Evidence map›Paper›PMID 29533218›Full record

ArticleIET systems biology2018

SMILE: a novel procedure for subcellular module identification with localisation expansion.

Lixin Cheng, Pengfei Liu, Kwong-Sak Leung

Abstract read
In one paragraph

Article in IET systems biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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  14. Biochemical pathway analysis of gastric atrophy.Gastroenterology and hepatology from bed to bench · 2018
    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

3 authors.

Lixin ChengDepartment of Computer Science & Engineering, Chinese University of Hong Kong, Ma Liu Shui, Hong Kong.
Pengfei LiuDepartment of Computer Science & Engineering, Chinese University of Hong Kong, Ma Liu Shui, Hong Kong.
Kwong-Sak LeungDepartment of Computer Science & Engineering, Chinese University of Hong Kong, Ma Liu Shui, Hong Kong. ksleung@cse.cuhk.edu.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Computational clustering methods help identify functional modules in protein-protein interaction (PPI) network, in which proteins participate in the same biological pathways or specific functions. Subcellular localisation is crucial for proteins to implement biological functions and each compartment accommodates specific portions of the protein interaction structure. However, the importance of protein subcellular localisation is often neglected in the studies of module identification. In this study, the authors propose a novel procedure, subcellular module identification with localisation expansion (SMILE), to identify super modules that consist of several subcellular modules performing specific biological functions among cell compartments. These super modules identified by SMILE are more functionally diverse and have been verified to be more associated with known protein complexes and biological pathways compared with the modules identified from the global PPI networks in both the compartmentalised PPI and InWeb_InBioMap datasets. The authors' results reveal that subcellular localisation is a principal feature of functional modules and offers important guidance in detecting biologically meaningful results.

Indexed as

Cluster AnalysisProtein Interaction MapsAlgorithmsProtein Interaction MappingProteinsProteins

Identifiers

PMID29533218
PMCPMC8687326

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Registered trials

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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 OpenQuestion graph.