HiFiBGC:在PacBio HiFi读取的元基因组中改进生物合成基因集群检测的整体方法
Amit Yadav1,2, Srikrishna Subramanian3,4
1CSIR-Institute of Microbial Technology (IMTECH), Sector 39-A, Chandigarh, 160036, India. amityadav@imtech.res.in.
BMC genomics
|November 16, 2024
概括
HiFiBGC从长期阅读的元基因组中识别出更多的微生物生物合成基因集群 (BGCs). 这种计算工作流通过增强BGC从复杂的基因组数据的恢复来改善自然产品的发现.
科学领域:
- 微生物学 微生物学
- 生物信息学是一种生物信息学.
- 基因组学就是基因组学.
背景情况:
- 微生物产生有价值的生物活性天然产品,其编码由生物合成基因集群 (BGCs).
- 从基因组和元基因组数据中识别高通量BGC对于发现天然产品至关重要.
- 短读测序技术难以组装完整的BGC,特别是来自复杂的元基因组.
研究的目的:
- 开发一种改进的计算方法,用于在长时间读取的元基因组数据中识别BGC.
- 为了利用PacBio HiFi测序的最新进展,提高BGC恢复.
- 为了克服从复杂的元基因组组装完整的BGCs的局限性.
主要方法:
- 开发了HiFiBGC,一个命令行工作流,利用来自三个HiFi定制的元基因组组件的组合.
- 嵌入的未映射读取包含碎片化的BGCs的分析.
- 将工作流应用于四个不同的HiFi元基因组数据集.
主要成果:
- 与单个装配器方法相比,HiFiBGC平均发现了78%更多的BGC.
- 整体组装方法使BGC回收率提高了25%.
- 包括未映射的读数进一步增强了碎片化的BGCs的识别.
结论:
- HiFiBGC是一种有效的计算工作流程,用于识别长时间读取的HiFi元基因组中的BGC.
- 工作流程显著改善了BGC的回收,有助于天然产品的发现.
- HiFiBGC是用Python实现的,并在GitHub上提供.
更多相关视频
08:03Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations
Published on: December 7, 2021
2.1K
09:06High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq
Published on: October 5, 2018
10.2K
相关概念视频
RNA-seq
9.8K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
9.8K
Genome Annotation and Assembly
18.8K
The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
18.8K
