ArticleBMC bioinformatics2016
A comparative evaluation of data-merging and meta-analysis methods for reconstructing gene-gene interactions.
Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
16 citing papers in PubMed, 28 citations in OpenAlex.
- A Cross-Region Meta-Analysis and Machine Learning Identifies a 37-Gene Signature Associated with Alzheimer's Disease.Biomedicines · 2026Article
- Meta-Merging the Transcriptomes of Gastric Tumors Redefines the Connections among Molecular and Clinical Subtypes.Asian Pacific journal of cancer prevention : APJCP · 2026Article
- Sex-Specific Prediction Models of Alzheimer's Disease: A Gene Expression Analysis.International journal of medical sciences · 2026Article
- Glycosylation gene-based molecular recognition model for diabetic retinopathy.Frontiers in medicine · 2026Article
- Article
- Machine learning-based identification of core regulatory genes in hepatocellular carcinoma: insights from lactylation modification and liver regeneration-related genes.Frontiers in oncology · 2025Article
- A robust transfer learning approach for high-dimensional linear regression to support integration of multi-source gene expression data.PLoS computational biology · 2025Article
- Reposition: Focalizing β-Alanine Metabolism and the Anti-Inflammatory Effects of Its Metabolite Based on Multi-Omics Datasets.International journal of molecular sciences · 2024Article
- Article
- Uniformly shaped harmonization combines human transcriptomic data from different platforms while retaining their biological properties and differential gene expression patterns.Frontiers in molecular biosciences · 2023Article
- Interpretable Machine Learning Reveals Dissimilarities Between Subtypes of Autism Spectrum Disorder.Frontiers in genetics · 2021Article
- Evidence for shared molecular pathways of dysregulated decidualization in preeclampsia and endometrial disorders revealed by microarray data integration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019Article
- Elucidation of the sequential transcriptional activity in Escherichia coli using time-series RNA-seq data.Bioinformation · 2017Article
- Erratum to: A comparative evaluation of data-merging and meta-analysis methods for reconstructing gene-gene interactions.BMC bioinformatics · 2016Article
- omicsNPC: Applying the Non-Parametric Combination Methodology to the Integrative Analysis of Heterogeneous Omics Data.PloS one · 2016Article
- Feature selection with the R packageF1000ResearchArticle
Corrections and comments
- Erratum issued
Authors and funding
5 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundWe address the problem of integratively analyzing multiple gene expression, microarray datasets in order to reconstruct gene-gene interaction networks. Integrating multiple datasets is generally believed to provide increased statistical power and to lead to a better characterization of the system under study. However, the presence of systematic variation across different studies makes network reverse-engineering tasks particularly challenging. We contrast two approaches that have been frequently used in the literature for addressing systematic biases: meta-analysis methods, which first calculate opportune statistics on single datasets and successively summarize them, and data-merging methods, which directly analyze the pooled data after removing eventual biases. This comparative evaluation is performed on both synthetic and real data, the latter consisting of two manually curated microarray compendia comprising several E. coli and Yeast studies, respectively. Furthermore, the reconstruction of the regulatory network of the transcription factor Ikaros in human Peripheral Blood Mononuclear Cells (PBMCs) is presented as a case-study.
resultsThe meta-analysis and data-merging methods included in our experimentations provided comparable performances on both synthetic and real data. Furthermore, both approaches outperformed (a) the naïve solution of merging data together ignoring possible biases, and (b) the results that are expected when only one dataset out of the available ones is analyzed in isolation. Using correlation statistics proved to be more effective than using p-values for correctly ranking candidate interactions. The results from the PBMC case-study indicate that the findings of the present study generalize to different types of network reconstruction algorithms.
conclusionsIgnoring the systematic variations that differentiate heterogeneous studies can produce results that are statistically indistinguishable from random guessing. Meta-analysis and data merging methods have proved equally effective in addressing this issue, and thus researchers may safely select the approach that best suit their specific application.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.