Evidence map›Paper›PMID 38218959›Full record

ArticleNPJ systems biology and applications2024

GINv2.0: a comprehensive topological network integrating molecular interactions from multiple knowledge bases.

Xiao Chang, Shen Yan, Yizheng Zhang, Yingchun Zhang, Luyang Li, Zhanyu Gao, Xuefei Lin, Xu Chi

Open access · goldAbstract read
In one paragraph

Article in NPJ systems biology and applications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 39% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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 at 3 institutions in 1 country.

Xiao Chang *Department of Dermatology and Venereal Disease, Xuan Wu Hospital, Beijing, 100053, China.ORCID http://orcid.org/0009-0001-2727-4410
Shen Yan *Agricultural Information Institute, Chinese Academy of Agricultural Science, Beijing, 100081, China.ORCID http://orcid.org/0000-0002-9236-9483
Yizheng ZhangCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, 100101, China.ORCID http://orcid.org/0009-0007-8657-8063
Yingchun ZhangKey Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.ORCID http://orcid.org/0009-0009-3925-0107
Luyang LiCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, 100101, China.ORCID http://orcid.org/0009-0000-2801-8817
Zhanyu GaoCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, 100101, China.ORCID http://orcid.org/0009-0005-5292-5608
Xuefei LinDepartment of Dermatology and Venereal Disease, Xuan Wu Hospital, Beijing, 100053, China.ORCID http://orcid.org/0009-0004-0793-9552
Xu ChiCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, 100101, China. chix@big.ac.cn.ORCID http://orcid.org/0000-0002-6434-6882
Chinese Academy of Sciences · CNXuan Wu Hospital of the Capital Medical University · CNAgricultural Information Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knowledge bases have been instrumental in advancing biological research, facilitating pathway analysis and data visualization, which are now widely employed in the scientific community. Despite the establishment of several prominent knowledge bases focusing on signaling, metabolic networks, or both, integrating these networks into a unified topological network has proven to be challenging. The intricacy of molecular interactions and the diverse formats employed to store and display them contribute to the complexity of this task. In a prior study, we addressed this challenge by introducing a "meta-pathway" structure that integrated the advantages of the Simple Interaction Format (SIF) while accommodating reaction information. Nevertheless, the earlier Global Integrative Network (GIN) was limited to reliance on KEGG alone. Here, we present GIN version 2.0, which incorporates human molecular interaction data from ten distinct knowledge bases, including KEGG, Reactome, and HumanCyc, among others. We standardized the data structure, gene IDs, and chemical IDs, and conducted a comprehensive analysis of the consistency among the ten knowledge bases before combining all unified interactions into GINv2.0. Utilizing GINv2.0, we investigated the glycolysis process and its regulatory proteins, revealing coordinated regulations on glycolysis and autophagy, particularly under glucose starvation. The expanded scope and enhanced capabilities of GINv2.0 provide a valuable resource for comprehensive systems-level analyses in the field of biological research. GINv2.0 can be accessed at: https://github.com/BIGchix/GINv2.0 .

Indexed as

Metabolic Networks and PathwaysSignal TransductionHumansKnowledge Bases

Identifiers

PMID38218959
PMCPMC10787761
OpenAlexW4390840707

What Socratic holds

Textmetadata
LicenceCC BY
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.