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A Normalization-Free and Nonparametric Method Sharpens Large-Scale Transcriptome Analysis and Reveals Common Gene Alteration Patterns in Cancers.


ABSTRACT: Heterogeneity in transcriptional data hampers the identification of differentially expressed genes (DEGs) and understanding of cancer, essentially because current methods rely on cross-sample normalization and/or distribution assumption-both sensitive to heterogeneous values. Here, we developed a new method, Cross-Value Association Analysis (CVAA), which overcomes the limitation and is more robust to heterogeneous data than the other methods. Applying CVAA to a more complex pan-cancer dataset containing 5,540 transcriptomes discovered numerous new DEGs and many previously rarely explored pathways/processes; some of them were validated, both in vitro and in vivo, to be crucial in tumorigenesis, e.g., alcohol metabolism (ADH1B), chromosome remodeling (NCAPH) and complement system (Adipsin). Together, we present a sharper tool to navigate large-scale expression data and gain new mechanistic insights into tumorigenesis.

SUBMITTER: Li QG 

PROVIDER: S-EPMC5562223 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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A Normalization-Free and Nonparametric Method Sharpens Large-Scale Transcriptome Analysis and Reveals Common Gene Alteration Patterns in Cancers.

Li Qi-Gang QG   He Yong-Han YH   Wu Huan H   Yang Cui-Ping CP   Pu Shao-Yan SY   Fan Song-Qing SQ   Jiang Li-Ping LP   Shen Qiu-Shuo QS   Wang Xiao-Xiong XX   Chen Xiao-Qiong XQ   Yu Qin Q   Li Ying Y   Sun Chang C   Wang Xiangting X   Zhou Jumin J   Li Hai-Peng HP   Chen Yong-Bin YB   Kong Qing-Peng QP  

Theranostics 20170708 11


Heterogeneity in transcriptional data hampers the identification of differentially expressed genes (DEGs) and understanding of cancer, essentially because current methods rely on cross-sample normalization and/or distribution assumption-both sensitive to heterogeneous values. Here, we developed a new method, Cross-Value Association Analysis (CVAA), which overcomes the limitation and is more robust to heterogeneous data than the other methods. Applying CVAA to a more complex pan-cancer dataset co  ...[more]

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