Evidence map›Paper›PMID 39506989›Full record

ArticleBioinformatics advances2024

mosGraphGen: a novel tool to generate multi-omics signaling graphs to facilitate integrative and interpretable graph AI model development.

Heming Zhang, Dekang Cao, Zirui Chen, Xiuyuan Zhang, Yixin Chen, Cole Sessions, Carlos Cruchaga, Philip Payne, Guangfu Li, Michael Province and 1 more

Abstract read
In one paragraph

Article in Bioinformatics advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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  3. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Heming ZhangInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.ORCID https://orcid.org/0000-0002-2025-9090
Dekang CaoInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.
Zirui ChenInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.
Xiuyuan ZhangInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.
Yixin ChenDepartment of Computer Science and Engineering, Washington University in St. Louis, Saint Louis, MO 63130, United States.
Cole SessionsDepartment of Pediatrics, Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.
Carlos CruchagaDepartment of Psychiatry, Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.
Philip PayneInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.ORCID https://orcid.org/0000-0002-9532-2998
Guangfu LiDepartment of Surgery, School of Medicine, University of Connecticut, Farmington, CT 06030, United States.
Michael ProvinceDivision of Statistical Genomics, Department of Genetics, Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.
Fuhai LiInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Saint Louis, MO 63110-1010, United States.ORCID https://orcid.org/0000-0002-3773-146X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Multi-omics data, i.e. genomics, epigenomics, transcriptomics, proteomics, characterize cellular complex signaling systems from multi-level and multi-view and provide a holistic view of complex cellular signaling pathways. However, it remains challenging to integrate and interpret multi-omics data for mining critical biomarkers. Graph AI models have been widely used to analyze graph-structure datasets, and are ideal for integrative multi-omics data analysis because they can naturally integrate and represent multi-omics data as a biologically meaningful multi-level signaling graph and interpret multi-omics data via graph node and edge ranking analysis. Nevertheless, it is nontrivial for graph-AI model developers to pre-analyze multi-omics data and convert the data into biologically meaningful graphs, which can be directly fed into graph-AI models. Results: To resolve this challenge, we developed mosGraphGen (multi-omics signaling graph generator), generating Multi-omics Signaling graphs (mos-graph) of individual samples by mapping multi-omics data onto a biologically meaningful multi-level background signaling network with data normalization by aggregating measurements and aligning to the reference genome. With mosGraphGen, AI model developers can directly apply and evaluate their models using these mos-graphs. In the results, mosGraphGen was used and illustrated using two widely used multi-omics datasets of The Cancer Genome Atlas (TCGA) and Alzheimer's disease (AD) samples. Availability and implementation: The code of mosGraphGen is open-source and publicly available via GitHub: https://github.com/FuhaiLiAiLab/mosGraphGen.

Identifiers

PMID39506989
PMCPMC11540438

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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 Socratic graph.