artemis, developed at the Sanger Institute, has been used primarily for viewing, annotating and analysing the genomes of prokaryotic and eukaryotic microbes. A major strength of Artemis is its companion the ‘Artemis Comparison Tool' (ACT) that allows gene structures to be created or edited in the context of discovering and exploring genome conservation. A major limitation of both Artemis and ACT is that the software performs badly on sequences larger than a few tens of megabases. Like Artemis, Apollo started as a desktop tool, but was redesigned as a web-based tool and now runs on a shared server so that multiple users can browse and create annotations across the same genome simultaneously. Apollo comfortably handles any size genome and scales well with multiple concurrent users. This project will integrate the best of Artemis and Apollo to create a single higher performance annotation platform. The new Apollo will benefit from modern and modular architecture, for collaborative development and improved sustainability. Apollo will also be enhanced with new data interfaces, developed in collaboration with the EMBL-EBI group, so that genome comparison data can be accessed across servers, and annotation performed in the context of exploring synteny. The new generation of annotation tool will replace the existing Artemis and Apollo projects and be integrated into major genome annotation projects as well as retaining is usability by individual small-scale users.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.