Evidence map›Paper›PMID 33905111›Full record

ArticleInterdisciplinary sciences, computational life sciences2021

A New Framework for Discovering Protein Complex and Disease Association via Mining Multiple Databases.

Lei Xue, Xu-Qing Tang

Abstract read
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In one paragraph

Article in Interdisciplinary sciences, computational life sciences, 2021. 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
0.2field-weighted citation impact, top 52% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 1 institution in 1 country.

Lei XueSchool of Science, Jiangnan University, Wuxi, 214122, China.
Xu-Qing TangSchool of Science, Jiangnan University, Wuxi, 214122, China. txq5139@jiangnan.edu.cn.ORCID http://orcid.org/0000-0002-4018-9114
Jiangnan University · CN

Funding

National Natural Science Foundation of China 11371174
6 · The paper itself

Abstract

One important challenge in the post-genomic era is to explore disease mechanisms by efficiently integrating different types of biological data. In fact, a single disease is usually caused through multiple genes products such as protein complexes rather than single gene. Therefore, it is meaningful for us to discover protein communities from the protein-protein interaction network and use them for inferring disease-disease associations. In this article, we propose a new framework including protein-protein networks, disease-gene associations and disease-complex pairs to cluster protein complexes and infer disease associations. Complexes discovered by our approach is superior in quality (Sn, PPV and ACC) and clustering quantity than other four popular methods on three PPI networks. A systematic analysis shows that disease pairs sharing more protein complexes (such as Glucose and Lipid Metabolic Disorders) are more similar and overlapping proteins may have different roles in different diseases. These findings can provide clinical scholars and medical practitioners with new ideas on disease identification and treatment.

Indexed as

AlgorithmsProtein Interaction MappingCluster AnalysisDatabases, ProteinProtein Interaction MapsProteinsProteinsCommunity detectionDisease associationLocal expansionOverlapping protein complexProtein–protein network

Identifiers

PMID33905111
OpenAlexW3157788980

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.