• 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

SCADIE:基于 SCAD 的迭代估计过程同时估计细胞类型比例和细胞类型特异性基因表达。

SCADIE: simultaneous estimation of cell type proportions and cell type-specific gene expressions using SCAD-based iterative estimating procedure.

机构信息

Department of Biostatistics, Yale School of Public Health, 60 College Street, New Haven, USA.

Department of Statistics, Sungkyunkwan University, 25-2, Sungkyunkwan-ro, Jongno-gu, Seoul, South Korea.

出版信息

Genome Biol. 2022 Jun 15;23(1):129. doi: 10.1186/s13059-022-02688-w.

DOI:10.1186/s13059-022-02688-w
PMID:35706040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9199219/
Abstract

A challenge in bulk gene differential expression analysis is to differentiate changes due to cell type-specific gene expression and cell type proportions. SCADIE is an iterative algorithm that simultaneously estimates cell type-specific gene expression profiles and cell type proportions, and performs cell type-specific differential expression analysis at the group level. Through its unique penalty and objective function, SCADIE more accurately identifies cell type-specific differentially expressed genes than existing methods, including those that may be missed from single cell RNA-Seq data. SCADIE has robust performance with respect to the choice of deconvolution methods and the sources and quality of input data.

摘要

批量基因差异表达分析面临的一个挑战是区分细胞类型特异性基因表达和细胞类型比例引起的变化。SCADIE 是一种迭代算法,可同时估计细胞类型特异性基因表达谱和细胞类型比例,并在组水平上进行细胞类型特异性差异表达分析。通过其独特的惩罚和目标函数,SCADIE 比现有的方法更准确地识别细胞类型特异性差异表达基因,包括那些可能从单细胞 RNA-Seq 数据中遗漏的基因。SCADIE 对于去卷积方法的选择以及输入数据的来源和质量具有稳健的性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/15885a4a4764/13059_2022_2688_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/201f89c6cee9/13059_2022_2688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/62f9d8596d45/13059_2022_2688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/f286acfbdcbc/13059_2022_2688_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/b24ecb209722/13059_2022_2688_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/4977ae9c44fd/13059_2022_2688_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/375448f5b62b/13059_2022_2688_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/a586aabc61b9/13059_2022_2688_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/15885a4a4764/13059_2022_2688_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/201f89c6cee9/13059_2022_2688_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/62f9d8596d45/13059_2022_2688_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/f286acfbdcbc/13059_2022_2688_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/b24ecb209722/13059_2022_2688_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/4977ae9c44fd/13059_2022_2688_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/375448f5b62b/13059_2022_2688_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/a586aabc61b9/13059_2022_2688_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdf6/9199219/15885a4a4764/13059_2022_2688_Fig8_HTML.jpg

相似文献

1
SCADIE: simultaneous estimation of cell type proportions and cell type-specific gene expressions using SCAD-based iterative estimating procedure.SCADIE:基于 SCAD 的迭代估计过程同时估计细胞类型比例和细胞类型特异性基因表达。
Genome Biol. 2022 Jun 15;23(1):129. doi: 10.1186/s13059-022-02688-w.
2
MuSiC2: cell-type deconvolution for multi-condition bulk RNA-seq data.MuSiC2:用于多条件批量 RNA-seq 数据的细胞类型去卷积。
Brief Bioinform. 2022 Nov 19;23(6). doi: 10.1093/bib/bbac430.
3
Deconvolution from bulk gene expression by leveraging sample-wise and gene-wise similarities and single-cell RNA-Seq data.通过利用样本和基因之间的相似性以及单细胞 RNA-Seq 数据进行批量基因表达的反卷积。
BMC Genomics. 2024 Sep 18;25(1):875. doi: 10.1186/s12864-024-10728-x.
4
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.
5
Omnibus and robust deconvolution scheme for bulk RNA sequencing data integrating multiple single-cell reference sets and prior biological knowledge.用于批量 RNA 测序数据的整体且稳健的去卷积方案,该方案整合了多个单细胞参考集和先验生物学知识。
Bioinformatics. 2022 Sep 30;38(19):4530-4536. doi: 10.1093/bioinformatics/btac563.
6
Iterative point set registration for aligning scRNA-seq data.迭代点集配准算法用于对齐 scRNA-seq 数据。
PLoS Comput Biol. 2020 Oct 27;16(10):e1007939. doi: 10.1371/journal.pcbi.1007939. eCollection 2020 Oct.
7
scAnno: a deconvolution strategy-based automatic cell type annotation tool for single-cell RNA-sequencing data sets.scAnno:一种基于去卷积策略的单细胞 RNA 测序数据集自动细胞类型注释工具。
Brief Bioinform. 2023 May 19;24(3). doi: 10.1093/bib/bbad179.
8
A component overlapping attribute clustering (COAC) algorithm for single-cell RNA sequencing data analysis and potential pathobiological implications.单细胞 RNA 测序数据分析的一种成分重叠属性聚类(COAC)算法及其潜在的病理生物学意义。
PLoS Comput Biol. 2019 Feb 19;15(2):e1006772. doi: 10.1371/journal.pcbi.1006772. eCollection 2019 Feb.
9
Assessing transcriptomic heterogeneity of single-cell RNASeq data by bulk-level gene expression data.通过批量水平基因表达数据评估单细胞RNA测序数据的转录组异质性。
BMC Bioinformatics. 2024 Jun 12;25(1):209. doi: 10.1186/s12859-024-05825-3.
10
LRcell: detecting the source of differential expression at the sub-cell-type level from bulk RNA-seq data.LRcell:从批量 RNA-seq 数据中检测亚细胞类型水平差异表达的来源。
Brief Bioinform. 2022 May 13;23(3). doi: 10.1093/bib/bbac063.

引用本文的文献

1
Statistical Inference of Cell-type Proportions Estimated from Bulk Expression Data.从批量表达数据估计细胞类型比例的统计推断
J Am Stat Assoc. 2024;119(548):2521-2532. doi: 10.1080/01621459.2024.2382435. Epub 2024 Sep 20.
2
Low-rank regression models for multiple binary responses and their applications to cancer cell-line encyclopedia data.用于多个二元响应的低秩回归模型及其在癌细胞系百科全书数据中的应用。
J Am Stat Assoc. 2024;119(545):202-216. doi: 10.1080/01621459.2022.2105704. Epub 2022 Sep 20.
3
BEDwARS: a robust Bayesian approach to bulk gene expression deconvolution with noisy reference signatures.

本文引用的文献

1
Cell type-aware analysis of RNA-seq data.RNA测序数据的细胞类型感知分析。
Nat Comput Sci. 2021 Apr;1(4):253-261. doi: 10.1038/s43588-021-00055-6. Epub 2021 Apr 15.
2
A computational method for direct imputation of cell type-specific expression profiles and cellular compositions from bulk-tissue RNA-Seq in brain disorders.一种用于从脑部疾病的大块组织RNA测序中直接推算细胞类型特异性表达谱和细胞组成的计算方法。
NAR Genom Bioinform. 2021 Jun 22;3(2):lqab056. doi: 10.1093/nargab/lqab056. eCollection 2021 Jun.
3
Single-cell RNA-seq reveals ectopic and aberrant lung-resident cell populations in idiopathic pulmonary fibrosis.
BEDwARS:一种具有稳健性的贝叶斯方法,可用于对具有噪声参考特征的批量基因表达解卷积。
Genome Biol. 2023 Aug 3;24(1):178. doi: 10.1186/s13059-023-03007-7.
4
A novel Bayesian framework for harmonizing information across tissues and studies to increase cell type deconvolution accuracy.一种新颖的贝叶斯框架,用于协调跨组织和研究的信息,以提高细胞类型去卷积的准确性。
Brief Bioinform. 2023 Jan 19;24(1). doi: 10.1093/bib/bbac616.
单细胞 RNA 测序揭示特发性肺纤维化中异位和异常的肺驻留细胞群体。
Sci Adv. 2020 Jul 8;6(28):eaba1983. doi: 10.1126/sciadv.aba1983. eCollection 2020 Jul.
4
Deconvolving the contributions of cell-type heterogeneity on cortical gene expression.解析细胞类型异质性对皮质基因表达的贡献。
PLoS Comput Biol. 2020 Aug 17;16(8):e1008120. doi: 10.1371/journal.pcbi.1008120. eCollection 2020 Aug.
5
SCDC: bulk gene expression deconvolution by multiple single-cell RNA sequencing references.SCDC:通过多个单细胞 RNA 测序参考进行批量基因表达去卷积。
Brief Bioinform. 2021 Jan 18;22(1):416-427. doi: 10.1093/bib/bbz166.
6
CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data.CDSeq:一种使用基因表达数据对异质样本进行全面剖析的全新去卷积方法。
PLoS Comput Biol. 2019 Dec 2;15(12):e1007510. doi: 10.1371/journal.pcbi.1007510. eCollection 2019 Dec.
7
NITUMID: Nonnegative matrix factorization-based Immune-TUmor MIcroenvironment Deconvolution.NITUMID:基于非负矩阵分解的免疫-肿瘤微环境分解。
Bioinformatics. 2020 Mar 1;36(5):1344-1350. doi: 10.1093/bioinformatics/btz748.
8
Screening of key genes associated with R‑CHOP immunochemotherapy and construction of a prognostic risk model in diffuse large B‑cell lymphoma.筛选与 R-CHOP 免疫化疗相关的关键基因,并构建弥漫性大 B 细胞淋巴瘤的预后风险模型。
Mol Med Rep. 2019 Oct;20(4):3679-3690. doi: 10.3892/mmr.2019.10627. Epub 2019 Aug 29.
9
Accurate estimation of cell-type composition from gene expression data.从基因表达数据中准确估计细胞类型组成。
Nat Commun. 2019 Jul 5;10(1):2975. doi: 10.1038/s41467-019-10802-z.
10
Comprehensive Integration of Single-Cell Data.单细胞数据的综合整合。
Cell. 2019 Jun 13;177(7):1888-1902.e21. doi: 10.1016/j.cell.2019.05.031. Epub 2019 Jun 6.