ArticleBioinformatics (Oxford, England)2026
Reconstructing cell-cell interaction network in single-cell spatial transcriptomics via directed heterogeneous graph autoencoder.
Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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
2 citing papers in PubMed.
- Machine learning and computational approaches to model therapeutic response and resistance in diffuse midline glioma.Journal of neuro-oncology · 2026Review
- PlantCCC prioritizes context-specific candidate ligand-receptor communication patterns in plant spatial transcriptomics.Plant molecular biology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
motivationSpatial transcriptome data have both gene expression information and cell spatial location information, offering exceptional prospects for analyzing cell-cell interaction (CCI) network. Most existing statistical and optimal transport-based methods rely only on known ligand-receptor pairs to infer CCI network. Furthermore, most current deep learning frameworks rely on symmetric decoders or undirected graph architectures.
resultsTaking advantage of spatial transcriptomic data and graph autoencoders, we present a directed heterogeneous graph autoencoder-based approach DualCellChat to reconstruct a complete and accurate CCI network from incomplete single cell spatial transcriptomics. Benchmarked on five single-cell spatial datasets from four different technologies, we demonstrate that DualCellChat outperforms existing deep learning-based methods and can inherently model the direction of cellular interactions. Furthermore, we introduce downstream analysis to infer signature genes involved in cellular interactions from the reconstructed CCI network and infer significant ligand-receptor pairs for specific cell types. AVAILABILITY AND IMPLEMENTATION: The dataset and code are available in GitHub (https://github.com/JinxianHu/DualCellChat) and Zenodo (DOI: 10.5281/zenodo.18512678).
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.