ReviewBriefings in bioinformatics2026
Multimodal bioinformatic analyses of genome-scale expression beyond gene-centric differential expression.
Review in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Genome-scale gene expression analysis has become a standard approach for discovering biomarkers and understanding molecular mechanisms. Recent advances in omics technologies now enable investigations beyond conventional case-control comparison and standard gene-centric differential expression (DE) analyses. In this review, we highlight conceptual and methodological advances in using transcriptomic and multimodal omic data to elucidate diverse mechanisms of gene expression. We first provide a comprehensive overview of different types of gene expression study designs, along with suitable statistical testing, as well as key considerations. We then describe strategies for inferring gene co-expression and regulatory networks, with particular emphasis on context-specific network models and machine learning methods that capture the multifactorial nature of gene expression regulation. Finally, we present perspectives on emerging modalities such as single-cell and spatial transcriptomics, which enable unprecedented resolution in mapping regulatory complexity. We envisage that the concepts and examples described here will raise awareness and encourage the application of advanced network-based analyses.
Indexed as
Identifiers
What Socratic 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 Socratic graph.