ArticlePLoS computational biology2025
Branch-specific gene discovery in cell differentiation using multi-omics graph attention.
Article in PLoS computational biology, 2025. 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.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Understanding gene regulation during cell differentiation requires effective integration of multi-omics single-cell data. In this study, we propose BranchKGN, a heterogeneous graph transformer-based framework for identifying branch-specific key genes along cell differentiation trajectories. By integrating scRNA-seq and scATAC-seq data into a unified gene representation, we infer differentiation trajectories using Slingshot and construct a heterogeneous graph capturing gene-cell relationships. Through attention-based graph learning, BranchKGN assigns gene importance scores within each cell, enabling the identification of genes consistently informative across branch point cells and their descendant lineages. These genes are then used to reconstruct gene regulatory networks and differentiation trajectories. Validation on three independent datasets demonstrates that the identified gene sets not only capture key regulators of cell fate bifurcation but also support accurate reconstruction of differentiation trajectories. Our results highlight the effectiveness of BranchKGN in dissecting gene regulation dynamics during cellular transitions and provide a valuable tool for multi-omics single-cell analysis.
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.