%% This code runs based on the previously published
%% paper: http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1003787
%% and code: https://senselab.med.yale.edu/modeldb/showModel.cshtml?model=155565
%% note that all files in lib essentially stayed the same. So if you want to run a bigger sheet, please see previous code for the generation of the connectivity matrix.
%% contact yujiang.wang@ncl.ac.uk for more details
clear all
close all
addpath('lib')
%load('Conns_n150.mat') I recommend generating the connectivity matrix once
%and saving it and loading it in future...
tic;
n=150;
%calculate Connectivity Matrix for Py->Py
CeLoc=GaussianLocConnFunc(n,@distTorus,5);%r_loc=500 micrometre, hence the standard deviation of the gaussian is 250 micrometre, which corresponds to 5 units.
CeLoc(CeLoc>0)=1;
%calculate Connectivity Matrix for Py->In
CeLocI=GaussianLocConnFunc(n,@distTorus,5);%r_loc=500 micrometer
CeLocI(CeLocI>0)=1;
toc;
%remote conn
tic;
nOut=round(mean(sum(CeLoc,1))*4/6);%number of outgoing connections per mini column
%patchSize*numPatches should be > nOut!!!
remRad=75;%3750 micrometers
nM=10;
patchSize=round(5^2*3.14/2);
numPatches=6;
nOverlap=3;
CeRem=ConnPatchyRemOverlap(n,nM,patchSize,numPatches,remRad,nOut,nOverlap,@distTorus,@makeCellClusterToroidal);
toc;
%% parameters
n=150;
tinterp=1;
parameters=getParam(n,CeRem,CeLoc,CeLocI);
P=-1.5;
parameters.PyInput=P*(ones(n^2,1));
%% prescan
%prescan===============================
tend=1.5;
T=0:parameters.h*tinterp:tend;%for plotting
nIt=(tend)/parameters.h+1;
tic
%using all 0 initial condition for Py
initCond=zeros(2*n^2,1);
parameters.NValue=getNoise(nIt,n);
Y=runSheet(initCond,parameters);
bgInitc=Y(end,:);
toc
%% real run
parameters=getParam(n,CeRem,CeLoc,CeLocI);
parameters.tauPy=1.5*1*ones(n^2,1)/25;%time scale of the populations
parameters.tauInh=1.5*0.5*ones(n^2,1)/25;
tend=15;
T=0:parameters.h*tinterp:tend;%for plotting
nIt=(tend)/parameters.h+1;
%!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
ClusterNum=1; %change this number to change the number of subclusters
% !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
PercentHetP=0.05;
parameters.PyInput=P*(ones(n^2,nIt));
CellLocVAll=[];
CellLocAll=zeros(n,n);
Pt=1;
for cn=1:ClusterNum
[CellLoc,CellLocV] = makeCellCluster(1,PercentHetP/ClusterNum,n);%to scan: clustering coeff and percent of bad cells
CellLocVAll=[CellLocVAll, CellLocV];
CellLocAll=CellLocAll+CellLoc;
r=1;
Ramp=[P*ones(1,1000), P:abs((P-Pt))/(1500+r):Pt, Pt*ones(1,5000-r)];
%
parameters.PyInput(CellLocV,:)=repmat(Ramp,length(CellLocV),1);
end
CellLocVAll=unique(CellLocVAll);
%%
%real runs===============================
%using initial condition all 1
tic
initCond=bgInitc;
parameters.NValue=getNoise(nIt,n);
Y=runSheetPRamp(initCond,parameters);
toc
%%
Py=Y(1:tinterp:end,1:n^2);
Inh=Y(1:tinterp:end,n^2+1:end);
SCInput=parameters.NValue(:,1:tinterp:end);
PyInput=parameters.PyInput(:,1:tinterp:end);
LFP=parameters.Py2Py*double(Py') - parameters.Inh2Py*double(Inh') + 0.1*SCInput;% + PyInput + SCInput;
LFP=single(LFP');
mPy=mean(Py,2);sPy=std(Py,0,2);
mLFP=mean(LFP,2);
[mMacroCol,mMacroColLFP]=meanMacroCol(n,10,Py,LFP);
%% plot
load('MayColourMap')
figure(1)
plot(T,mLFP)
title('Raw model output LFP')
samplingF=1/T(2);
filtmLFP=FilterEEG(mLFP, 1, samplingF, 'high', 3);
figure(2)
plot(T,filtmLFP)
title('Filtered model output LFP - with DC shift')
figure(5)
TPts=[1501:200:1501+5*200];
for k=1:length(TPts)
subplot(1,length(TPts),k)
imagesc(reshape(Py(TPts(k),:),n,n) )
%colormap(mycmap)
caxis([0 0.5])
title(sprintf('T=%g',T(TPts(k))))
end