HiFiBGC: an ensemble approach for improved biosynthetic gene cluster detection in PacBio HiFi-read metagenomes.

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2024-11-16 DOI:10.1186/s12864-024-10950-7
Amit Yadav, Srikrishna Subramanian
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引用次数: 0

Abstract

Background: Microbes produce diverse bioactive natural products with applications in fields such as medicine and agriculture. In their genomes, these natural products are encoded by physically clustered genes known as biosynthetic gene clusters (BGCs). Genome and metagenome sequencing advances have enabled high-throughput identification of BGCs as a promising avenue for natural product discovery. BGC mining from (meta)genomes using in silico tools has allowed access to a vast diversity of potentially novel natural products. However, a fundamental limitation has been the ability to assemble complete BGCs, especially from complex metagenomes. With their fragmented assemblies, short-read technologies struggle to recover complete BGCs, such as the long and repetitive nonribosomal peptide synthetase (NRPS) and polyketide synthase (PKS). Recent advances in long-read sequencing, such as the High Fidelity (HiFi) technology from PacBio, have reduced this limitation and can help retrieve both accurate and complete BGCs from metagenomes, warranting improvement in the existing BGC identification approach for better utilization of HiFi data.

Results: Here, we present HiFiBGC, a command-line-based workflow to identify BGCs in PacBio HiFi metagenomes. HiFiBGC leverages an ensemble of assemblies from three HiFi-tailored metagenome assemblers and the reads not represented in these assemblies. Based on our analyses of four HiFi metagenomic datasets from four different environments, we show that HiFiBGC identifies, on average, 78% more BGCs than the top-performing single-assembler-based method. This increase is due to HiFiBGC's ensemble assembly approach, which improves recovery by 25%, as well as from the inclusion of mostly fragmented BGCs identified in the unmapped reads.

Conclusions: HiFiBGC is a computational workflow for identifying BGCs in long-read HiFi metagenomes, implemented majorly using Python programming language and workflow manager Snakemake. HiFiBGC is available on GitHub at https://github.com/ay-amityadav/HiFiBGC under the MIT license. The code related to the figures and analyses presented in the manuscript is available at https://github.com/ay-amityadav/HiFiBGC_analyses .

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HiFiBGC:在 PacBio HiFi-read元基因组中改进生物合成基因簇检测的集合方法。
背景:微生物能产生多种具有生物活性的天然产物,可应用于医药和农业等领域。在它们的基因组中,这些天然产物由被称为生物合成基因簇(BGCs)的物理聚类基因编码。基因组和元基因组测序技术的进步使得高通量鉴定 BGCs 成为发现天然产品的一个很有前景的途径。利用硅学工具从(元)基因组中挖掘 BGC,可以获得种类繁多的潜在新型天然产物。然而,一个根本性的限制因素是组装完整 BGC 的能力,尤其是从复杂的元基因组中组装 BGC 的能力。短线程技术的组装比较零散,难以恢复完整的 BGCs,如长且重复的非核糖体肽合成酶(NRPS)和多酮肽合成酶(PKS)。长读数测序技术(如 PacBio 的高保真(HiFi)技术)的最新进展减少了这一限制,有助于从元基因组中检索到准确而完整的 BGC,因此有必要改进现有的 BGC 鉴定方法,以便更好地利用 HiFi 数据:结果:在此,我们介绍了 HiFiBGC,这是一种基于命令行的工作流程,用于识别 PacBio HiFi 元基因组中的 BGC。HiFiBGC利用了来自三个HiFi定制元基因组组装器的组装集合以及这些组装器中未体现的读数。根据我们对来自四种不同环境的四个 HiFi 元基因组数据集的分析,我们发现 HiFiBGC 识别的 BGC 平均比性能最高的基于单一组装器的方法多 78%。这一增长归功于 HiFiBGC 的集合组装方法,该方法将恢复率提高了 25%,同时也归功于纳入了未映射读数中识别出的大部分片段 BGC:HiFiBGC是一种在长读数HiFi元基因组中识别BGC的计算工作流,主要使用Python编程语言和工作流管理器Snakemake实现。HiFiBGC 可在 GitHub https://github.com/ay-amityadav/HiFiBGC 上以 MIT 许可发布。与手稿中的图表和分析相关的代码可在 https://github.com/ay-amityadav/HiFiBGC_analyses 上获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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