Evidence map›Paper›PMID 30256780›Full record

ArticlePLoS computational biology2018

An information theoretic treatment of sequence-to-expression modeling.

Farzaneh Khajouei, Saurabh Sinha

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2018. 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
0.4field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Global shape of Toll activation is determined byProceedings of the National Academy of Sciences of the United States of America · 2020
    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

2 authors at 1 institution in 1 country.

Farzaneh KhajoueiDepartment of Computer Science, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.ORCID 0000-0002-0148-9122
Saurabh SinhaDepartment of Computer Science, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.ORCID 0000-0001-6033-7746
University of Illinois Urbana-Champaign · US

Funding

Quantitative Modeling of Sequence-to-Expression RelationshipR01GM114341 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI SINHA, SAURABH · 2015 to 2018
$1.0M
NIGMS NIH HHS R01 GM114341
6 · The paper itself

Abstract

Studying a gene's regulatory mechanisms is a tedious process that involves identification of candidate regulators by transcription factor (TF) knockout or over-expression experiments, delineation of enhancers by reporter assays, and demonstration of direct TF influence by site mutagenesis, among other approaches. Such experiments are often chosen based on the biologist's intuition, from several testable hypotheses. We pursue the goal of making this process systematic by using ideas from information theory to reason about experiments in gene regulation, in the hope of ultimately enabling rigorous experiment design strategies. For this, we make use of a state-of-the-art mathematical model of gene expression, which provides a way to formalize our current knowledge of cis- as well as trans- regulatory mechanisms of a gene. Ambiguities in such knowledge can be expressed as uncertainties in the model, which we capture formally by building an ensemble of plausible models that fit the existing data and defining a probability distribution over the ensemble. We then characterize the impact of a new experiment on our understanding of the gene's regulation based on how the ensemble of plausible models and its probability distribution changes when challenged with results from that experiment. This allows us to assess the 'value' of the experiment retroactively as the reduction in entropy of the distribution (information gain) resulting from the experiment's results. We fully formalize this novel approach to reasoning about gene regulation experiments and use it to evaluate a variety of perturbation experiments on two developmental genes of D. melanogaster. We also provide objective and 'biologist-friendly' descriptions of the information gained from each such experiment. The rigorously defined information theoretic approaches presented here can be used in the future to formulate systematic strategies for experiment design pertaining to studies of gene regulatory mechanisms.

Indexed as

AnimalsBinding SitesComputational BiologyComputer SimulationDrosophila melanogasterEnhancer Elements, GeneticGene Expression ProfilingGene Expression RegulationInformation TheoryModels, BiologicalModels, GeneticMutagenesis, Site-DirectedNormal DistributionProbabilityRegulatory Sequences, Nucleic AcidTranscription FactorsTranscription Factors

Identifiers

PMID30256780
PMCPMC6175532
OpenAlexW2949388760

What OpenQuestion 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 OpenQuestion graph.