Evidence map›Paper›PMID 38798349›Full record

ArticlebioRxiv : the preprint server for biology2024

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 readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

5 · Who and what money

Authors and funding

11 authors.

Heming ZhangInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Dekang CaoInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Zirui ChenInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Xiuyuan ZhangInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Yixin ChenDepartment of Computer Science and Engineering, Washington University in St. Louis, St. Louis, MO, USA.
Cole SessionsDepartment of Pediatrics, Washington University in St. Louis, St. Louis, MO, USA.
Carlos CruchagaDepartment of Psychiatry, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-0276-2899
Philip PayneInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-9532-2998
Guangfu LiDepartment of Surgery, School of Medicine, University of Connecticut, CT, 06032, USA.
Michael ProvinceDivision of Statistical Genomics, Department of Genetics, Washington University in St. Louis, St. Louis, MO, USA.
Fuhai LiInstitute for Informatics, Data Science and Biostatistics (I2DB), Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.

Funding

Systems-Level Approach to Neuronopathic Lysosomal Storage DisordersRM1NS132962 · NINDS · WASHINGTON UNIVERSITY · PI JONATHAN D COOPER, PATRICIA I DICKSON · 2023 to 2026
$6.3M
Modeling and targeting tumor-immune signaling interactions in tumor microenvironmentR01LM013902 · NLM · WASHINGTON UNIVERSITY · PI Fuhai Li · 2023 to 2026
$1.4M
Combine Genomics and Symptoms Data Driven Models to Discover Synergistic Combinatory Therapies for Alzheimer's DiseaseR56AG065352 · NIA · WASHINGTON UNIVERSITY · PI LI, FUHAI · 2020 to 2021
$986k
AI models of multi-omic data integration for ming longevity core signaling pathwaysR21AG078799 · NIA · WASHINGTON UNIVERSITY · PI LI, FUHAI, PROVINCE, MICHAEL A. · 2023 to 2023
$461k
NIA NIH HHS R21 AG078799NIA NIH HHS R56 AG065352NINDS NIH HHS RM1 NS132962NLM NIH HHS R01 LM013902
6 · The paper itself

Abstract

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 key disease targets and signaling pathways. 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. However, it is non-trivial 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. To resolve this challenge, we developed

Identifiers

PMID38798349
PMCPMC11118290

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.