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Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies

With the increasing availability and dropping cost of high-throughput technology in recent years, many-omics datasets have accumulated in the public domain. Combining multiple transcriptomic studies on related hypothesis via meta-analysis can improve statistical power and reproducibility over single...

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Autores principales: Ye, Zhenyao, Ke, Hongjie, Chen, Shuo, Cruz-Cano, Raul, He, Xin, Zhang, Jing, Dorgan, Joanne, Milton, Donald K., Ma, Tianzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8283696/
https://www.ncbi.nlm.nih.gov/pubmed/34276766
http://dx.doi.org/10.3389/fgene.2021.651546
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author Ye, Zhenyao
Ke, Hongjie
Chen, Shuo
Cruz-Cano, Raul
He, Xin
Zhang, Jing
Dorgan, Joanne
Milton, Donald K.
Ma, Tianzhou
author_facet Ye, Zhenyao
Ke, Hongjie
Chen, Shuo
Cruz-Cano, Raul
He, Xin
Zhang, Jing
Dorgan, Joanne
Milton, Donald K.
Ma, Tianzhou
author_sort Ye, Zhenyao
collection PubMed
description With the increasing availability and dropping cost of high-throughput technology in recent years, many-omics datasets have accumulated in the public domain. Combining multiple transcriptomic studies on related hypothesis via meta-analysis can improve statistical power and reproducibility over single studies. For differential expression (DE) analysis, biomarker categorization by DE pattern across studies is a natural but critical task following biomarker detection to help explain between study heterogeneity and classify biomarkers into categories with potentially related functionality. In this paper, we propose a novel meta-analysis method to categorize biomarkers by simultaneously considering the concordant pattern and the biological and statistical significance across studies. Biomarkers with the same DE pattern can be analyzed together in downstream pathway enrichment analysis. In the presence of different types of transcripts (e.g., mRNA, miRNA, and lncRNA, etc.), integrative analysis including miRNA/lncRNA target enrichment analysis and miRNA-mRNA and lncRNA-mRNA causal regulatory network analysis can be conducted jointly on all the transcripts of the same category. We applied our method to two Pan-cancer transcriptomic study examples with single or multiple types of transcripts available. Targeted downstream analysis identified categories of biomarkers with unique functionality and regulatory relationships that motivate new hypothesis in Pan-cancer analysis.
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spelling pubmed-82836962021-07-17 Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies Ye, Zhenyao Ke, Hongjie Chen, Shuo Cruz-Cano, Raul He, Xin Zhang, Jing Dorgan, Joanne Milton, Donald K. Ma, Tianzhou Front Genet Genetics With the increasing availability and dropping cost of high-throughput technology in recent years, many-omics datasets have accumulated in the public domain. Combining multiple transcriptomic studies on related hypothesis via meta-analysis can improve statistical power and reproducibility over single studies. For differential expression (DE) analysis, biomarker categorization by DE pattern across studies is a natural but critical task following biomarker detection to help explain between study heterogeneity and classify biomarkers into categories with potentially related functionality. In this paper, we propose a novel meta-analysis method to categorize biomarkers by simultaneously considering the concordant pattern and the biological and statistical significance across studies. Biomarkers with the same DE pattern can be analyzed together in downstream pathway enrichment analysis. In the presence of different types of transcripts (e.g., mRNA, miRNA, and lncRNA, etc.), integrative analysis including miRNA/lncRNA target enrichment analysis and miRNA-mRNA and lncRNA-mRNA causal regulatory network analysis can be conducted jointly on all the transcripts of the same category. We applied our method to two Pan-cancer transcriptomic study examples with single or multiple types of transcripts available. Targeted downstream analysis identified categories of biomarkers with unique functionality and regulatory relationships that motivate new hypothesis in Pan-cancer analysis. Frontiers Media S.A. 2021-07-02 /pmc/articles/PMC8283696/ /pubmed/34276766 http://dx.doi.org/10.3389/fgene.2021.651546 Text en Copyright © 2021 Ye, Ke, Chen, Cruz-Cano, He, Zhang, Dorgan, Milton and Ma. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Ye, Zhenyao
Ke, Hongjie
Chen, Shuo
Cruz-Cano, Raul
He, Xin
Zhang, Jing
Dorgan, Joanne
Milton, Donald K.
Ma, Tianzhou
Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies
title Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies
title_full Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies
title_fullStr Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies
title_full_unstemmed Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies
title_short Biomarker Categorization in Transcriptomic Meta-Analysis by Concordant Patterns With Application to Pan-Cancer Studies
title_sort biomarker categorization in transcriptomic meta-analysis by concordant patterns with application to pan-cancer studies
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8283696/
https://www.ncbi.nlm.nih.gov/pubmed/34276766
http://dx.doi.org/10.3389/fgene.2021.651546
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