Evidence map›Paper›PMID 34707916›Full record

ArticleProceedings of the ... AAAI Conference on Artificial Intelligence. AAAI Conference on Artificial Intelligence2021

Gene regulatory network inference as relaxed graph matching.

Deborah Weighill, Marouen Ben Guebila, Camila Lopes-Ramos, Kimberly Glass, John Quackenbush, John Platig, Rebekka Burkholz

Abstract read
In one paragraph

Article in Proceedings of the ... AAAI Conference on Artificial Intelligence. AAAI Conference on Artificial Intelligence, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  10. Network-based drug repurposing for schizophrenia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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  18. Cascade Size Distributions: Why They Matter and How to Compute Them Efficiently.Proceedings of the ... AAAI Conference on Artificial Intelligence. AAAI Conference on Artificial Intelligence · 2021
    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

7 authors.

Deborah WeighillDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115.
Marouen Ben GuebilaDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115.
Camila Lopes-RamosDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115.
Kimberly GlassDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115.
John QuackenbushDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115.
John PlatigChanning Division of Network Medicine, Brigham and Women's Hospital.
Rebekka BurkholzDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115.

Funding

Unraveling the Complexities of Risk and Mechanism in CancerR35CA220523 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI QUACKENBUSH, JOHN · 2018 to 2024
$6.0M
Using Integrative Networks to Explore Heterogeneous Phenotypes in COPDK25HL133599 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI GLASS, KIMBERLY RENEE · 2016 to 2020
$945k
Context matters: Network modeling of COPD regulatory variants across tissues and exposuresK25HL140186 · NHLBI · UNIVERSITY OF VIRGINIA · PI PLATIG, JOHN · 2018 to 2022
$926k
NCI NIH HHS R35 CA220523NHLBI NIH HHS K25 HL133599NHLBI NIH HHS K25 HL140186
6 · The paper itself

Abstract

Bipartite network inference is a ubiquitous problem across disciplines. One important example in the field molecular biology is gene regulatory network inference. Gene regulatory networks are an instrumental tool aiding in the discovery of the molecular mechanisms driving diverse diseases, including cancer. However, only noisy observations of the projections of these regulatory networks are typically assayed. In an effort to better estimate regulatory networks from their noisy projections, we formulate a non-convex but analytically tractable optimization problem called OTTER. This problem can be interpreted as relaxed graph matching between the two projections of the bipartite network. OTTER's solutions can be derived explicitly and inspire a spectral algorithm, for which we provide network recovery guarantees. We also provide an alternative approach based on gradient descent that is more robust to noise compared to the spectral algorithm. Interestingly, this gradient descent approach resembles the message passing equations of an established gene regulatory network inference method, PANDA. Using three cancer-related data sets, we show that OTTER outperforms state-of-the-art inference methods in predicting transcription factor binding to gene regulatory regions. To encourage new graph matching applications to this problem, we have made all networks and validation data publicly available.

Identifiers

PMID34707916
PMCPMC8546743

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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.