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NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data

Biological processes (like microbial growth & physiological response) are usually dynamic and require the monitoring of metabolic variation at different time-points. Moreover, there is clear shift from case-control (N=2) study to multi-class (N>2) problem in current metabolomics, which is cru...

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Autores principales: Yang, Qingxia, Wang, Yunxia, Zhang, Ying, Li, Fengcheng, Xia, Weiqi, Zhou, Ying, Qiu, Yunqing, Li, Honglin, Zhu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319444/
https://www.ncbi.nlm.nih.gov/pubmed/32324219
http://dx.doi.org/10.1093/nar/gkaa258
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author Yang, Qingxia
Wang, Yunxia
Zhang, Ying
Li, Fengcheng
Xia, Weiqi
Zhou, Ying
Qiu, Yunqing
Li, Honglin
Zhu, Feng
author_facet Yang, Qingxia
Wang, Yunxia
Zhang, Ying
Li, Fengcheng
Xia, Weiqi
Zhou, Ying
Qiu, Yunqing
Li, Honglin
Zhu, Feng
author_sort Yang, Qingxia
collection PubMed
description Biological processes (like microbial growth & physiological response) are usually dynamic and require the monitoring of metabolic variation at different time-points. Moreover, there is clear shift from case-control (N=2) study to multi-class (N>2) problem in current metabolomics, which is crucial for revealing the mechanisms underlying certain physiological process, disease metastasis, etc. These time-course and multi-class metabolomics have attracted great attention, and data normalization is essential for removing unwanted biological/experimental variations in these studies. However, no tool (including NOREVA 1.0 focusing only on case-control studies) is available for effectively assessing the performance of normalization method on time-course/multi-class metabolomic data. Thus, NOREVA was updated to version 2.0 by (i) realizing normalization and evaluation of both time-course and multi-class metabolomic data, (ii) integrating 144 normalization methods of a recently proposed combination strategy and (iii) identifying the well-performing methods by comprehensively assessing the largest set of normalizations (168 in total, significantly larger than those 24 in NOREVA 1.0). The significance of this update was extensively validated by case studies on benchmark datasets. All in all, NOREVA 2.0 is distinguished for its capability in identifying well-performing normalization method(s) for time-course and multi-class metabolomics, which makes it an indispensable complement to other available tools. NOREVA can be accessed at https://idrblab.org/noreva/.
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spelling pubmed-73194442020-07-01 NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data Yang, Qingxia Wang, Yunxia Zhang, Ying Li, Fengcheng Xia, Weiqi Zhou, Ying Qiu, Yunqing Li, Honglin Zhu, Feng Nucleic Acids Res Web Server Issue Biological processes (like microbial growth & physiological response) are usually dynamic and require the monitoring of metabolic variation at different time-points. Moreover, there is clear shift from case-control (N=2) study to multi-class (N>2) problem in current metabolomics, which is crucial for revealing the mechanisms underlying certain physiological process, disease metastasis, etc. These time-course and multi-class metabolomics have attracted great attention, and data normalization is essential for removing unwanted biological/experimental variations in these studies. However, no tool (including NOREVA 1.0 focusing only on case-control studies) is available for effectively assessing the performance of normalization method on time-course/multi-class metabolomic data. Thus, NOREVA was updated to version 2.0 by (i) realizing normalization and evaluation of both time-course and multi-class metabolomic data, (ii) integrating 144 normalization methods of a recently proposed combination strategy and (iii) identifying the well-performing methods by comprehensively assessing the largest set of normalizations (168 in total, significantly larger than those 24 in NOREVA 1.0). The significance of this update was extensively validated by case studies on benchmark datasets. All in all, NOREVA 2.0 is distinguished for its capability in identifying well-performing normalization method(s) for time-course and multi-class metabolomics, which makes it an indispensable complement to other available tools. NOREVA can be accessed at https://idrblab.org/noreva/. Oxford University Press 2020-07-02 2020-04-23 /pmc/articles/PMC7319444/ /pubmed/32324219 http://dx.doi.org/10.1093/nar/gkaa258 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Web Server Issue
Yang, Qingxia
Wang, Yunxia
Zhang, Ying
Li, Fengcheng
Xia, Weiqi
Zhou, Ying
Qiu, Yunqing
Li, Honglin
Zhu, Feng
NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data
title NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data
title_full NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data
title_fullStr NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data
title_full_unstemmed NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data
title_short NOREVA: enhanced normalization and evaluation of time-course and multi-class metabolomic data
title_sort noreva: enhanced normalization and evaluation of time-course and multi-class metabolomic data
topic Web Server Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319444/
https://www.ncbi.nlm.nih.gov/pubmed/32324219
http://dx.doi.org/10.1093/nar/gkaa258
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