zMAP toolset: model-based analysis of large-scale proteomic data via a variance stabilizing z-transformation

被引:0
|
作者
Gui, Xiuqi [1 ]
Huang, Jing [1 ]
Ruan, Linjie [2 ]
Wu, Yanjun [3 ]
Guo, Xuan [1 ]
Cao, Ruifang [1 ]
Zhou, Shuhan [1 ]
Tan, Fengxiang [1 ]
Zhu, Hongwen [4 ]
Li, Mushan [5 ]
Zhang, Guoqing [1 ]
Zhou, Hu [4 ]
Zhan, Lixing [3 ]
Liu, Xin [2 ]
Tu, Shiqi [1 ]
Shao, Zhen [1 ]
机构
[1] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Nutr & Hlth, CAS Key Lab Computat Biol, Shanghai 200031, Peoples R China
[2] Chinese Acad Sci, Univ Chinese Acad Sci, Key Lab Epigenet Regulat & Intervent, Shanghai Inst Biochem Cell & Biol,CAS Ctr Excellen, Shanghai 200031, Peoples R China
[3] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Nutr & Hlth, CAS Key Lab Nutr Metab & Food Safety, Shanghai 200031, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Mat Med, Analyt Res Ctr Organ & Biol Mol, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[5] Penn State Univ, Dept Stat, University Pk, PA 16802 USA
来源
GENOME BIOLOGY | 2024年 / 25卷 / 01期
基金
中国国家自然科学基金;
关键词
INTEGRATED PROTEOGENOMIC CHARACTERIZATION; RELATIVE QUANTIFICATION; MOLECULAR SIGNATURES; RATIO COMPRESSION; METABOLISM; CANCER; ITRAQ; QUANTITATION; INSIGHTS; REVEALS;
D O I
10.1186/s13059-024-03382-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Isobaric labeling-based mass spectrometry (ILMS) has been widely used to quantify, on a proteome-wide scale, the relative protein abundance in different biological conditions. However, large-scale ILMS data sets typically involve multiple runs of mass spectrometry, bringing great computational difficulty to the integration of ILMS samples. We present zMAP, a toolset that makes ILMS intensities comparable across mass spectrometry runs by modeling the associated mean-variance dependence and accordingly applying a variance stabilizing z-transformation. The practical utility of zMAP is demonstrated in several case studies involving the dynamics of cell differentiation and the heterogeneity across cancer patients.
引用
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页数:30
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