• 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

异质性疾病中微阵列的改良显著性分析

Modified Significance Analysis of Microarrays in Heterogeneous Diseases.

作者信息

Tzeng I-Shiang

机构信息

Department of Research, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei 231, Taiwan.

Department of Statistics, National Taipei University, Taipei 237, Taiwan.

出版信息

J Pers Med. 2021 Jan 20;11(2):62. doi: 10.3390/jpm11020062.

DOI:10.3390/jpm11020062
PMID:33498359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7909396/
Abstract

Significance analysis of microarrays (SAM) provides researchers with a non-parametric score for each gene based on repeated measurements. However, it may lose certain power in general statistical tests to correctly detect differentially expressed genes (DEGs) which violate homogeneity. Monte Carlo simulation shows that the "half SAM score" can maintain type I error rates of about 0.05 based on assumptions of normal and non-normal distributions. The author found 265 DEGs using the half SAM scoring, more than the 119 DEGs detected by SAM, with the false discovery rate controlled at 0.05. In conclusion, the author recommends the half SAM scoring method to detect DEGs in data that show heterogeneity.

摘要

微阵列显著性分析(SAM)基于重复测量为每个基因提供了一个非参数得分。然而,在一般统计检验中,它可能会在正确检测违反同质性的差异表达基因(DEG)方面失去一定的功效。蒙特卡罗模拟表明,基于正态和非正态分布的假设,“半SAM得分”可以维持约0.05的I型错误率。作者使用半SAM评分发现了265个DEG,比SAM检测到的119个DEG更多,且错误发现率控制在0.05。总之,作者推荐使用半SAM评分方法来检测显示异质性的数据中的DEG。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/2caa6fffaf58/jpm-11-00062-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/4316db476717/jpm-11-00062-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/18bc8fdef4fc/jpm-11-00062-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/f09213f80bba/jpm-11-00062-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/643f5e73f945/jpm-11-00062-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/2caa6fffaf58/jpm-11-00062-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/4316db476717/jpm-11-00062-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/18bc8fdef4fc/jpm-11-00062-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/f09213f80bba/jpm-11-00062-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/643f5e73f945/jpm-11-00062-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990a/7909396/2caa6fffaf58/jpm-11-00062-g005.jpg

相似文献

1
Modified Significance Analysis of Microarrays in Heterogeneous Diseases.异质性疾病中微阵列的改良显著性分析
J Pers Med. 2021 Jan 20;11(2):62. doi: 10.3390/jpm11020062.
2
Detecting differentially expressed genes by relative entropy.通过相对熵检测差异表达基因。
J Theor Biol. 2005 Jun 7;234(3):395-402. doi: 10.1016/j.jtbi.2004.11.039. Epub 2005 Jan 24.
3
A robust statistical procedure to discover expression biomarkers using microarray genomic expression data.一种利用微阵列基因组表达数据发现表达生物标志物的强大统计程序。
J Zhejiang Univ Sci B. 2006 Aug;7(8):603-7. doi: 10.1631/jzus.2006.B0603.
4
Detecting differentially expressed genes in heterogeneous diseases using control-only analysis of variance.使用仅对照方差分析检测异质疾病中的差异表达基因。
Ann Epidemiol. 2012 Aug;22(8):598-602. doi: 10.1016/j.annepidem.2012.04.017. Epub 2012 May 31.
5
Support vector machine quantile regression for detecting differentially expressed genes in microarray analysis.用于在微阵列分析中检测差异表达基因的支持向量机分位数回归
Methods Inf Med. 2008;47(5):459-67.
6
An investigation on performance of Significance Analysis of Microarray (SAM) for the comparisons of several treatments with one control in the presence of small-variance genes.在存在小方差基因的情况下,对微阵列显著性分析(SAM)用于几种处理与一个对照进行比较的性能研究。
Biom J. 2008 Oct;50(5):801-23. doi: 10.1002/bimj.200710467.
7
A rank-based algorithm of differential expression analysis for small cell line data with statistical control.基于秩的差异表达分析算法,用于具有统计控制的小细胞系数据。
Brief Bioinform. 2019 Mar 22;20(2):482-491. doi: 10.1093/bib/bbx135.
8
Normal uniform mixture differential gene expression detection for cDNA microarrays.用于cDNA微阵列的正常均匀混合物差异基因表达检测
BMC Bioinformatics. 2005 Jul 12;6:173. doi: 10.1186/1471-2105-6-173.
9
Ranking candidate genes of esophageal squamous cell carcinomas based on differentially expressed genes and the topological properties of the co-expression network.基于差异表达基因和共表达网络拓扑性质对食管鳞癌候选基因进行排名。
Eur J Med Res. 2014 Oct 29;19(1):52. doi: 10.1186/s40001-014-0052-x.
10
Type I interferon related genes are common genes on the early stage after vaccination by meta-analysis of microarray data.通过对微阵列数据的荟萃分析,I型干扰素相关基因是疫苗接种后早期的常见基因。
Hum Vaccin Immunother. 2015;11(3):739-45. doi: 10.1080/21645515.2015.1008884.

引用本文的文献

1
Identification of circulating miRNA as early diagnostic molecular markers in malignant glioblastoma base on decision tree joint scoring algorithm.基于决策树联合评分算法的循环 miRNA 作为恶性脑胶质瘤早期诊断分子标志物的鉴定。
J Cancer Res Clin Oncol. 2023 Dec;149(20):17823-17836. doi: 10.1007/s00432-023-05448-w. Epub 2023 Nov 9.
2
Inferencing Bulk Tumor and Single-Cell Multi-Omics Regulatory Networks for Discovery of Biomarkers and Therapeutic Targets.推断肿瘤组织和单细胞多组学调控网络,以发现生物标志物和治疗靶点。
Cells. 2022 Dec 26;12(1):101. doi: 10.3390/cells12010101.

本文引用的文献

1
RNA-seq assistant: machine learning based methods to identify more transcriptional regulated genes.RNA-seq 辅助工具:基于机器学习的方法,以鉴定更多受转录调控的基因。
BMC Genomics. 2018 Jul 20;19(1):546. doi: 10.1186/s12864-018-4932-2.
2
Differential analysis of RNA-seq incorporating quantification uncertainty.整合定量不确定性的 RNA-seq 差异分析。
Nat Methods. 2017 Jul;14(7):687-690. doi: 10.1038/nmeth.4324. Epub 2017 Jun 5.
3
limma powers differential expression analyses for RNA-sequencing and microarray studies.limma为RNA测序和微阵列研究提供差异表达分析的动力。
Nucleic Acids Res. 2015 Apr 20;43(7):e47. doi: 10.1093/nar/gkv007. Epub 2015 Jan 20.
4
Colorectal cancer heterogeneity and targeted therapy: a case for molecular disease subtypes.结直肠癌异质性与靶向治疗:以分子疾病亚型为例。
Cancer Res. 2015 Jan 15;75(2):245-9. doi: 10.1158/0008-5472.CAN-14-2240.
5
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.使用DESeq2对RNA测序数据的倍数变化和离散度进行适度估计。
Genome Biol. 2014;15(12):550. doi: 10.1186/s13059-014-0550-8.
6
RNA-Seq transcriptome profiling identifies CRISPLD2 as a glucocorticoid responsive gene that modulates cytokine function in airway smooth muscle cells.RNA测序转录组分析确定CRISPLD2为一种糖皮质激素反应基因,其可调节气道平滑肌细胞中的细胞因子功能。
PLoS One. 2014 Jun 13;9(6):e99625. doi: 10.1371/journal.pone.0099625. eCollection 2014.
7
voom: Precision weights unlock linear model analysis tools for RNA-seq read counts.voom:精确权重为RNA测序读数计数解锁线性模型分析工具。
Genome Biol. 2014 Feb 3;15(2):R29. doi: 10.1186/gb-2014-15-2-r29.
8
Differential analysis of gene regulation at transcript resolution with RNA-seq.基于 RNA-seq 的转录分辨率下基因调控的差异分析。
Nat Biotechnol. 2013 Jan;31(1):46-53. doi: 10.1038/nbt.2450. Epub 2012 Dec 9.
9
Detecting differentially expressed genes in heterogeneous diseases using control-only analysis of variance.使用仅对照方差分析检测异质疾病中的差异表达基因。
Ann Epidemiol. 2012 Aug;22(8):598-602. doi: 10.1016/j.annepidem.2012.04.017. Epub 2012 May 31.
10
Finding consistent patterns: a nonparametric approach for identifying differential expression in RNA-Seq data.发现一致模式:一种用于鉴定 RNA-Seq 数据中差异表达的非参数方法。
Stat Methods Med Res. 2013 Oct;22(5):519-36. doi: 10.1177/0962280211428386. Epub 2011 Nov 28.