Evidence map›Paper›PMID 27716036›Full record

ArticleBMC bioinformatics2016

Identification of large disjoint motifs in biological networks.

Rasha Elhesha, Tamer Kahveci

Abstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Compression-based inference of network motif sets.PLoS computational biology · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Counting motifs in dynamic networks.BMC systems biology · 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

2 authors.

Rasha ElheshaCISE Department, University of Florida, 432 Newell Dr, Gainesville, Florida, 32611, USA. relhesha@cise.ufl.edu.
Tamer KahveciCISE Department, University of Florida, 432 Newell Dr, Gainesville, Florida, 32611, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiological networks provide great potential to understand how cells function. Network motifs, frequent topological patterns, are key structures through which biological networks operate. Finding motifs in biological networks remains to be computationally challenging task as the size of the motif and the underlying network grow. Often, different copies of a given motif topology in a network share nodes or edges. Counting such overlapping copies introduces significant problems in motif identification.

resultsIn this paper, we develop a scalable algorithm for finding network motifs. Unlike most of the existing studies, our algorithm counts independent copies of each motif topology. We introduce a set of small patterns and prove that we can construct any larger pattern by joining those patterns iteratively. By iteratively joining already identified motifs with those patterns, our algorithm avoids (i) constructing topologies which do not exist in the target network (ii) repeatedly counting the frequency of the motifs generated in subsequent iterations. Our experiments on real and synthetic networks demonstrate that our method is significantly faster and more accurate than the existing methods including SUBDUE and FSG.

conclusionsWe conclude that our method for finding network motifs is scalable and computationally feasible for large motif sizes and a broad range of networks with different sizes and densities. We proved that any motif with four or more edges can be constructed as a join of the small patterns.

Indexed as

AlgorithmsGene Regulatory NetworksPattern Recognition, AutomatedAmino Acid MotifsComputational BiologyHerpesvirus 8, HumanHumansProtein Interaction MappingViral ProteinsViral ProteinsBiological networksMotif discoveryOverlap graphSubgraph isomorphism

Identifiers

PMID27716036
PMCPMC5053092

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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.