Evidence map›Paper›PMID 29977361›Full record

ArticleExperimental and therapeutic medicine2018

Identification of differential modules in ankylosing spondylitis using systemic module inference and the attract method.

Fang-Chang Yuan, Bo Li, Li-Jun Zhang

Abstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Fang-Chang YuanDepartment of Orthopedics, People's Hospital of Rizhao, Rizhao, Shandong 276826, P.R. China.
Bo LiDepartment of Joint Surgery, Hospital of Xinjiang Production and Construction Corps, Urumchi, Xinjiang Uygur Autonomous Region 830002, P.R. China.
Li-Jun ZhangDepartment of Orthopedics, The Fifth People's Hospital of Jinan, Jinan, Shandong 250022, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of the present study was to identify differential modules in ankylosing spondylitis (AS) by integrating network analysis, module inference and the attract method. To achieve this objective, four steps were conducted. The first step was disease objective network (DON) for AS, and healthy objective network (HON) inference dependent on gene expression data, protein-protein interaction networks and Spearman's correlation coefficient. In the second step, module detection was performed by utilizing a clique-merging algorithm, which comprised of exploring maximal cliques by clique algorithm and refining or merging maximal cliques with a high overlap. The third part was seed module evaluation through module pair matches by Jaccard score and module correlation density (MCD) calculation. Finally, in the fourth step, differential modules between the AS and healthy groups were identified based on a gene set enrichment analysis-analysis of variance model in the attract method. There were 5,301 nodes and 28,176 interactions both in DON and HON. A total of 20 and 21 modules were detected for the AS and healthy group, respectively. Notably, six seed modules across two groups were identified with Jaccard score ≥0.5, and these were ranked in descending order of differential MCD (Δ

Indexed as

ankylosing spondylitisattractmodulenetwork

Identifiers

PMID29977361
PMCPMC6030912

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