文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

细菌泛基因组分析方法的陷阱:以结核分枝杆菌和另外两种克隆性较低的细菌物种为例的研究

Pitfalls of bacterial pan-genome analysis approaches: a case study of Mycobacterium tuberculosis and two less clonal bacterial species.

作者信息

Marin Maximillian G, Quinones-Olvera Natalia, Wippel Christoph, Behruznia Mahboobeh, Jeffrey Brendan M, Harris Michael, Mann Brendon C, Rosenthal Alex, Jacobson Karen R, Warren Robin M, Li Heng, Meehan Conor J, Farhat Maha R

机构信息

Department of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, United States.

Department of Biosciences, Nottingham Trent University, Nottingham, NG1 4FQ, United Kingdom.

出版信息

Bioinformatics. 2025 May 6;41(5). doi: 10.1093/bioinformatics/btaf219.


DOI:10.1093/bioinformatics/btaf219
PMID:40341387
Abstract

SUMMARY: Pan-genome analysis is a fundamental tool for studying bacterial genome evolution; however, the variety in methods used to define and measure the pan-genome poses challenges to the interpretation and reliability of results. Using Mycobacterium tuberculosis, a clonally evolving bacterium with a small accessory genome, as a model system, we systematically evaluated sources of variability in pan-genome estimates. Our analysis revealed that differences in assembly type (short-read versus hybrid), annotation pipeline, and pan-genome software, significantly impact predictions of core and accessory genome size. Extending our analysis to two additional bacterial species, Escherichia coli and Staphylococcus aureus, we observed consistent tool-dependent biases but species-specific patterns in pan-genome variability. Our findings highlight the importance of integrating nucleotide- and protein-level analyses to improve the reliability and reproducibility of pan-genome studies across diverse bacterial populations. AVAILABILITY AND IMPLEMENTATION: Panqc is freely available under an MIT license at https://github.com/maxgmarin/panqc.

摘要

摘要:泛基因组分析是研究细菌基因组进化的基本工具;然而,用于定义和测量泛基因组的方法多种多样,这给结果的解释和可靠性带来了挑战。我们以结核分枝杆菌(一种具有小的辅助基因组的克隆进化细菌)作为模型系统,系统地评估了泛基因组估计中变异性的来源。我们的分析表明,组装类型(短读长与混合组装)、注释流程和泛基因组软件的差异,会显著影响核心基因组和辅助基因组大小的预测。将我们的分析扩展到另外两种细菌物种,大肠杆菌和金黄色葡萄球菌,我们观察到了一致的工具依赖性偏差,但泛基因组变异性存在物种特异性模式。我们的研究结果强调了整合核苷酸水平和蛋白质水平分析对于提高跨不同细菌群体的泛基因组研究的可靠性和可重复性的重要性。 可用性和实现方式:Panqc在https://github.com/maxgmarin/panqc上根据MIT许可免费提供。

相似文献

[1]
Pitfalls of bacterial pan-genome analysis approaches: a case study of Mycobacterium tuberculosis and two less clonal bacterial species.

Bioinformatics. 2025-5-6

[2]
Comparative Genomics of Borderline Oxacillin-Resistant Staphylococcus aureus Detected during a Pseudo-outbreak of Methicillin-Resistant S. aureus in a Neonatal Intensive Care Unit.

mBio. 2022-2-22

[3]
Prescription of Controlled Substances: Benefits and Risks

2025-1

[4]
Whole-genome phenotype prediction with machine learning: open problems in bacterial genomics.

Bioinformatics. 2025-7-1

[5]
SAKit: An all-in-one analysis pipeline for identifying novel proteins resulting from variant events at both large and small scales.

J Bioinform Comput Biol. 2024-10

[6]
Xpert MTB/RIF assay for extrapulmonary tuberculosis and rifampicin resistance.

Cochrane Database Syst Rev. 2018-8-27

[7]
Xpert® MTB/RIF assay for pulmonary tuberculosis and rifampicin resistance in adults.

Cochrane Database Syst Rev. 2013-1-31

[8]
A new method for detecting mixed Mycobacterium tuberculosis infection and reconstructing constituent strains provides insights into transmission.

Genome Med. 2025-1-27

[9]
Lessons learned: overcoming common challenges in reconstructing the SARS-CoV-2 genome from short-read sequencing data via CoVpipe2.

F1000Res. 2024-4-16

[10]
Xpert MTB/XDR for detection of pulmonary tuberculosis and resistance to isoniazid, fluoroquinolones, ethionamide, and amikacin.

Cochrane Database Syst Rev. 2022-5-18

引用本文的文献

[1]
Linkage-based ortholog refinement in bacterial pangenomes with CLARC.

Nucleic Acids Res. 2025-6-20

[2]
Sequence Modeling Is Not Evolutionary Reasoning.

bioRxiv. 2025-6-27

本文引用的文献

[1]
Exploring gene content with pangene graphs.

Bioinformatics. 2024-7-23

[2]
Evolution and emergence of Mycobacterium tuberculosis.

FEMS Microbiol Rev. 2024-3-1

[3]
Diversification of gene content in the complex is determined by phylogenetic and ecological signatures.

Microbiol Spectr. 2024-2-6

[4]
The intra-host evolutionary landscape and pathoadaptation of persistent in chronic rhinosinusitis.

Microb Genom. 2023-11

[5]
Challenges in prokaryote pangenomics.

Microb Genom. 2023-5

[6]
Robust analysis of prokaryotic pangenome gene gain and loss rates with Panstripe.

Genome Res. 2023-1

[7]
Protein-to-genome alignment with miniprot.

Bioinformatics. 2023-1-1

[8]
Evaluation of Nanopore sequencing for Mycobacterium tuberculosis drug susceptibility testing and outbreak investigation: a genomic analysis.

Lancet Microbe. 2023-2

[9]
Multiclonal human origin and global expansion of an endemic bacterial pathogen of livestock.

Proc Natl Acad Sci U S A. 2022-12-13

[10]
The rate and role of pseudogenes of the complex.

Microb Genom. 2022-10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索