Evidence map›Paper›PMID 30389942›Full record

ArticleNature communications2018

An information-theoretic framework for deciphering pleiotropic and noisy biochemical signaling.

Tomasz Jetka, Karol Nienałtowski, Sarah Filippi, Michael P H Stumpf, Michał Komorowski

Abstract read
In one paragraph

Article in Nature communications, 2018. 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

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

13 citing papers in PubMed.

  1. Fundamental limits incorporating logical reasoning into Shannon's information theory.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  4. Quantifying information of intracellular signaling: progress with machine learning.Reports on progress in physics. Physical Society (Great Britain) · 2022
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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

5 authors.

Tomasz JetkaInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warszawa, 02-106, Poland.
Karol NienałtowskiInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warszawa, 02-106, Poland.
Sarah FilippiDepartment of Mathematics and School of Public Health, Imperial College London, London, SW7 2AZ, UK.
Michael P H StumpfMelbourne Integrative Genomics, School of BioSciences and School of Mathematics and Statistics, University of Melbourne, Parkville, 3010, VIC, Australia.ORCID http://orcid.org/0000-0002-3577-1222
Michał KomorowskiInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warszawa, 02-106, Poland. m.komorowski@sysbiosig.org.

Funding

Biotechnology and Biological Sciences Research Council BB/G020434/1Medical Research Council G1002092
6 · The paper itself

Abstract

Many components of signaling pathways are functionally pleiotropic, and signaling responses are marked with substantial cell-to-cell heterogeneity. Therefore, biochemical descriptions of signaling require quantitative support to explain how complex stimuli (inputs) are encoded in distinct activities of pathways effectors (outputs). A unique perspective of information theory cannot be fully utilized due to lack of modeling tools that account for the complexity of biochemical signaling, specifically for multiple inputs and outputs. Here, we develop a modeling framework of information theory that allows for efficient analysis of models with multiple inputs and outputs; accounts for temporal dynamics of signaling; enables analysis of how signals flow through shared network components; and is not restricted by limited variability of responses. The framework allows us to explain how identity and quantity of type I and type III interferon variants could be recognized by cells despite activating the same signaling effectors.

Indexed as

Genetic PleiotropyInformation TheorySignal TransductionInterferon LambdaInterferonsInterferon Type IKineticsModels, BiologicalInterferon LambdaInterferonsInterferon Type I

Identifiers

PMID30389942
PMCPMC6214929

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Registered trials

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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.