%
% OBS kolla nu så att rand-längderna sätts rätt på de olika compartments
%
% FUNDERING: Antingen förstorar jag alla tert-dend kompartments lika
% och då ska inte varje sub-kompartment få olika storlek, ty det är
% bara en numerisk behandling... har inget med morphologin att göra
% eller så ska jag slumpa alla compartments oberoende av varandra
% för att bryta symmetrin...
%
% Tror i första approx att jag bara förstorar alla tert-dends.
% Generates nCells number of p-files for the FSMorphology
% maxVar = variation, ie 0.10 = 10% (randomized)
% channelsVar = name of channels to vary, in a cell-matrix
% compLenVar = variation of compartment length
function makeFSMorphMOD(cellIdx, maxVar, channelsVar, compLenVar)
path = [pwd '/INDATA/'];
fnMask = 'FSmorph-%d.p';
compParam{1} = 'ELEAK'; compValue(1) = -0.063;
compParam{2} = 'RA'; compValue(2) = 3;
compParam{3} = 'RM'; compValue(3) = 2;
compParam{4} = 'CM'; compValue(4) = 0.007;
compParam{5} = 'EREST_ACT'; compValue(5) = -0.063;
tertChanName = {'AMPA_channel', 'GABA_channel'};
tertChanCondBase = [16, 24];
secChanName = {'AMPA_channel', 'GABA_channel'};
secChanCondBase = [8.65, 13];
primChanName = {'AMPA_channel', 'GABA_channel', 'A_channel_MOD'};
primChanCondBase = [5.333, 8.0, 90];
somaChanName = {'Na_channel_MOD', 'K3132_channel_MOD', 'A_channel_MOD', ...
'K13_channel_MOD', 'AMPA_channel', 'GABA_channel'};
somaChanCondBase = [1149, 582, 333, 1.46, 0.8, 1.2];
somaChanMask = zeros(size(somaChanCondBase));
primChanMask = zeros(size(primChanCondBase));
secChanMask = zeros(size(secChanCondBase));
tertChanMask = zeros(size(tertChanCondBase));
for i=1:length(channelsVar)
somaChanMask = somaChanMask | strcmp(somaChanName, channelsVar{i});
primChanMask = primChanMask | strcmp(primChanName, channelsVar{i});
secChanMask = secChanMask | strcmp(secChanName, channelsVar{i});
tertChanMask = tertChanMask | strcmp(tertChanName, channelsVar{i});
end
% Just a error check...
for i=1:length(channelsVar)
if(sum(strcmp(somaChanName, channelsVar{i})) ...
| sum(strcmp(primChanName, channelsVar{i})) ...
| sum(strcmp(secChanName, channelsVar{i})) ...
| sum(strcmp(tertChanName, channelsVar{i})))
disp(['Varying channel ' channelsVar{i} ' by ' ...
num2str(maxVar*100) '%'])
else
disp(['Warning, no channel ' channelsVar{i} ...
' found, did you spell it right?'])
disp('Type return to continue')
keyboard
end
end
%%%%% Length variation
disp(['Varying length by ' num2str(compLenVar*100) ' %'])
tertLen = 30;
secLen = 37;
primLen = 45;
somaLen = 20;
for iCell = cellIdx %1:nCells
libName = ['cell' num2str(iCell)];
% Varje cell får sin egen slumpade uppsättning
% keyboard
tertChanCond = tertChanCondBase ...
.* (1 + tertChanMask*maxVar.*(1-2*rand(size(tertChanCondBase))));
secChanCond = secChanCondBase ...
.* (1 + secChanMask*maxVar.*(1-2*rand(size(secChanCondBase))));
primChanCond = primChanCondBase ...
.* (1 + primChanMask*maxVar.*(1-2*rand(size(primChanCondBase))));
somaChanCond = somaChanCondBase ...
.* (1 + somaChanMask*maxVar.*(1-2*rand(size(somaChanCondBase))));
tLen = tertLen*(1 + compLenVar*(1-2*rand));
sLen = secLen*(1 + compLenVar*(1-2*rand));
pLen = primLen*(1 + compLenVar*(1-2*rand));
soLen = somaLen*(1 + compLenVar*(1-2*rand));
fn = sprintf(fnMask, iCell);
fid = fopen([path fn], 'w');
fprintf(fid, '*relative\n*cartesian\n*asymmetric\n*lambda_warn\n\n');
for j=1:length(compParam)
fprintf(fid, '*set_compt_param %s %f \n', compParam{j}, compValue(j));
end
%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
%% Creating templates for compartments
compNum{1} = '';
parentName{1} = 'none';
for i=2:8
compNum{i} = num2str(i);
parentName{i} = '.';
end
%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
%% Tertiary dendrites
fprintf(fid, ['\n*start_cell /library/' libName '/tert_dend\n']);
for i=1:8
fprintf(fid, ['\ntert_dend' compNum{i} ' ' parentName{i} ...
' ' num2str(tLen) ' 0 0 0.5 ']);
for j=1:length(tertChanName)
fprintf(fid, '%s %d ', tertChanName{j}, tertChanCond(j));
end
end
fprintf(fid,['\n*makeproto /library/' libName '/tert_dend\n\n']);
%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
%% Secondary dendrites
fprintf(fid, ['*start_cell /library/' libName '/sec_dend\n']);
for i=1:4
fprintf(fid, ['\nsec_dend' compNum{i} ' ' parentName{i} ...
' ' num2str(sLen) ' 0 0 0.75 ']);
for j=1:length(secChanName)
fprintf(fid, '%s %d ', secChanName{j}, secChanCond(j));
end
end
fprintf(fid, ['\n*makeproto /library/' libName '/sec_dend\n\n']);
%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
%% Primary dendrites
fprintf(fid, ['*start_cell /library/' libName '/prim_dend\n']);
for i=1:2
fprintf(fid, ['\nprim_dend' compNum{i} ' ' parentName{i} ...
' ' num2str(pLen) ' 0 0 1 ']);
for j=1:length(primChanName)
fprintf(fid, '%s %d ', primChanName{j}, primChanCond(j));
end
end
fprintf(fid, ['\n*makeproto /library/' libName '/prim_dend\n\n']);
%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
%% Soma
fprintf(fid, '*start_cell\n');
fprintf(fid, ['soma none ' num2str(soLen) ' 0 0 15 ']);
for j=1:length(somaChanName)
fprintf(fid, '%s %d ', somaChanName{j}, somaChanCond(j));
end
%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
%% Create morphology
fprintf(fid, ['\n\n*compt /library/' libName '/prim_dend\n']);
for j=1:3
fprintf(fid, ['primdend' num2str(j) ' soma ' num2str(pLen) ' 0 0 1\n']);
end
fprintf(fid, ['\n*compt /library/' libName '/sec_dend\n']);
for j=1:6
fprintf(fid, ['secdend' num2str(j) ...
' primdend' num2str(floor((j+1)/2)) '/prim_dend2' ...
' ' num2str(sLen) ' 0 0 0.75\n']);
end
fprintf(fid, ['\n*compt /library/' libName '/tert_dend\n']);
for j=1:12
fprintf(fid, ['tertdend' num2str(j) ...
' secdend' num2str(floor((j+1)/2)) '/sec_dend4' ...
' ' num2str(tLen) ' 0 0 0.5\n']);
end
fclose(fid);
end