• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
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
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
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 @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

全基因组测序在菌株验证方面的挑战与机遇。

Challenges and opportunities for strain verification by whole-genome sequencing.

机构信息

Colorado State University, Colorado, USA.

Genevia Technologies, Helsinki, Finland.

出版信息

Sci Rep. 2020 Apr 3;10(1):5873. doi: 10.1038/s41598-020-62364-6.

DOI:10.1038/s41598-020-62364-6
PMID:32245992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7125075/
Abstract

Laboratory strains, cell lines, and other genetic materials change hands frequently in the life sciences. Despite evidence that such materials are subject to mix-ups, contamination, and accumulation of secondary mutations, verification of strains and samples is not an established part of many experimental workflows. With the plummeting cost of next generation technologies, it is conceivable that whole genome sequencing (WGS) could be applied to routine strain and sample verification in the future. To demonstrate the need for strain validation by WGS, we sequenced haploid yeast segregants derived from a popular commercial mutant collection and identified several unexpected mutations. We determined that available bioinformatics tools may be ill-suited for verification and highlight the importance of finishing reference genomes for commonly used laboratory strains.

摘要

实验室品系、细胞系和其他遗传材料在生命科学领域经常转手。尽管有证据表明这些材料容易发生混淆、污染和次要突变的积累,但对品系和样本的验证并不是许多实验工作流程的既定部分。随着下一代技术成本的急剧下降,可以想象全基因组测序(WGS)将来可能会应用于常规的品系和样本验证。为了证明通过 WGS 进行品系验证的必要性,我们对来自一个受欢迎的商业突变体库的单倍体酵母分离子进行了测序,并鉴定出了几个意想不到的突变。我们确定现有的生物信息学工具可能不适合验证,并强调完成常用实验室品系参考基因组的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3b/7125075/11c327c456ec/41598_2020_62364_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3b/7125075/aac109491206/41598_2020_62364_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3b/7125075/43a4cfdb7cb2/41598_2020_62364_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3b/7125075/11c327c456ec/41598_2020_62364_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3b/7125075/aac109491206/41598_2020_62364_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3b/7125075/43a4cfdb7cb2/41598_2020_62364_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac3b/7125075/11c327c456ec/41598_2020_62364_Fig3_HTML.jpg

相似文献

1
Challenges and opportunities for strain verification by whole-genome sequencing.全基因组测序在菌株验证方面的挑战与机遇。
Sci Rep. 2020 Apr 3;10(1):5873. doi: 10.1038/s41598-020-62364-6.
2
Assessment of inactivating stop codon mutations in forty Saccharomyces cerevisiae strains: implications for [PSI] prion- mediated phenotypes.评估四十株酿酒酵母菌株中的无义突变:对[PSI]朊病毒介导表型的影响。
PLoS One. 2011;6(12):e28684. doi: 10.1371/journal.pone.0028684. Epub 2011 Dec 15.
3
Validation of a Bioinformatics Workflow for Routine Analysis of Whole-Genome Sequencing Data and Related Challenges for Pathogen Typing in a European National Reference Center: as a Proof-of-Concept.用于全基因组测序数据常规分析的生物信息学工作流程的验证以及欧洲国家参考中心病原体分型的相关挑战:作为概念验证
Front Microbiol. 2019 Mar 6;10:362. doi: 10.3389/fmicb.2019.00362. eCollection 2019.
4
Validation strategy of a bioinformatics whole genome sequencing workflow for Shiga toxin-producing using a reference collection extensively characterized with conventional methods.基于经传统方法广泛特征分析的参考集,建立用于产志贺毒素的生物信息学全基因组测序工作流程的验证策略。
Microb Genom. 2021 Mar;7(3). doi: 10.1099/mgen.0.000531. Epub 2021 Mar 3.
5
Evaluation of Whole Genome Sequencing Data.全基因组测序数据评估
Methods Mol Biol. 2019;1956:321-336. doi: 10.1007/978-1-4939-9151-8_15.
6
Whole-Genome Sequencing of Yeast Cells.酵母细胞的全基因组测序
Curr Protoc Mol Biol. 2019 Sep;128(1):e103. doi: 10.1002/cpmb.103.
7
Adaptive Laboratory Evolution and Reverse Engineering of Single-Vitamin Prototrophies in Saccharomyces cerevisiae.在酿酒酵母中进行单维生素原养型的适应性实验室进化和反向工程。
Appl Environ Microbiol. 2020 Jun 2;86(12). doi: 10.1128/AEM.00388-20.
8
Whole-genome based strain identification of fowlpox virus directly from cutaneous tissue and propagated virus.从皮肤组织和增殖病毒中直接进行禽痘病毒的全基因组种系分析。
PLoS One. 2021 Dec 16;16(12):e0261122. doi: 10.1371/journal.pone.0261122. eCollection 2021.
9
Engineered yeast genomes accurately assembled from pure and mixed samples.工程酵母基因组可从纯样和混合样中准确组装。
Nat Commun. 2021 Mar 5;12(1):1485. doi: 10.1038/s41467-021-21656-9.
10
Genomes of the Mouse Collaborative Cross.小鼠协作杂交群体的基因组
Genetics. 2017 Jun;206(2):537-556. doi: 10.1534/genetics.116.198838.

引用本文的文献

1
Enhanced metagenomic strategies for elucidating the complexities of gut microbiota: a review.用于阐明肠道微生物群复杂性的增强宏基因组学策略:综述
Front Microbiol. 2025 Aug 26;16:1626002. doi: 10.3389/fmicb.2025.1626002. eCollection 2025.
2
Sequencing Strategy to Ensure Accurate Plasmid Assembly.确保准确质粒组装的测序策略。
ACS Synth Biol. 2024 Dec 20;13(12):4099-4109. doi: 10.1021/acssynbio.4c00539. Epub 2024 Nov 7.
3
Genetic Analysis and Fine Mapping of QTL for the Erect Leaf in Mutant Induced through Fast Neutron in Wheat.

本文引用的文献

1
Computational tools to unmask transposable elements.用于揭示转座元件的计算工具。
Nat Rev Genet. 2018 Nov;19(11):688-704. doi: 10.1038/s41576-018-0050-x.
2
Cyberbiosecurity: From Naive Trust to Risk Awareness.网络生物安保:从盲目信任到风险意识
Trends Biotechnol. 2018 Jan;36(1):4-7. doi: 10.1016/j.tibtech.2017.10.012. Epub 2017 Dec 7.
3
Reference standards for next-generation sequencing.下一代测序的参考标准。
小麦快中子诱变突变体直立叶QTL的遗传分析与精细定位
Biology (Basel). 2024 Jun 11;13(6):430. doi: 10.3390/biology13060430.
4
Discovery and characterization of a novel pathogen sp. nov. associated with pear dieback: taxonomic insights and genomic analysis.与梨树衰退相关的新型病原体sp. nov. 的发现与特征分析:分类学见解与基因组分析
Front Microbiol. 2024 May 9;15:1365685. doi: 10.3389/fmicb.2024.1365685. eCollection 2024.
5
Sequencing Strategy to Ensure Accurate Plasmid Assembly.确保准确质粒组装的测序策略。
bioRxiv. 2024 Jun 10:2024.03.25.586694. doi: 10.1101/2024.03.25.586694.
6
Identification of a common secondary mutation in the knockout collection conferring a cell fusion-defective phenotype.在敲除文库中鉴定出一种常见的赋予细胞融合缺陷表型的二次突变。
Microbiol Spectr. 2023 Aug 25;11(5):e0208723. doi: 10.1128/spectrum.02087-23.
7
and Negatively Interact during Oxidative Stress.并且在氧化应激期间产生负向相互作用。
Microorganisms. 2021 Dec 14;9(12):2584. doi: 10.3390/microorganisms9122584.
8
Genetic interactions derived from high-throughput phenotyping of 6589 yeast cell cycle mutants.通过对 6589 个酵母细胞周期突变体进行高通量表型分析得到的遗传相互作用。
NPJ Syst Biol Appl. 2020 May 6;6(1):11. doi: 10.1038/s41540-020-0134-z.
Nat Rev Genet. 2017 Aug;18(8):473-484. doi: 10.1038/nrg.2017.44. Epub 2017 Jun 19.
4
Detection of on-target and off-target mutations generated by CRISPR/Cas9 and other sequence-specific nucleases.CRISPR/Cas9 及其他序列特异性核酸酶产生的靶标和脱靶突变的检测。
Biotechnol Adv. 2017 Jan-Feb;35(1):95-104. doi: 10.1016/j.biotechadv.2016.12.003. Epub 2016 Dec 21.
5
Genetic variability in a frozen batch of MCF-7 cells invisible in routine authentication affecting cell function.MCF-7 细胞冻存批次中的遗传变异在常规鉴定中不可见,影响细胞功能。
Sci Rep. 2016 Jul 26;6:28994. doi: 10.1038/srep28994.
6
Standards for Cell Line Authentication and Beyond.细胞系鉴定及其他相关标准。
PLoS Biol. 2016 Jun 14;14(6):e1002476. doi: 10.1371/journal.pbio.1002476. eCollection 2016 Jun.
7
1,500 scientists lift the lid on reproducibility.1500名科学家揭开了可重复性的盖子。
Nature. 2016 May 26;533(7604):452-4. doi: 10.1038/533452a.
8
CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing.CNVkit:通过靶向DNA测序进行全基因组拷贝数检测与可视化
PLoS Comput Biol. 2016 Apr 21;12(4):e1004873. doi: 10.1371/journal.pcbi.1004873. eCollection 2016 Apr.
9
Whi5 phosphorylation embedded in the G1/S network dynamically controls critical cell size and cell fate.嵌入G1/S网络的Whi5磷酸化动态控制关键细胞大小和细胞命运。
Nat Commun. 2016 Apr 20;7:11372. doi: 10.1038/ncomms11372.
10
hybridSPAdes: an algorithm for hybrid assembly of short and long reads.hybridSPAdes:一种用于短读长和长读长混合组装的算法。
Bioinformatics. 2016 Apr 1;32(7):1009-15. doi: 10.1093/bioinformatics/btv688. Epub 2015 Nov 20.