• 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

多物种 RNA-seq 差异表达分析的最佳实践。

Best practices on the differential expression analysis of multi-species RNA-seq.

机构信息

Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.

Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.

出版信息

Genome Biol. 2021 Apr 29;22(1):121. doi: 10.1186/s13059-021-02337-8.

DOI:10.1186/s13059-021-02337-8
PMID:33926528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8082843/
Abstract

Advances in transcriptome sequencing allow for simultaneous interrogation of differentially expressed genes from multiple species originating from a single RNA sample, termed dual or multi-species transcriptomics. Compared to single-species differential expression analysis, the design of multi-species differential expression experiments must account for the relative abundances of each organism of interest within the sample, often requiring enrichment methods and yielding differences in total read counts across samples. The analysis of multi-species transcriptomics datasets requires modifications to the alignment, quantification, and downstream analysis steps compared to the single-species analysis pipelines. We describe best practices for multi-species transcriptomics and differential gene expression.

摘要

转录组测序技术的进步使得能够从单个 RNA 样本中同时检测来自多个物种的差异表达基因,这种方法被称为双物种或多物种转录组学。与单物种差异表达分析相比,多物种差异表达实验的设计必须考虑到样本中每个感兴趣的生物体的相对丰度,通常需要富集方法,并导致样本之间的总读计数存在差异。与单物种分析流程相比,多物种转录组数据集的分析需要对比对、定量和下游分析步骤进行修改。我们描述了多物种转录组学和差异基因表达的最佳实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/130c13d54242/13059_2021_2337_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/f22819257dd2/13059_2021_2337_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/0dd58c6d4445/13059_2021_2337_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/ee98310b1486/13059_2021_2337_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/130c13d54242/13059_2021_2337_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/f22819257dd2/13059_2021_2337_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/0dd58c6d4445/13059_2021_2337_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/ee98310b1486/13059_2021_2337_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a354/8082843/130c13d54242/13059_2021_2337_Fig4_HTML.jpg

相似文献

1
Best practices on the differential expression analysis of multi-species RNA-seq.多物种 RNA-seq 差异表达分析的最佳实践。
Genome Biol. 2021 Apr 29;22(1):121. doi: 10.1186/s13059-021-02337-8.
2
Normalization of Single-Cell RNA-Seq Data.单细胞 RNA-Seq 数据的归一化处理。
Methods Mol Biol. 2021;2284:303-329. doi: 10.1007/978-1-0716-1307-8_17.
3
Using RNentropy to Detect Significant Variation in Gene Expression Across Multiple RNA-Seq or Single-Cell RNA-Seq Samples.使用 RNentropy 检测多个 RNA-Seq 或单细胞 RNA-Seq 样本中基因表达的显著变化。
Methods Mol Biol. 2021;2284:77-96. doi: 10.1007/978-1-0716-1307-8_6.
4
Short-Read RNA-Seq.短读 RNA 测序。
Methods Mol Biol. 2024;2822:245-262. doi: 10.1007/978-1-0716-3918-4_17.
5
Comparative Methods for Demystifying Spatial Transcriptomics.比较方法解析空间转录组学
Methods Mol Biol. 2024;2802:515-546. doi: 10.1007/978-1-0716-3838-5_17.
6
Nanopore RNA Sequencing Analysis.纳米孔 RNA 测序分析。
Methods Mol Biol. 2021;2284:569-578. doi: 10.1007/978-1-0716-1307-8_31.
7
Live-seq enables temporal transcriptomic recording of single cells.活细胞测序能够对单细胞进行时间转录组记录。
Nature. 2022 Aug;608(7924):733-740. doi: 10.1038/s41586-022-05046-9. Epub 2022 Aug 17.
8
Single-Cell Capture, RNA-seq, and Transcriptome Analysis from the Neural Retina.来自神经视网膜的单细胞捕获、RNA测序及转录组分析。
Methods Mol Biol. 2020;2092:159-186. doi: 10.1007/978-1-0716-0175-4_12.
9
A Comprehensive Survey of Statistical Approaches for Differential Expression Analysis in Single-Cell RNA Sequencing Studies.单细胞 RNA 测序研究中差异表达分析的统计方法综合综述。
Genes (Basel). 2021 Dec 2;12(12):1947. doi: 10.3390/genes12121947.
10
Current and Future Methods for mRNA Analysis: A Drive Toward Single Molecule Sequencing.mRNA分析的当前及未来方法:迈向单分子测序的动力
Methods Mol Biol. 2018;1783:209-241. doi: 10.1007/978-1-4939-7834-2_11.

引用本文的文献

1
A Scorecard for Information Synthesis in Multiple Experimental Conditions: Application to Bacterial Biofilm Matrix Transcriptomics.多实验条件下信息综合的记分卡:应用于细菌生物膜基质转录组学
Curr Microbiol. 2025 Sep 9;82(10):497. doi: 10.1007/s00284-025-04435-3.
2
Core Perturbomes of and Using a Machine Learning Approach.使用机器学习方法的[具体研究对象1]和[具体研究对象2]的核心扰动组。 (你原文中“of and ”表述不完整,这里是根据常见情况补充后翻译的,你可根据实际调整。)
Pathogens. 2025 Aug 7;14(8):788. doi: 10.3390/pathogens14080788.
3
Phillyrin prevents calcium oxalate kidney stones through the PPARγ signaling pathway.

本文引用的文献

1
FADU: a Quantification Tool for Prokaryotic Transcriptomic Analyses.FADU:一种用于原核生物转录组分析的定量工具。
mSystems. 2021 Jan 12;6(1):e00917-20. doi: 10.1128/mSystems.00917-20.
2
Microbial single-cell RNA sequencing by split-pool barcoding.基于拆分池条形码的微生物单细胞 RNA 测序。
Science. 2021 Feb 19;371(6531). doi: 10.1126/science.aba5257. Epub 2020 Dec 17.
3
Alignment and mapping methodology influence transcript abundance estimation.比对和映射方法会影响转录本丰度的估计。
连翘苷通过PPARγ信号通路预防草酸钙肾结石。
Ren Fail. 2025 Dec;47(1):2486559. doi: 10.1080/0886022X.2025.2486559. Epub 2025 Aug 18.
4
Multi-omics insights of immune cells in the risk and prognosis of idiopathic membranous nephropathy.免疫细胞在特发性膜性肾病风险和预后中的多组学见解
Commun Biol. 2025 Aug 10;8(1):1192. doi: 10.1038/s42003-025-08642-3.
5
Cluefish: mining the dark matter of transcriptional data series with over-representation analysis enhanced by aggregated biological prior knowledge.线索鱼:利用聚合生物学先验知识增强的过度表达分析挖掘转录数据系列的暗物质。
NAR Genom Bioinform. 2025 Jul 30;7(3):lqaf103. doi: 10.1093/nargab/lqaf103. eCollection 2025 Sep.
6
"Misuse" of RNA-seq data in microbiome studies: A cautionary tale of poly(A).微生物组研究中RNA测序数据的“误用”:一个关于聚腺苷酸(poly(A))的警示故事
mLife. 2025 Jun 2;4(3):227-231. doi: 10.1002/mlf2.70012. eCollection 2025 Jun.
7
Evaluating the Effectiveness of Various Small RNA Alignment Techniques in Transcriptomic Analysis by Examining Different Sources of Variability Through a Multi-Alignment Approach.通过多比对方法检查不同变异来源,评估各种小RNA比对技术在转录组分析中的有效性。
Methods Protoc. 2025 Jun 17;8(3):65. doi: 10.3390/mps8030065.
8
Comparative Transcriptome Reveals Conserved Gene Expression in Reproductive Organs in Solanaceae.比较转录组揭示茄科生殖器官中保守的基因表达
Int J Mol Sci. 2025 Apr 10;26(8):3568. doi: 10.3390/ijms26083568.
9
Significance of KLK7 expression, polymorphisms, and function in sheep horn growth.KLK7在绵羊角生长中的表达、多态性及功能的意义
BMC Genomics. 2025 Jan 27;26(1):78. doi: 10.1186/s12864-024-11130-3.
10
Dysregulation of mRNA expression by hsa-miR-186 overexpression in arsenic-induced skin carcinogenesis.在砷诱导的皮肤癌发生过程中,hsa-miR-186过表达导致mRNA表达失调。
Toxicol Appl Pharmacol. 2025 Feb;495:117209. doi: 10.1016/j.taap.2024.117209. Epub 2024 Dec 22.
Genome Biol. 2020 Sep 7;21(1):239. doi: 10.1186/s13059-020-02151-8.
4
Modeling the metabolic interplay between a parasitic worm and its bacterial endosymbiont allows the identification of novel drug targets.对寄生虫与其内共生细菌之间代谢相互作用的建模,有助于鉴定新的药物靶点。
Elife. 2020 Aug 11;9:e51850. doi: 10.7554/eLife.51850.
5
A Meta-Analysis of Transcriptomics Reveals a Stage-Specific Transcriptional Response Shared Across Different Hosts.一项转录组学的荟萃分析揭示了不同宿主间共有的阶段特异性转录反应。
G3 (Bethesda). 2020 Sep 2;10(9):3243-3260. doi: 10.1534/g3.120.401534.
6
Evaluation of methods for detecting human reads in microbial sequencing datasets.评估微生物测序数据集检测人读的方法。
Microb Genom. 2020 Jul;6(7). doi: 10.1099/mgen.0.000393.
7
Prokaryotic single-cell RNA sequencing by in situ combinatorial indexing.基于原位组合索引的原核单细胞 RNA 测序。
Nat Microbiol. 2020 Oct;5(10):1192-1201. doi: 10.1038/s41564-020-0729-6. Epub 2020 May 25.
8
ORF Capture-Seq as a versatile method for targeted identification of full-length isoforms.ORF 捕获测序是一种用于靶向鉴定全长异构体的通用方法。
Nat Commun. 2020 May 11;11(1):2326. doi: 10.1038/s41467-020-16174-z.
9
Evaluating the genome and resistome of extensively drug-resistant Klebsiella pneumoniae using native DNA and RNA Nanopore sequencing.利用天然 DNA 和 RNA 纳米孔测序技术评估广泛耐药肺炎克雷伯菌的基因组和耐药组。
Gigascience. 2020 Feb 1;9(2). doi: 10.1093/gigascience/giaa002.
10
Dual RNA-Seq of Mtb-Infected Macrophages In Vivo Reveals Ontologically Distinct Host-Pathogen Interactions.体内感染巨噬细胞的结核分枝杆菌的 Dual RNA-Seq 揭示了具有不同本体论特征的宿主-病原体相互作用。
Cell Rep. 2020 Jan 14;30(2):335-350.e4. doi: 10.1016/j.celrep.2019.12.033.