Evidence map›Paper›PMID 29641998›Full record

ArticleCell reports2018

Condition-Specific Modeling of Biophysical Parameters Advances Inference of Regulatory Networks.

Konstantine Tchourine, Christine Vogel, Richard Bonneau

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 42 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Konstantine TchourineCenter for Genomics and Systems Biology, New York University, New York, NY 10003, USA; Biology Department, New York University, New York, NY 10003, USA. Electronic address: kmt331@nyu.edu.
Christine VogelCenter for Genomics and Systems Biology, New York University, New York, NY 10003, USA; Biology Department, New York University, New York, NY 10003, USA. Electronic address: cvogel@nyu.edu.
Richard BonneauCenter for Genomics and Systems Biology, New York University, New York, NY 10003, USA; Biology Department, New York University, New York, NY 10003, USA; Courant Institute of Mathematical Sciences, Computer Science Department, New York University, New York, NY 10003, USA; Center for Data Science, New York University, New York, NY 10003, USA; Flatiron Institute, Center for Computational Biology, Simons Foundation, New York, NY 10010, USA. Electronic address: rbonneau@flatironinstitute.org.
New York University · US

Funding

A network model of the gut host-microbe ecosystem in Inflammatory Bowel DiseaseR01DK103358 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BONNEAU, RICHARD A, LITTMAN, DAN · 2014 to 2018
$3.2M
Robust statistical approaches for decoding protein and mRNA expression regulationR01GM113237 · NIGMS · NEW YORK UNIVERSITY · PI VOGEL, CHRISTINE · 2014 to 2017
$1.5M
NIDDK NIH HHS R01 DK103358NIGMS NIH HHS R01 GM113237
6 · The paper itself

Abstract

Large-scale inference of eukaryotic transcription-regulatory networks remains challenging. One underlying reason is that existing algorithms typically ignore crucial regulatory mechanisms, such as RNA degradation and post-transcriptional processing. Here, we describe InfereCLaDR, which incorporates such elements and advances prediction in Saccharomyces cerevisiae. First, InfereCLaDR employs a high-quality Gold Standard dataset that we use separately as prior information and for model validation. Second, InfereCLaDR explicitly models transcription factor activity and RNA half-lives. Third, it introduces expression subspaces to derive condition-responsive regulatory networks for every gene. InfereCLaDR's final network is validated by known data and trends and results in multiple insights. For example, it predicts long half-lives for transcripts of the nucleic acid metabolism genes and members of the cytosolic chaperonin complex as targets of the proteasome regulator Rpn4p. InfereCLaDR demonstrates that more biophysically realistic modeling of regulatory networks advances prediction accuracy both in eukaryotes and prokaryotes.

Indexed as

AlgorithmsGene Regulatory NetworksBacillus subtilisDatabases, GeneticHalf-LifeRNARNA StabilitySaccharomyces cerevisiaeTranscription FactorsRNATranscription Factorsbiophysical modelinggene regulatory networksmachine learningnetwork inferencenetwork remodelingRNA degradation ratesRNA stabilitysaccharomyces cerevisiaesystems biologytranscriptional regulatory networks

Identifiers

PMID29641998
PMCPMC5987223
OpenAlexW2798124328

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.