Evidence map›Paper›PMID 25379138›Full record

ReviewComputational and structural biotechnology journal2014

Using biological networks to improve our understanding of infectious diseases.

Nicola J Mulder, Richard O Akinola, Gaston K Mazandu, Holifidy Rapanoel

Open access · goldAbstract readReview
In one paragraph

Review in Computational and structural biotechnology journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Journal of biosciences · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Pairwise Versus Multiple Global Network Alignment.IEEE access : practical innovations, open solutions · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. The effects of shared information on semantic calculations in the gene ontology.Computational and structural biotechnology journal · 2017
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. The post-genomic era of biological network alignment.EURASIP journal on bioinformatics & systems biology · 2015
    Article
  20. Review
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

4 authors at 1 institution in 1 country.

Nicola J MulderComputational Biology Group, Department of Clinical Laboratory Sciences, IDM, University of Cape Town Faculty of Health Sciences, Anzio Road, Observatory, Cape Town, South Africa.
Richard O AkinolaComputational Biology Group, Department of Clinical Laboratory Sciences, IDM, University of Cape Town Faculty of Health Sciences, Anzio Road, Observatory, Cape Town, South Africa.
Gaston K MazanduComputational Biology Group, Department of Clinical Laboratory Sciences, IDM, University of Cape Town Faculty of Health Sciences, Anzio Road, Observatory, Cape Town, South Africa.
Holifidy RapanoelComputational Biology Group, Department of Clinical Laboratory Sciences, IDM, University of Cape Town Faculty of Health Sciences, Anzio Road, Observatory, Cape Town, South Africa.
University of Cape Town · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infectious diseases are the leading cause of death, particularly in developing countries. Although many drugs are available for treating the most common infectious diseases, in many cases the mechanism of action of these drugs or even their targets in the pathogen remain unknown. In addition, the key factors or processes in pathogens that facilitate infection and disease progression are often not well understood. Since proteins do not work in isolation, understanding biological systems requires a better understanding of the interconnectivity between proteins in different pathways and processes, which includes both physical and other functional interactions. Such biological networks can be generated within organisms or between organisms sharing a common environment using experimental data and computational predictions. Though different data sources provide different levels of accuracy, confidence in interactions can be measured using interaction scores. Connections between interacting proteins in biological networks can be represented as graphs and edges, and thus studied using existing algorithms and tools from graph theory. There are many different applications of biological networks, and here we discuss three such applications, specifically applied to the infectious disease tuberculosis, with its causative agent Mycobacterium tuberculosis and host, Homo sapiens. The applications include the use of the networks for function prediction, comparison of networks for evolutionary studies, and the generation and use of host-pathogen interaction networks.

Indexed as

Biological networksEvolutionPathogenProtein–protein interactionTuberculosis

Identifiers

PMID25379138
PMCPMC4212278
OpenAlexW2105851205

What OpenQuestion holds

Textmetadata
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.