Evidence map›Paper›PMID 40843971›Full record

ArticleBriefings in bioinformatics2025

Boosting data interpretation with GIBOOST to enhance visualization of complex high-dimensional data.

Komlan Atitey, Jiaqi Li, Brian Papas, Osafu A Egbon, Jian-Liang Li, Musa Kana, Idowu Aimola, Benedict Anchang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Komlan AtiteyBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, 111 T W Alexander Dr, Research Triangle Park, Durham, NC 27709, United States.
Jiaqi LiBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, 111 T W Alexander Dr, Research Triangle Park, Durham, NC 27709, United States.
Brian PapasBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, 111 T W Alexander Dr, Research Triangle Park, Durham, NC 27709, United States.
Osafu A EgbonBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, 111 T W Alexander Dr, Research Triangle Park, Durham, NC 27709, United States.
Jian-Liang LiBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, 111 T W Alexander Dr, Research Triangle Park, Durham, NC 27709, United States.ORCID 0000-0002-6487-081X
Musa KanaDepartment of Community Medicine, Faculty of Clinical Sciences, College of Medicine, Kaduna State University, Tafawa Balewa Way, Kaduna, Kaduna State, 800241, Nigeria.
Idowu AimolaAfrica Centre of Excellence for Neglected Tropical Diseases and Forensic Biotechnology, Department of Biochemistry, Ahmadu Bello University, Sokoto Road, Zaria, 800001, Nigeria.
Benedict AnchangBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, 111 T W Alexander Dr, Research Triangle Park, Durham, NC 27709, United States.ORCID 0000-0002-5576-5647

Funding

Single-cell Analysis of Normal and Perturbed Dynamic Biological SystemsZIAES103350 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI ANCHANG, BENEDICT · 2020 to 2025
$3.5M
Intramural NIH HHS ZIA ES103350NIH/NIEHS/DIR and from Chan Zuckerberg Initiative DAF 1ZIAES103350-05Silicon Valley Community Foundation 2021-240134 (5022)
6 · The paper itself

Abstract

High-dimensional single-cell data analysis is crucial for understanding complex biological interactions, yet conventional dimensionality reduction methods (DRMs) often fail to preserve both global and local structures. Existing DRMs, such as t-distributed Stochastic Neighbor Embedding (t-SNE), Uniform Manifold Approximation and Projection (UMAP), Principal Component Analysis (PCA), and Potential of Heat-diffusion for Affinity-based Transition Embedding (PHATE), optimize different visualization objectives, resulting in trade-offs between cluster separability, spatial organization, and temporal coherence. To overcome these limitations, we introduce GIBOOST, an AI-driven framework that integrates outputs from multiple DRMs using a Bayesian framework and an optimized autoencoder. GIBOOST systematically selects and integrates the two most informative DRMs by evaluating key visualization features, including separability, spatial continuity, uniformity, cellular dynamics, and cluster sensitivity. Rather than prioritizing a single DRM, it identifies the optimal combination that maximizes clustering sensitivity (GI) while preserving biologically relevant spatial and temporal structures. This integration is further refined through a GI-optimized autoencoder, which optimizes the joint distribution of GI, neuron count, and batch size effects to improve visualization quality. We demonstrate GIBOOST's efficacy across multiple dynamic biological processes, including epithelial-mesenchymal transition, CiPSC reprogramming, spermatogenesis, and placental development. Compared to nine individual DRMs, GIBOOST enhances clustering sensitivity and biological relevance by ~30%, enabling more accurate interpretation of differentiation trajectories and cell-cell interactions. When applied to a large single-cell RNA-seq dataset (~400 000 cells, 28 cell types, seven placental regions), GIBOOST uncovers novel immune-placenta interactions, providing deeper insights into cross-tissue communication during pregnancy. By improving both the visualization and interpretability of high-dimensional data, GIBOOST serves as a powerful tool for computational systems biology, enabling a more accurate exploration of complex cellular systems.

Indexed as

Computational BiologySingle-Cell AnalysisSoftwareAlgorithmsBayes TheoremFemaleHumansPregnancyAI-driven data integrationcell–cell communicationdata visualizationdimensionality reductionimmune-placental interactionssingle-cell analysis

Identifiers

PMID40843971
PMCPMC12371410

What OpenQuestion holds

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Registered trials

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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.