Evidence map›Paper›PMID 31736734›Full record

ArticleFrontiers in computational neuroscience2019

Extracting Reproducible Time-Resolved Resting State Networks Using Dynamic Mode Decomposition.

James M Kunert-Graf, Kristian M Eschenburg, David J Galas, J Nathan Kutz, Swati D Rane, Bingni W Brunton

Abstract read
In one paragraph

Article in Frontiers in computational neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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  10. Simplicial and topological descriptions of human brain dynamics.Network neuroscience (Cambridge, Mass.) · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Metastable Resting State Brain Dynamics.Frontiers in computational neuroscience · 2019
    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.

James M Kunert-GrafPacific Northwest Research Institute, Seattle, WA, United States.
Kristian M EschenburgDepartment of Bioengineering, University of Washington, Seattle, WA, United States.
David J GalasPacific Northwest Research Institute, Seattle, WA, United States.
J Nathan KutzDepartment of Applied Math, University of Washington, Seattle, WA, United States.
Swati D RaneDepartment of Radiology, University of Washington, Seattle, WA, United States.
Bingni W BruntonDepartment of Biology, University of Washington, Seattle, WA, United States.

Funding

Cerebrovascular imaging of mild cognitive impairment with suspected non-amyloid pathologyK01AG055669 · NIA · UNIVERSITY OF WASHINGTON · PI RANE LEVENDOVSZKY, SWATI · 2017 to 2021
$616k
NIA NIH HHS K01 AG055669
6 · The paper itself

Abstract

Resting state networks (RSNs) extracted from functional magnetic resonance imaging (fMRI) scans are believed to reflect the intrinsic organization and network structure of brain regions. Most traditional methods for computing RSNs typically assume these functional networks are static throughout the duration of a scan lasting 5-15 min. However, they are known to vary on timescales ranging from seconds to years; in addition, the dynamic properties of RSNs are affected in a wide variety of neurological disorders. Recently, there has been a proliferation of methods for characterizing RSN dynamics, yet it remains a challenge to extract reproducible time-resolved networks. In this paper, we develop a novel method based on dynamic mode decomposition (DMD) to extract networks from short windows of noisy, high-dimensional fMRI data, allowing RSNs from single scans to be resolved robustly at a temporal resolution of seconds. After validating the method on a synthetic dataset, we analyze data from 120 individuals from the Human Connectome Project and show that unsupervised clustering of DMD modes discovers RSNs at both the group (gDMD) and the single subject (sDMD) levels. The gDMD modes closely resemble canonical RSNs. Compared to established methods, sDMD modes capture individualized RSN structure that both better resembles the population RSN and better captures subject-level variation. We further leverage this time-resolved sDMD analysis to infer occupancy and transitions among RSNs with high reproducibility. This automated DMD-based method is a powerful tool to characterize spatial and temporal structures of RSNs in individual subjects.

Indexed as

dynamic mode decomposition (DMD)human connectome project (HCP)individualized networksnetwork dynamicsresting state network (RSN)RS-fMRI

Identifiers

PMID31736734
PMCPMC6834549

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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.