ArticleMicroarrays (Basel, Switzerland)2013
Evaluation of Different Normalization and Analysis Procedures for Illumina Gene Expression Microarray Data Involving Small Changes.
Article in Microarrays (Basel, Switzerland), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- An Epigenomic Meta-Analysis of Differentially Methylated Sites in Pre- and Post-Metabolic/Bariatric Surgery Adult Female Patients.Epigenomes · 2025Review
- Systematic Evaluation of Normalization Methods for Glycomics Data Based on Performance of Network Inference.Metabolites · 2020Article
- Article
- Genetically unmatched human iPSC and ESC exhibit equivalent gene expression and neuronal differentiation potential.Scientific reports · 2017Article
- Brain iron accumulation affects myelin-related molecular systems implicated in a rare neurogenetic disease family with neuropsychiatric features.Molecular psychiatry · 2016Article
- Advantages of Array-Based Technologies for Pre-Emptive Pharmacogenomics Testing.Microarrays (Basel, Switzerland) · 2016Review
- Gene co-expression networks shed light into diseases of brain iron accumulation.Neurobiology of disease · 2016Article
- Pathological relationships involving iron and myelin may constitute a shared mechanism linking various rare and common brain diseases.Rare diseases (Austin, Tex.) · 2016Article
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Authors and funding
10 authors.
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Abstract
While Illumina microarrays can be used successfully for detecting small gene expression changes due to their high degree of technical replicability, there is little information on how different normalization and differential expression analysis strategies affect outcomes. To evaluate this, we assessed concordance across gene lists generated by applying different combinations of normalization strategy and analytical approach to two Illumina datasets with modest expression changes. In addition to using traditional statistical approaches, we also tested an approach based on combinatorial optimization. We found that the choice of both normalization strategy and analytical approach considerably affected outcomes, in some cases leading to substantial differences in gene lists and subsequent pathway analysis results. Our findings suggest that important biological phenomena may be overlooked when there is a routine practice of using only one approach to investigate all microarray datasets. Analytical artefacts of this kind are likely to be especially relevant for datasets involving small fold changes, where inherent technical variation-if not adequately minimized by effective normalization-may overshadow true biological variation. This report provides some basic guidelines for optimizing outcomes when working with Illumina datasets involving small expression changes.
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