Evidence map›Paper›PMID 34077417›Full record

ArticlePLoS computational biology2021

Unsupervised logic-based mechanism inference for network-driven biological processes.

Martina Prugger, Lukas Einkemmer, Samantha P Beik, Perry T Wasdin, Leonard A Harris, Carlos F Lopez

Abstract read
In one paragraph

Article in PLoS computational biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

6 authors.

Martina PruggerDepartment of Biochemistry, University of Innsbruck, Innsbruck, Austria.ORCID 0000-0001-6083-1090
Lukas EinkemmerDepartment of Mathematics, University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-8798-2304
Samantha P BeikDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.ORCID 0000-0002-9546-1656
Perry T WasdinDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.ORCID 0000-0001-7351-2048
Leonard A HarrisDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.ORCID 0000-0003-2112-6940
Carlos F LopezDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.ORCID 0000-0003-3668-7468

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Vanderbilt Biomedical Informatics Training ProgramT15LM007450 · NLM · VANDERBILT UNIVERSITY · PI Jessica S. Ancker, Bradley A. Malin · 2002 to 2026
$19.7M
Single-Cell Biology and Data Analysis Shared Resource (SCB-DA SR)U54CA217450 · NCI · VANDERBILT UNIVERSITY · PI WEAVER, ALISSA M · 2018 to 2022
$8.5M
Medical Scientist Training ProgramT32GM152284 · NIGMS · VANDERBILT UNIVERSITY · PI Christopher S. Williams · 2024 to 2026
$4.8M
Phenotype Transitions in Small Cell Lung CancerU01CA215845 · NCI · VANDERBILT UNIVERSITY · PI LOPEZ, CARLOS FEDERICO, QUARANTA, VITO · 2017 to 2021
$2.8M
Uncovering the molecular networks underlying non-genetic heterogeneity in cancer cell populationsK22CA237857 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI HARRIS, LEONARD ALFREDO L. · 2020 to 2022
$563k
Systems-level mechanisms of small cell lung cancer dynamicsF30CA247078 · NCI · VANDERBILT UNIVERSITY · PI BEIK, SAMANTHA · 2020 to 2023
$144k
NCI NIH HHS F30 CA247078NCI NIH HHS K22 CA237857NCI NIH HHS U01 CA215845NCI NIH HHS U54 CA217450NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32 GM152284NLM NIH HHS T15 LM007450
6 · The paper itself

Abstract

Modern analytical techniques enable researchers to collect data about cellular states, before and after perturbations. These states can be characterized using analytical techniques, but the inference of regulatory interactions that explain and predict changes in these states remains a challenge. Here we present a generalizable, unsupervised approach to generate parameter-free, logic-based models of cellular processes, described by multiple discrete states. Our algorithm employs a Hamming-distance based approach to formulate, test, and identify optimized logic rules that link two states. Our approach comprises two steps. First, a model with no prior knowledge except for the mapping between initial and attractor states is built. We then employ biological constraints to improve model fidelity. Our algorithm automatically recovers the relevant dynamics for the explored models and recapitulates key aspects of the biochemical species concentration dynamics in the original model. We present the advantages and limitations of our work and discuss how our approach could be used to infer logic-based mechanisms of signaling, gene-regulatory, or other input-output processes describable by the Boolean formalism.

Indexed as

Gene Regulatory NetworksLogicModels, BiologicalSignal TransductionAlgorithmsEnzymesEpithelial-Mesenchymal TransitionHumansNeoplasm MetastasisNeoplasmsSubstrate SpecificityEnzymes

Identifiers

PMID34077417
PMCPMC8202945

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.