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BSGatlas: a unified Bacillus subtilis genome and transcriptome annotation atlas with enhanced information access

机译:Bsgatlas:具有增强信息访问的统一的芽孢杆菌基因组和转录组注释图集

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A large part of our current understanding of gene regulation in Gram-positive bacteria is based on Bacillus subtilis , as it is one of the most well studied bacterial model systems. The rapid growth in data concerning its molecular and genomic biology is distributed across multiple annotation resources. Consequently, the interpretation of data from further B. subtilis experiments becomes increasingly challenging in both low- and large-scale analyses. Additionally, B. subtilis annotation of structured RNA and non-coding RNA (ncRNA), as well as the operon structure, is still lagging behind the annotation of the coding sequences. To address these challenges, we created the B. subtilis genome atlas, BSGatlas, which integrates and unifies multiple existing annotation resources. Compared to any of the individual resources, the BSGatlas contains twice as many ncRNAs, while improving the positional annotation for 70 % of the ncRNAs. Furthermore, we combined known transcription start and termination sites with lists of known co-transcribed gene sets to create a comprehensive transcript map. The combination with transcription start/termination site annotations resulted in 717 new sets of co-transcribed genes and 5335 untranslated regions (UTRs). In comparison to existing resources, the number of 5′ and 3′ UTRs increased nearly fivefold, and the number of internal UTRs doubled. The transcript map is organized in 2266 operons, which provides transcriptional annotation for 92 % of all genes in the genome compared to the at most 82 % by previous resources. We predicted an off-target-aware genome-wide library of CRISPR–Cas9 guide RNAs, which we also linked to polycistronic operons. We provide the BSGatlas in multiple forms: as a website (https://rth.dk/resources/bsgatlas/), an annotation hub for display in the UCSC genome browser, supplementary tables and standardized GFF3 format, which can be used in large scale -omics studies. By complementing existing resources, the BSGatlas supports analyses of the B. subtilis genome and its molecular biology with respect to not only non-coding genes but also genome-wide transcriptional relationships of all genes.
机译:我们目前对革氏菌细菌的基因调控的大部分基于枯草芽孢杆菌,因为它是最良好的学习细菌模型系统之一。关于其分子和基因组生物学的数据的快速增长分布在多个注释资源上。因此,从进一步的B.枯草芽孢杆菌实验的解释在低和大规模分析中,枯草芽孢杆菌实验变得越来越具有挑战性。另外,B.枯草芽孢杆菌注释结构化RNA和非编码RNA(NCRNA)以及操纵子结构仍然滞后于编码序列的注释后面。为了解决这些挑战,我们创建了B.枯草芽孢杆菌基因组Atlas,Bsgatlas,它集成并统一了多个现有的注释资源。与任何个人资源相比,BSGATLAS包含两倍的NCRNA,同时改善了70%的NCRNA的位置注释。此外,我们将已知的转录开始和终止位点与已知的共转录基因集列表组合以创建综合的转录图。转录开始/终止位点注释的组合导致717种新的共转录基因和5335个未翻译的地区(UTRS)。与现有资源相比,5'和3'UTR的数量增加了几乎五倍,内部UTR的数量加倍。转录物图在2266台操纵子中组织,其在以前资源最多82%的最多82%相比,基因组中所有基因的92%提供了转录注释。我们预测了一个脱靶感知的CRISPR-CAS9指南RNA的偏离目标感知基因组图书馆,我们也与电力调节器相关联。我们以多种形式提供BSGATLAS:作为网站(https://rth.dk/resources/bsgatlas/),用于在UCSC基因组浏览器中显示的注释集线器,补充表和标准化GFF3格式,可用于大型规模 - MOTICS研究。通过补充现有资源,BSGATLAS支持B.枯草芽孢杆菌基因组及其分子生物学的分析,不仅是非编码基因,还支持所有基因的基因组转录关系。

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