Saved in:
Bibliographic Details
Main Authors: Mosleth, Ellen Færgestad, Dankel, Simon Erling Nitter, Mellgren, Gunnar, Olmos, Francisco Martin Barajas, Orozco, Lorena Sofia, Lysenko, Artem, Ofstad, Ragni, Begum, Most Champa, Martens, Harald, Liland, Kristian Hovde
Format: Preprint
Published: 2024
Subjects:
Online Access:https://arxiv.org/abs/2404.03029
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866913299297206272
author Mosleth, Ellen Færgestad
Dankel, Simon Erling Nitter
Mellgren, Gunnar
Olmos, Francisco Martin Barajas
Orozco, Lorena Sofia
Lysenko, Artem
Ofstad, Ragni
Begum, Most Champa
Martens, Harald
Liland, Kristian Hovde
author_facet Mosleth, Ellen Færgestad
Dankel, Simon Erling Nitter
Mellgren, Gunnar
Olmos, Francisco Martin Barajas
Orozco, Lorena Sofia
Lysenko, Artem
Ofstad, Ragni
Begum, Most Champa
Martens, Harald
Liland, Kristian Hovde
contents General Effect Modelling (GEM) is an umbrella over different methods that utilise effects in the analyses of data with multiple design variables and multivariate responses. To demonstrate the methodology, we here use GEM in gene expression data where we use GEM to combine data from different cohorts and apply multivariate analysis of the effects of the targeted disease across the cohorts. Omics data are by nature multivariate, yet univariate analysis is the dominating approach used for such data. A major challenge in omics data is that the number of features such as genes, proteins and metabolites are often very large, whereas the number of samples is limited. Furthermore, omics research aims to obtain results that are generically valid across different backgrounds. The present publication applies GEM to address these aspects. First, we emphasise the benefit of multivariate analysis for multivariate data. Then we illustrate the use of GEM to combine data from two different cohorts for multivariate analysis across the cohorts, and we highlight that multivariate analysis can detect information that is lost by univariate validation.
format Preprint
id arxiv_https___arxiv_org_abs_2404_03029
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle General Effect Modelling (GEM) -- Part 2. Multivariate GEM applied to gene expression data of type 2 diabetes detects information that is lost by univariate validation
Mosleth, Ellen Færgestad
Dankel, Simon Erling Nitter
Mellgren, Gunnar
Olmos, Francisco Martin Barajas
Orozco, Lorena Sofia
Lysenko, Artem
Ofstad, Ragni
Begum, Most Champa
Martens, Harald
Liland, Kristian Hovde
Methodology
Applications
General Effect Modelling (GEM) is an umbrella over different methods that utilise effects in the analyses of data with multiple design variables and multivariate responses. To demonstrate the methodology, we here use GEM in gene expression data where we use GEM to combine data from different cohorts and apply multivariate analysis of the effects of the targeted disease across the cohorts. Omics data are by nature multivariate, yet univariate analysis is the dominating approach used for such data. A major challenge in omics data is that the number of features such as genes, proteins and metabolites are often very large, whereas the number of samples is limited. Furthermore, omics research aims to obtain results that are generically valid across different backgrounds. The present publication applies GEM to address these aspects. First, we emphasise the benefit of multivariate analysis for multivariate data. Then we illustrate the use of GEM to combine data from two different cohorts for multivariate analysis across the cohorts, and we highlight that multivariate analysis can detect information that is lost by univariate validation.
title General Effect Modelling (GEM) -- Part 2. Multivariate GEM applied to gene expression data of type 2 diabetes detects information that is lost by univariate validation
topic Methodology
Applications
url https://arxiv.org/abs/2404.03029