Evidence map›Paper›PMID 31510694›Full record

ArticleBioinformatics (Oxford, England)2019

Reconstructing signaling pathways using regular language constrained paths.

Mitchell J Wagner, Aditya Pratapa, T M Murali

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. 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
–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

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.

  1. Functional characterization of co-phosphorylation networks.Bioinformatics (Oxford, England) · 2022
    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

3 authors.

Mitchell J WagnerDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.
Aditya PratapaDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.
T M MuraliDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.

Funding

Integrating Top-Down and Bottom-Up Models in Systems Biology with Application toR01GM095955 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI MURALI, T M · 2011 to 2015
$2.0M
NIGMS NIH HHS R01 GM095955
6 · The paper itself

Abstract

motivationHigh-quality curation of the proteins and interactions in signaling pathways is slow and painstaking. As a result, many experimentally detected interactions are not annotated to any pathways. A natural question that arises is whether or not it is possible to automatically leverage existing pathway annotations to identify new interactions for inclusion in a given pathway.

resultsWe present RegLinker, an algorithm that achieves this purpose by computing multiple short paths from pathway receptors to transcription factors within a background interaction network. The key idea underlying RegLinker is the use of regular language constraints to control the number of non-pathway interactions that are present in the computed paths. We systematically evaluate RegLinker and five alternative approaches against a comprehensive set of 15 signaling pathways and demonstrate that RegLinker recovers withheld pathway proteins and interactions with the best precision and recall. We used RegLinker to propose new extensions to the pathways. We discuss the literature that supports the inclusion of these proteins in the pathways. These results show the broad potential of automated analysis to attenuate difficulties of traditional manual inquiry. AVAILABILITY AND IMPLEMENTATION: https://github.com/Murali-group/RegLinker. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

LanguageSignal TransductionAlgorithmsPublications

Identifiers

PMID31510694
PMCPMC6612893

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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.