Evidence map›Paper›PMID 32676097›Full record

ArticleFrontiers in genetics2020

DPCT: A Dynamic Method for Detecting Protein Complexes From TAP-Aware Weighted PPI Network.

Ali SabziNezhad, Saeed Jalili

Abstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. 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

2 authors.

Ali SabziNezhadComputer Engineering Department, Tarbiat Modares University, Tehran, Iran.
Saeed JaliliComputer Engineering Department, Tarbiat Modares University, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detecting protein complexes from the Protein-Protein interaction network (PPI) is the essence of discovering the rules of the cellular world. There is a large amount of PPI data available, generated from high throughput experimental data. The enormous size of the data persuaded us to use computational methods instead of experimental methods to detect protein complexes. In past years, many researchers presented their algorithms to detect protein complexes. Most of the presented algorithms use current static PPI networks. New researches proved the dynamicity of cellular systems, and so, the PPI is not static over time. In this paper, we introduce DPCT to detect protein complexes from dynamic PPI networks. In the proposed method, TAP and GO data are used to make a weighted PPI network and to reduce the noise of PPI. Gene expression data are also used to make dynamic subnetworks from PPI. A memetic algorithm is used to bicluster gene expression data and to create a dynamic subnetwork for each bicluster. Experimental results show that DPCT can detect protein complexes with better correctness than state-of-the-art detection algorithms. The source code and datasets of DPCT used can be found at https://github.com/alisn72/DPCT.

Indexed as

biclusteringmemetic algorithmPPI networkprotein complexTAP data

Identifiers

PMID32676097
PMCPMC7333736

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.