Evidence map›Paper›PMID 31904818›Full record

ArticleBioinformatics (Oxford, England)2020

LiPLike: towards gene regulatory network predictions of high certainty.

Rasmus Magnusson, Mika Gustafsson

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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  5. Article
  6. Review
  7. Article
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  9. Article
  10. Journal of biosciences · 2022
    Review
  11. Article
  12. Computational biology approaches for mapping transcriptional regulatory networks.Computational and structural biotechnology journal · 2021
    Review
  13. 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

2 authors.

Rasmus MagnussonDepartment of Physics, Chemistry and Biology, Linköping University, Linköping 581 83, Sweden.
Mika GustafssonDepartment of Physics, Chemistry and Biology, Linköping University, Linköping 581 83, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationHigh correlation in expression between regulatory elements is a persistent obstacle for the reverse-engineering of gene regulatory networks. If two potential regulators have matching expression patterns, it becomes challenging to differentiate between them, thus increasing the risk of false positive identifications.

resultsTo allow for gene regulation predictions of high confidence, we propose a novel method, the Linear Profile Likelihood (LiPLike), that assumes a regression model and iteratively searches for interactions that cannot be replaced by a linear combination of other predictors. To compare the performance of LiPLike with other available inference methods, we benchmarked LiPLike using three independent datasets from the Dialogue on Reverse Engineering Assessment and Methods 5 (DREAM5) network inference challenge. We found that LiPLike could be used to stratify predictions of other inference tools, and when applied to the predictions of DREAM5 participants, we observed an average improvement in accuracy of >140% compared to individual methods. Furthermore, LiPLike was able to independently predict networks better than all DREAM5 participants when applied to biological data. When predicting the Escherichia coli network, LiPLike had an accuracy of 0.38 for the top-ranked 100 interactions, whereas the corresponding DREAM5 consensus model yielded an accuracy of 0.11. AVAILABILITY AND IMPLEMENTATION: We made LiPLike available to the community as a Python toolbox, available at https://gitlab.com/Gustafsson-lab/liplike. We believe that LiPLike will be used for high confidence predictions in studies where individual model interactions are of high importance, and to remove false positive predictions made by other state-of-the-art gene-gene regulation prediction tools. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsGene Regulatory NetworksBenchmarkingEscherichia coliGene Expression RegulationHumans

Identifiers

PMID31904818
PMCPMC7178405

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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.