Evidence map›Paper›PMID 34025035›Full record

ArticleNeurocomputing2020

DNF: A differential network flow method to identify rewiring drivers for gene regulatory networks.

Jiang Xie, Fuzhang Yang, Jiao Wang, Mathew Karikomi, Yiting Yin, Jiamin Sun, Tieqiao Wen, Qing Nie

Abstract read
In one paragraph

Article in Neurocomputing, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

8 authors.

Jiang XieSchool of Computer Engineering and Science, Shanghai University, Shanghai 200444, China.
Fuzhang YangSchool of Computer Engineering and Science, Shanghai University, Shanghai 200444, China.
Jiao WangLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Mathew KarikomiDepartment of Mathematics, Department of Developmental and Cell Biology, University of California, Irvine, CA 92697-3875, USA.
Yiting YinSchool of Computer Engineering and Science, Shanghai University, Shanghai 200444, China.
Jiamin SunSchool of Computer Engineering and Science, Shanghai University, Shanghai 200444, China.
Tieqiao WenLaboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai 200444, China.
Qing NieDepartment of Mathematics, Department of Developmental and Cell Biology, University of California, Irvine, CA 92697-3875, USA.

Funding

Shared Resource Core: Single Cell AnalysisU54CA217378 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI VAN ETTEN, RICHARD A. · 2018 to 2022
$9.7M
Multiscale Models of Wound Cell Plasticity for RegenerationU01AR073159 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI DAI, XING, NIE, QING · 2018 to 2022
$3.5M
NCI NIH HHS U54 CA217378NIAMS NIH HHS U01 AR073159
6 · The paper itself

Abstract

Differential network analysis has become an important approach in identifying driver genes in development and disease. However, most studies capture only local features of the underlying gene-regulatory network topology. These approaches are vulnerable to noise and other changes which mask driver-gene activity. Therefore, methods are urgently needed which can separate the impact of true regulatory elements from stochastic changes and downstream effects. We propose the differential network flow (DNF) method to identify key regulators of progression in development or disease. Given the network representation of consecutive biological states, DNF quantifies the essentiality of each node by differences in the distribution of network flow, which are capable of capturing comprehensive topological differences from local to global feature domains. DNF achieves more accurate driver-gene identification than other state-of-the-art methods when applied to four human datasets from The Cancer Genome Atlas and three single-cell RNA-seq datasets of murine neural and hematopoietic differentiation. Furthermore, we predict key regulators of crosstalk between separate networks underlying both neuronal differentiation and the progression of neurodegenerative disease, among which APP is predicted as a driver gene of neural stem cell differentiation. Our method is a new approach for quantifying the essentiality of genes across networks of different biological states.

Indexed as

differential network analysisinformation entropynetwork flownetwork topologyneuronal differentiation

Identifiers

PMID34025035
PMCPMC8139126

What OpenQuestion holds

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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.