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Modeling the influences of non-local connectomic projections on geometrically constrained cortical dynamics.

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3 matches between paragraphs of the paper and lines of its authors' code, computed by the harvester (lexical-v1). Click a colored paragraph or line to see its counterpart.

The 3 matches · 1 of them tie a paragraph to a whole file, not to given lines: a weak match, whose lines are not tinted
  1. [1] § Materials and methods › Model implementation ↔ Model/run_absorbing.m, lines 1–48 · score 0.53 · delta impulse, connectivity strength, coupling, traveling, widths, stimulus
  2. [2] § Materials and methods › Model implementation ↔ Model/run_bold_absorbing.m, the whole file · a weak match · score 0.53 · delta impulse, connectivity strength, coupling, traveling, widths, stimulus
  3. [3] § Results › Influence of a complex network of FNPs on cortical dynamics ↔ Experiments/fig7_connectome_nonrandom.m, lines 861–944 · score 0.52 · nearest hub, sampled stimulus positions, rich club, random connectomes, fits, Scatter

Paper

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The authors' code

MATLAB · 190 lines · 6.6 KB · GPL-3.0 · 1 match

  1. function ts = run_absorbing(topology,homparam,hetparam,stim)
  2. % RUN with ZERO TRIVIAL CONDITIONS: phi(r,0) = phi_t(r,0) = 0;
  3. % Absorbing boundary conditions - by adding absorbing layer over Omega
  4. % Layer has width L/2, and has effective gain ranging from nu0 to 0
  5. % Takes in input of model parameters, timesteps and lengthsteps.
  6. % Returns timeseries at each point.
  7. % List of step-size inputs (topology)
  8. % T: time domain [0, T]
  9. % L: space domain [0, L] x [0, L]
  10. % Nt: number of timesteps
  11. % Nx: number of grid points
  12. % List of homogeneous model parameters inputs (homparam)
  13. % gamma: timescale/decay - check that gamma > 0
  14. % r: characteristic axonal length
  15. % check r > 0 && r*gamma < dx/dt (stability)
  16. % nu0: dissipative rate
  17. % check that 0 <= nu0 < 1
  18. % List of heterogeneous model parameters (hetparam)
  19. % G: global coupling parameter
  20. % check G > 0
  21. % m: number of unidirectional pipe
  22. % check m > 0
  23. % cj = c1,..,cm: connectivity strength of jth pipe
  24. % check cj > 0
  25. % tauj = tau1,...,taum: travel time of jth current (as multiples of dt)
  26. % check tauj < |Rji-Rjf|/(r*gamma)
  27. % Rji = R1i,...,Rmi: regions at which pipe starts
  28. % check Rjis are in 1:N1x1:N2
  29. % Rjf = R1f,...,Rmf: regions at which pipe ends
  30. % check Rjfs are in 1:N1x1:N2
  31. % check mutually exclusive: does not exist any j1,j2 with
  32. % overlapping Rji and overlapping Rjf
  33. % List of stimulation inputs (stim)
  34. % stimnum: number of times of stimulation
  35. % stimtk = stimt1,...,stimtn = times of stimulation - check less than Nt
  36. % stimIk = stimI1,...,stimIn = stimulation intensity
  37. % stimRk = stimR1,...,stimRn = stimulation positions
  38. % sigma = [sigma_x, sigma_t] = Gaussian approximation of delta impulse
  39. % Outputs
  40. % ts: Nx x Ny x Nt timeseries array
  41. dx = topology.L / topology.Nx;
  42. dt = topology.T / topology.Nt;
  43. if (homparam.r * homparam.gamma * sqrt(2) > dx / dt)
  44. error('Error, Unstable choice of dx and dt')
  45. end
  46. % Find dimensions of outer square
  47. % Find least number of grid points needed to create of
  48. Nxabs = round(topology.L/2 / dx);
  49. Nxtot = topology.Nx + 2*Nxabs;
  50. % Initiate output timeseries array
  51. ts = zeros(topology.Nx, topology.Nx, topology.Nt);
  52. % Initiate temporary recursive timeseries array
  53. % Need at least tauj previous timesteps for convolution
  54. % and at least 1 previous timestep for wave equation
  55. % Therefore we track 1 + max(tau, 1) timesteps for each iteration
  56. if hetparam.m > 0
  57. phi = zeros(Nxtot, Nxtot, 1 + max([ceil(hetparam.tau/dt), 1]));
  58. else
  59. phi = zeros(Nxtot, Nxtot, 2);
  60. end
  61. if hetparam.m > 0
  62. % Change hetparam.Ri and hetparam.Rf to 3D array if they are 2D
  63. Ra = zeros(topology.Nx, topology.Nx, hetparam.m);
  64. Rb = zeros(topology.Nx, topology.Nx, hetparam.m);
  65. for k = 1:hetparam.m
  66. a_x = hetparam.a(1, k); a_y = hetparam.a(2, k);
  67. for i = 1:topology.Nx
  68. for j = 1:topology.Nx
  69. distx = abs(i*dx - a_x);
  70. disty = abs(j*dx - a_y);
  71. Ra(i, j, k) = exp(-0.5*(distx^2 + disty^2) / (hetparam.sigmaeps)^2);
  72. end
  73. end
  74. end
  75. for k = 1:hetparam.m
  76. b_x = hetparam.b(1, k); b_y = hetparam.b(2, k);
  77. for i = 1:topology.Nx
  78. for j = 1:topology.Nx
  79. distx = abs(i*dx - b_x);
  80. disty = abs(j*dx - b_y);
  81. Rb(i, j, k) = exp(-0.5*(distx^2 + disty^2) / (hetparam.sigmaeps)^2);
  82. end
  83. end
  84. end
  85. for k = 1:hetparam.m
  86. Ra(:, :, k) = Ra(:, :, k)/sum(Ra(:, :, k),'all');
  87. Rb(:, :, k) = Rb(:, :, k)/sum(Rb(:, :, k),'all');
  88. end
  89. hetparam.Ra = Ra;
  90. hetparam.Rb = Rb;
  91. % Turn hetparam.c into c / dx^2, so I dont have to keep multiplying
  92. hetparam.c = hetparam.c / dx^2;
  93. end
  94. % Create array of stimulation inputs by space
  95. stimulationinputspace = zeros(topology.Nx, topology.Nx, stim.stimnum);
  96. for n = 1:stim.stimnum
  97. i0 = stim.stimR(1, n) / dx; j0 = stim.stimR(2, n) / dx;
  98. for i = 1:topology.Nx
  99. for j = 1:topology.Nx
  100. distx = abs(i - i0);
  101. disty = abs(j - j0);
  102. stimulationinputspace(i, j, n) = exp(-0.5*(distx^2 + disty^2) * (dx^2) / (stim.sigma(1)^2));
  103. end
  104. end
  105. end
  106. stimulationinputspace = stimulationinputspace * 1/(2*pi * stim.sigma(1)^2);
  107. % Create array of stimulation inputs by time
  108. stimulationinputtime = zeros(topology.Nt, stim.stimnum);
  109. for k = 1:stim.stimnum
  110. t0 = stim.stimt(k) / dt;
  111. for n = 1:topology.Nt
  112. distt = abs((n - 1) - t0);
  113. stimulationinputtime(n, k) = exp(-0.5 *(distt^2) * (dt^2) / (stim.sigma(2)^2));
  114. end
  115. end
  116. stimulationinputtime = stimulationinputtime * 1/(sqrt(2*pi) * stim.sigma(2));
  117. % Normalise stimulationinputspace and stimulationinputtime so that weights
  118. % add to 1/dx^2 and 1/dt respectively
  119. for k = 1:stim.stimnum
  120. stimulationinputspace(:, :, k) = (1/dx^2) * ...
  121. stimulationinputspace(:, :, k) / sum(stimulationinputspace(:, :, k), "all");
  122. stimulationinputtime(:, k) = (1/dt) * ...
  123. stimulationinputtime(:, k) / sum(stimulationinputtime(:, k), 'all');
  124. end
  125. % Add absorbing layer
  126. nu0_array = zeros(Nxtot, Nxtot);
  127. for i = 1:Nxabs
  128. nu0_array(i : (Nxtot + 1 - i), i : (Nxtot + 1 - i)) = (i - 1) * homparam.nu0 / Nxabs;
  129. end
  130. nu0_array(Nxabs + (1 : topology.Nx), Nxabs + (1 : topology.Nx)) = homparam.nu0;
  131. for count = 1:topology.Nt
  132. % Calculate input for wave equation: nu0*phi + r^2*nabla^2(phi) + C(phi) + P
  133. recurrentinput = nu0_array .* phi(:, :, end);
  134. laplacianinput = (homparam.r / dx)^2 * Laplacian_2D(phi(:, :, end));
  135. if hetparam.m > 0
  136. convolutioninput = Convolution(hetparam, phi(Nxabs + (1:topology.Nx), Nxabs + (1:topology.Nx), :), dt);
  137. else
  138. convolutioninput = 0;
  139. end
  140. stimulationinput = zeros(topology.Nx, topology.Nx);
  141. for k = 1:stim.stimnum
  142. stimulationinput = stimulationinput + ...
  143. stim.stimI(k) * stimulationinputspace(:, :, k) * stimulationinputtime(count, k);
  144. end
  145. input = zeros(Nxtot, Nxtot);
  146. input(Nxabs + (1:topology.Nx), Nxabs + (1:topology.Nx)) = convolutioninput + stimulationinput;
  147. input = input + recurrentinput + laplacianinput;
  148. if count == 1
  149. % Initial velocity conditions imply that phi_1 = phi_{-1}, hence...
  150. phinew = 0.5 * input * (homparam.gamma * dt)^2;
  151. else
  152. phinew = wave_eq_2D(phi, input, homparam.gamma * dt);
  153. end
  154. phi(:, :, 1:end-1) = phi(:, :, 2:end);
  155. phi(:, :, end) = phinew;
  156. ts(:, :, count) = phinew(Nxabs + (1:topology.Nx), Nxabs + (1:topology.Nx));;
  157. end
  158. end

run_absorbing.m at commit 2c6fde1, under GPL-3.0 · at the source

Overview

Authors: Rishikesan Maran1,2, Eli J Müller1,2,3, Ben D Fulcher1,2
ORCID iDs: Ben D Fulcher
  1. School of Physics, The University of Sydney, Sydney, New South Wales, Australia
  2. Centre for Complex Systems, The University of Sydney, Sydney, New South Wales, Australia
  3. School of Medical Sciences, The University of Sydney, Sydney, New South Wales, Australia
Institutions: The University of Sydney (Australia)
Journal: PLoS computational biology, volume 22, issue 8, article e1014673
Dates: received 20 March 2026; accepted 5 August 2026; published online 26 August 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1371/journal.pcbi.1014673 · PMID 42647573 · PMCID PMC13552967 · OpenAlex W4414684716
Open access: gold, a free copy (OpenAlex)
Status: code verified
Categories: human (organism), computational (subfield)
Methods: Machine learning
MeSH: Cerebral Cortex*, Connectome*, Models, Neurological*, Nerve Net*, Animals, Computational Biology, Computer Simulation, Humans (* major topic)
Topic: Functional Brain Connectivity Studies (Cognitive Neuroscience, Neuroscience), according to OpenAlex
Funding: Australian Research Council (FT240100418, DP240101295, DE250100540); Australian Government Research Training Program; Australian Government Research Training Program (RTP) scholarship
Citations: not cited yet (Europe PMC); 109 references in the paper

Abstract

The function and dynamics of the cortex are fundamentally shaped by the specific wiring configurations of its constituent axonal fibers, also known as the connectome. However, many dynamical properties of macroscale cortical activity are well captured by instead describing the activity as propagating waves across the cortical surface, constrained only by the surface’s two-dimensional geometry. It thus remains an open question why the local geometry of the cortex can successfully capture macroscale cortical dynamics, despite neglecting the specificity of Fast-conducting, Non-local Projections (FNPs) which are known to mediate the rapid and non-local propagation of activity between remote neural populations. Here we address this question by conducting a range of investigations using a mathematical model of macroscale cortical activity, in which cortical populations interact both by a continuous sheet and by an additional set of FNPs wired independently of the sheet’s geometry. By simulating the model across a range of external inputs, timescales, and idealized connectome topologies, we demonstrate that the addition of FNPs strongly shape the model dynamics of rapid, stimulus-evoked responses on fine millisecond timescales, but contribute relatively little to slower, spontaneous fluctuations over longer order-of-seconds timescales, which increasingly resemble geometrically constrained dynamics without FNPs. Our results suggest that the discrepant views regarding the relative contributions of local (geometric) and non-local (connectomic) cortico-cortical interactions are context-dependent: While FNPs specified by the connectome are needed to capture rapid communication between specific distant populations (as per the rapid processing of sensory inputs), they play a relatively minor role in shaping slower spontaneous fluctuations (as per resting-state functional magnetic resonance imaging).

Reproduced under the paper's license (CC BY), from the paper cited above.

Repository

Its files are read in the Code ↔ Paper reader above, with 3 matches between paragraphs and lines of code.

DynamicsAndNeuralSystems/geometricFNPmodel

License: GPL-3.0
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 2c6fde160b2e28e9e4e3ae0283e96940cc39d4f7, 7 June 2026
Languages: MATLAB (26)
Size: 40 files, 26 scripts
Software Heritage: not archived
Found in: “Data Availability”
Holds: README, license file
Not found: CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
28 files

The paper's code and data availability statement is in the Data section.

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  • 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 26 scripts, each with its path and the digest of its content;
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Data

No dataset and no data link were found in the paper.

Data Availability

Code to reproduce results reported here is available at https://github.com/DynamicsAndNeuralSystems/geometricFNPmodel.

Reproduced under the paper's license (CC BY), from the paper cited above.

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Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 3 authors, 8 MeSH terms, 3 funders, 101 references.

Cite

This paper

Maran, R., Müller, E. J., & Fulcher, B. D. (2026). Modeling the influences of non-local connectomic projections on geometrically constrained cortical dynamics. PLoS computational biology, 22(8), e1014673. https://doi.org/10.1371/journal.pcbi.1014673

BibTeX

@article{maran2026modeling,
author = {Maran, Rishikesan and Müller, Eli J and Fulcher, Ben D},
title = {{Modeling the influences of non-local connectomic projections on geometrically constrained cortical dynamics}},
journal = {PLoS computational biology},
year = {2026},
month = aug,
volume = {22},
number = {8},
pages = {e1014673},
publisher = {PLOS},
issn = {1553-734X},
doi = {10.1371/journal.pcbi.1014673},
url = {https://doi.org/10.1371/journal.pcbi.1014673},
pmid = {42647573},
pmcid = {PMC13552967}
}

RIS

TY - JOUR
AU - Maran, Rishikesan
AU - Müller, Eli J
AU - Fulcher, Ben D
TI - Modeling the influences of non-local connectomic projections on geometrically constrained cortical dynamics
T2 - PLoS computational biology
J2 - PLoS Comput Biol
PY - 2026
DA - 2026/08/26
VL - 22
IS - 8
SP - e1014673
SN - 1553-734X
PB - PLOS
DO - 10.1371/journal.pcbi.1014673
UR - https://doi.org/10.1371/journal.pcbi.1014673
LA - en
ER -

CSL-JSON

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