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Guided extraction of genome-scale metabolic models for the integration and analysis of omics data
ID
Walakira, Andrew
(
Author
),
ID
Rozman, Damjana
(
Author
),
ID
Režen, Tadeja
(
Author
),
ID
Mraz, Miha
(
Author
),
ID
Moškon, Miha
(
Author
)
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https://www.sciencedirect.com/science/article/pii/S2001037021002476
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Abstract
Omics data can be integrated into a reference model using various model extraction methods (MEMs) to yield context-specific genome-scale metabolic models (GEMs). How to chose the appropriate MEM, thresholding rule and threshold remains a challenge. We integrated mouse transcriptomic data from a Cyp51 knockout mice diet experiment (GSE58271) using five MEMs (GIMME, iMAT, FASTCORE, INIT an tINIT) in a combination with a recently published mouse GEM iMM1865. Except for INIT and tINIT, the size of extracted models varied with the MEM used (t-test: p-value <0.001). The Jaccard index of iMAT models ranged from 0.27 to 1.0. Out of the three factors under study in the experiment (diet, gender and genotype), gender explained most of the variability (>90%) in PC1 for FASTCORE. In iMAT, each of the three factors explained less than 40% of the variability within PC1, PC2 and PC3. Among all the MEMs, FASTCORE captured the most of the true variability in the data by clustering samples by gender. Our results show that for the efficient use of MEMs in the context of omics data integration and analysis, one should apply various MEMs, thresholding rules, and thresholding values to select the MEM and its configuration that best captures the true variability in the data. This selection can be guided by the methodology as proposed and used in this paper. Moreover, we describe certain approaches that can be used to analyse the results obtained with the selected MEM and to put these results in a biological context.
Language:
English
Keywords:
genome-scale metabolic model
,
model extraction methods
,
context-specific metabolic model
,
omics data integration
,
subsystem enrichment analysis
,
model interpretability
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
MF - Faculty of Medicine
FRI - Faculty of Computer and Information Science
Publication status:
Published
Publication version:
Version of Record
Year:
2021
Number of pages:
Str. 3521-3530
Numbering:
Vol. 19
PID:
20.500.12556/RUL-127776
UDC:
004:575.112
ISSN on article:
2001-0370
DOI:
10.1016/j.csbj.2021.06.009
COBISS.SI-ID:
66227971
Publication date in RUL:
22.06.2021
Views:
2008
Downloads:
247
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Record is a part of a journal
Title:
Computational and structural biotechnology journal
Publisher:
Elsevier, Research Network of Computational and Structural Biotechnology
ISSN:
2001-0370
COBISS.SI-ID:
5068826
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
metabolni modeli na nivoju genoma
,
ekstrakcija modelov
,
kontekstno specifični metabolni modeli
,
integracija omskih podatkov
,
analiza obogatitve metabolnih podsistemov
Projects
Funder:
EC - European Commission
Funding programme:
H2020
Project number:
860895
Name:
Translational SYStemics: Personalised Medicine at the Interface of Translational Research and Systems Medicine
Acronym:
TranSYS
Funder:
ARRS - Slovenian Research Agency
Project number:
P2-0359
Name:
Vseprisotno računalništvo
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0390
Name:
Funkcijska genomika in biotehnologija za zdravje
Funder:
ARRS - Slovenian Research Agency
Project number:
J1-9176
Name:
HolesteROR pri presnovnih boleznih jeter
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