Evidence map›Paper›PMID 29045465›Full record

ArticlePloS one2017

Identifying protein complex by integrating characteristic of core-attachment into dynamic PPI network.

Xianjun Shen, Li Yi, Xingpeng Jiang, Tingting He, Jincai Yang, Wei Xie, Po Hu, Xiaohua Hu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. 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 1 institution in 2 countries.

Xianjun ShenSchool of Computer, Central China Normal University, Wuhan, China.
Li YiSchool of Computer, Central China Normal University, Wuhan, China.ORCID http://orcid.org/0000-0001-5545-7663
Xingpeng JiangSchool of Computer, Central China Normal University, Wuhan, China.
Tingting HeSchool of Computer, Central China Normal University, Wuhan, China.
Jincai YangSchool of Computer, Central China Normal University, Wuhan, China.
Wei XieSchool of Computer, Central China Normal University, Wuhan, China.
Po HuSchool of Computer, Central China Normal University, Wuhan, China.
Xiaohua HuSchool of Computer, Central China Normal University, Wuhan, China.
Central China Normal University · CN

Funding

Neuropsychological and Thyroid Effects of PBDEsR01TS000003 · TS · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI FITZGERALD, EDWARD F · 2004 to 2006
$185k
ATSDR CDC HHS R01 TS000003
6 · The paper itself

Abstract

How to identify protein complex is an important and challenging task in proteomics. It would make great contribution to our knowledge of molecular mechanism in cell life activities. However, the inherent organization and dynamic characteristic of cell system have rarely been incorporated into the existing algorithms for detecting protein complexes because of the limitation of protein-protein interaction (PPI) data produced by high throughput techniques. The availability of time course gene expression profile enables us to uncover the dynamics of molecular networks and improve the detection of protein complexes. In order to achieve this goal, this paper proposes a novel algorithm DCA (Dynamic Core-Attachment). It detects protein-complex core comprising of continually expressed and highly connected proteins in dynamic PPI network, and then the protein complex is formed by including the attachments with high adhesion into the core. The integration of core-attachment feature into the dynamic PPI network is responsible for the superiority of our algorithm. DCA has been applied on two different yeast dynamic PPI networks and the experimental results show that it performs significantly better than the state-of-the-art techniques in terms of prediction accuracy, hF-measure and statistical significance in biology. In addition, the identified complexes with strong biological significance provide potential candidate complexes for biologists to validate.

Indexed as

AlgorithmsProtein Interaction MapsGene Regulatory NetworksMultiprotein ComplexesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsMultiprotein ComplexesSaccharomyces cerevisiae Proteins

Identifiers

PMID29045465
PMCPMC5646790
OpenAlexW2766214346

What OpenQuestion 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 OpenQuestion graph.