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limo_mglm.m
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limo_mglm.m
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function model = limo_mglm(varargin)
% Multivariate General Linear Model for EEG data
% The model consider subjects / trials as independent observations
% i.e. this is similar as running a N-way MANOVA or MANCOVA
% Analyses are performed at one time frame only, but for all
% subjects/ trials and considering the pattern of effect across all electrodes.
% In addition, we compute the multivariate Discriminable value D which allows
% finding if conditions/regressors (classes) are different. This is similar
% as a pattern classification (LDA, SVM etc) without to have to reply on
% particular classifier algorithm.
%
% FORMAT:
% model = limo_mglm(Y,LIMO)
% model = limo_mglm(Y,X,nb_conditions,nb_interactions,nb_continuous,method,W)
%
% INPUTS:
% Y = 2D matrix of EEG data with format trials/subjects x electrodes
% LIMO = structure that contains the information below (except Y)
% or input info that are in LIMO.mat
% X = 2 dimensional design matrix
% nb_conditions = a vector indicating the number of conditions per factor
% nb_interactions = a vector indicating number of columns per interactions
% nb_continuous = number of covariates
% method = 'OLS', 'WLS', 'IRLS' (bisquare)
% W = optional - a matrix a trial weights ; ie method 'WLS'
% using these weights rather than something else
%
% OUTPUTS:
% model.MANOVA.R2.V
% model.MANOVA.R2.EV
% model.MANOVA.R2.Roy.F
% model.MANOVA.R2.Roy.p
% model.MANOVA.R2.Pillai.F
% model.MANOVA.R2.Pillai.p
% model.MANOVA.betas = the beta parameters (dimensions nb of paramters x electrodes)
% model.MANOVA.conditions = categorical effects
% --> F/p in rows are the factors, in columns time frames
% --> df row 1 = df, row 2 = dfe, columns are factors
% model.MANOVA.continuous = continuous effects
% --> F/p in rows are the variables, in columns time frames
% --> df column 1 = df, column2 2 = dfe (same for all covariates)
%
% model.Classification.D
% model.Classification.cvD
% model.Classification.D
%
% NOTES:
%
% The parameters can be computed using 3 methods: ordinary least squares,
% weighted least squares and iterative reweighted least squares.
% For OLS, W=ones(size(Y)), for IRLS and WLS the weights can be provided.
% For IRLS, each cell (time and space) is weighted so it doesn't matter if
% precomputed by limo_eeg.m *unless you want to pass some special weights)
% For WLS, the default from limo_eeg.m is that weights are computed
% trial-wise, seeing a trial as multivariate in time, but then the MANOVA is computed
% across electrodes (ie all electrode have the same weights). If W is not provided,
% the weights will be computed across electrodes, seeing a trial as a multivariate
% measures in space.
%
% Within the MGLM, each effect is accounted for given the other effects; this means
% that one can have a different number of trials/subjects per conditions/factors
% provided there is no interactions - for interactions this is not possible
% and no correction is provided - a design created by limo_design_matrix
% would have sampled trials to make sure the number of trials is identical
% across interaction terms.
%
% The multivariate statistic uses Pillais' V and Roy's
% test. In Roy's test one maximizes the spread of the transformed data using the
% 1st eigen value of inv(E)*H. The F approximation is an upper bound, i.e.
% results are safe if H0 is accepted (no effect) but not rejected. If data
% are highly correlated, there is only one high eigen value and Roy test is
% appropriate otherwise Pillai is better.
%
% The Classification ...
%
% References
% Christensen, R. 2002. Plane answers to complex questions. 3rd Ed. Springer-Verlag
% Friston et al. 2007. Statitical Parametric Mapping. Academic Press
% Rencher, A.C. 2002. Methods of Multivariate Analysis. 2nd Ed. Wiley.
% Robert and Escoufier, 1976. J.Royal Stat Soc, C
% Pernet et al. in prep. Classification of EEG data though MGLM.
%
% See also
% LIMO_DESIGN_MATRIX, LIMO_PCOUT, LIMO_IRLS, LIMO_EEG, LIMO_DECOMP
%
% Cyril Pernet v1 13-05-2013
% ----------------------------
% Copyright (C) LIMO Team 2014
%% varagin
W = [];
if nargin == 2
Y = varargin{1};
X = varargin{2}.design.X;
nb_conditions = varargin{2}.design.nb_conditions;
nb_interactions = varargin{2}.design.nb_interactions;
nb_continuous = varargin{2}.design.nb_continuous;
method = varargin{2}.design.method;
try
W = varargin{2}.design.weigths;
end
elseif nargin >= 6
Y = varargin{1};
X = varargin{2};
nb_conditions = varargin{3};
nb_interactions = varargin{4};
nb_continuous = varargin{5};
method = varargin{6};
if nargin == 7
W = varargin(7);
end
else
error('varargin error')
end
nb_factors = numel(nb_conditions);
if nb_factors == 1 && nb_conditions == 0
nb_factors = 0;
end
% -----------
%% Data check
% -----------
if size(Y,1)~=size(X,1)
error('The number of events in Y and the design matrix are different')
end
if nb_interactions == 0
nb_interactions = [];
end
% ------------------------------
%% Compute F for dummy variables
% ------------------------------
% -------------------------
if nb_factors == 1 % 1-way MANOVA
% -------------------------
% total sum of squares, projection matrix for errors, residuals and betas
% -----------------------------------------------------------------------
T = (Y-repmat(mean(Y),size(Y,1),1))'*(Y-repmat(mean(Y),size(Y,1),1)); % SS Total
R = eye(size(Y,1)) - (X*pinv(X)); % Projection on E
E = (Y'*R*Y); % SS Error
% compute Beta parameters and weights
if strcmp(method,'OLS')
W = ones(size(Y,1),1);
Betas = pinv(X)*Y;
elseif strcmp(method,'WLS')
if isempty(W)
[Betas,W] = limo_WLS(X,Y);
else
Betas = pinv(WX)*WY;
end
elseif strcmp(method,'IRLS')
[Betas,W] = limo_IRLS(X,Y);
end
% compute model R^2
% -----------------
C = eye(size(X,2));
C(:,size(X,2)) = 0;
C0 = eye(size(X,2)) - C*pinv(C);
X0 = X*C0; % Reduced model
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R; % Projection matrix onto Xc
H = (Betas'*X'*M*X*Betas); % SS Effect
% Generalized R2
% variance covariance matrix
S = cov([Y X(:,1:size(X,2)-1)]);
Syy = S(1:size(Y,2),1:size(Y,2));
Sxy = S(size(Y,2)+1:size(S,1),1:size(Y,2));
Syx = S(1:size(Y,2),size(Y,2)+1:size(S,2));
Sxx = S(size(Y,2)+1:size(S,1),size(Y,2)+1:size(S,2));
Rsquare_multi = trace(Sxy*Syx) / sqrt(trace(Sxx.^2)*trace(Syy.^2)); % Robert and Escoufier, J.Royal Stat Soc, C - 1976
Eigen_values_R2 = limo_decomp(E,H);
p = size(Y,2); % = number of variables (dimension)
q = rank(X); % = number of regressors (df)
s = min(p,q); % df
n = size(Y,1); % nb of observations (dfe)
m = (abs(q-p)-1)/2;
N = (n-q-p-2)/2;
d = max(p,q);
theta = max(Eigen_values_R2) / (1+max(Eigen_values_R2)); % Roy
R2_Roy_value = theta; % = 1st canonical correlation
R2_Roy_F = ((n-d-1)*max(Eigen_values_R2))/d;
R2_Roy_p = 1-fcdf(R2_Roy_F, d, (n-d-1));
V = sum(Eigen_values_R2 ./ (1+Eigen_values_R2)); % Pillai
R2_Pillai_value = V / s; % average of canonical correlations
R2_Pillai_F = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
R2_Pillai_p = 1-fcdf(R2_Pillai_F,(s*(2*m+s+1)),(s*(2*N+s+1)));
% compute F for categorical variables
% -----------------------------------
if nb_conditions ~= 0 && nb_continuous == 0
Eigen_values_cond = Eigen_values_R2;
elseif nb_conditions ~= 0 && nb_continuous ~= 0
C = eye(size(X,2));
C(:,(nb_conditions+1):size(X,2)) = 0;
C0 = eye(size(X,2)) - C*pinv(C);
X0 = X*C0; % Here the reduced model includes the covariates
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R;
H = (Betas'*X'*M*X*Betas);
[Eigen_vectors_cond,Eigen_values_cond] = limo_decomp(E,H);
end
model.conditions.EV = [Eigen_values_cond'];
vh = nb_conditions - 1; % df = q above
s = min(vh,p); % subspace in which mean Ys are located
for c=1:nb_conditions
nb_items(c) = numel(find(X(:,c)));
end
if sum(nb_items == nb_items(1)) == length(nb_items)
ve = nb_conditions*(nb_items(1)-1); % dfe equal sample sizes
else
ve = sum(nb_items) - nb_conditions; % dfe different sample sizes
end
if s > 1
m = (abs(vh-p)-1)/2;
N = (ve-p-1) / 2;
% Pillai
V = sum(Eigen_values_cond ./ (1+Eigen_values_cond));
df_conditions_Pillai = s*(2*m+s+1);
dfe_conditions_Pillai = s*(2*N+s+1);
F_conditions_Pillai = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
pval_conditions_Pillai = 1-fcdf(F_conditions_Pillai,df_conditions_Pillai,dfe_conditions_Pillai);
% Roy's test
theta = max(Eigen_values_cond) / (1+max(Eigen_values_cond));
df_conditions_Roy = max(p,vh);
dfe_conditions_Roy = ve - 1; % in Renchner it is proposed to use ve - max(p,vh) -1 while in Statistica it is ve -1
F_conditions_Roy = (dfe_conditions_Roy*max(Eigen_values_cond))/df_conditions_Roy;
pval_conditions_Roy = 1-fcdf(F_conditions_Roy, df_conditions_Roy, dfe_conditions_Roy);
else % = only one non zeros Eigen value s = 1 and/or vh = 1
V = sum(Eigen_values_cond ./ (1+Eigen_values_cond));
U = max(Eigen_values_cond);
theta = U;
df_conditions_Pillai = p; % number of frames
dfe_conditions_Pillai = ve-p+1;
df_conditions_Roy = df_conditions_Pillai;
dfe_conditions_Roy = dfe_conditions_Pillai;
F_conditions_Pillai = (dfe_conditions_Pillai/df_conditions_Pillai) * max(Eigen_values_cond);
pval_conditions_Pillai = 1-fcdf(F_conditions_Pillai,df_conditions_Pillai,dfe_conditions_Pillai);
F_conditions_Roy = F_conditions_Pillai;
pval_conditions_Roy = pval_conditions_Pillai;
end
% compute the discriminant function
% ---------------------------------
if length(Y)-nb_conditions <= nb_conditions
errordlg('there is not enough data point to run a discriminant analysis')
else
a = inv(chol(E))*Eigen_vectors_cond; % need to adjust eigen vectors
weights = Eigen_values_cond ./ sum(Eigen_values_cond);
% get the function(s)
for d=1:size(a,2)
z(:,d) = a(:,d)'*Y;
end
% do the classification
end
% ------------------------------------------------
elseif nb_factors > 1 && isempty(nb_interactions) % N-ways MANOVA without interactions
% ------------------------------------------------
% compute basic SS total, projection matrices and parameters
T = (Y-repmat(mean(Y),size(Y,1),1))'*(Y-repmat(mean(Y),size(Y,1),1));
R = eye(size(Y,1)) - (X*pinv(X));
E = (Y'*R*Y);
% compute Beta parameters and weights
if strcmp(method,'OLS')
W = ones(size(Y,1),1);
Betas = pinv(X)*Y;
elseif strcmp(method,'WLS')
if isempty(W)
[Betas,W] = limo_WLS(X,Y);
else
Betas = pinv(WX)*WY;
end
elseif strcmp(method,'IRLS')
[Betas,W] = limo_IRLS(X,Y);
end
% --------------------
% compute model R^2
% --------------------
C = eye(size(X,2));
C(:,size(X,2)) = 0;
C0 = eye(size(X,2)) - C*pinv(C);
X0 = X*C0; % Reduced model (i.e. only intercept)
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R; % M is the projection matrix onto Xc
H = (Betas'*X'*M*X*Betas); % SSCP Hypothesis (Effect)
Eigen_values_R2 = limo_decomp(E,H);
% Generalized R2
% variance covariance matrix
S = cov([Y X(:,1:size(X,2)-1)]);
Syy = S(1:size(Y,2),1:size(Y,2));
Sxy = S(size(Y,2)+1:size(S,1),1:size(Y,2));
Syx = S(1:size(Y,2),size(Y,2)+1:size(S,2));
Sxx = S(size(Y,2)+1:size(S,1),size(Y,2)+1:size(S,2));
Rsquare_multi = trace(Sxy*Syx) / sqrt(trace(Sxx.^2)*trace(Syy.^2)); % Robert and Escoufier, J.Royal Stat Soc, C - 1976
p = size(Y,2); % = number of variables (dimension)
q = rank(X); % = number of regressors (df)
s = min(p,q); % df
n = size(Y,1); % nb of observations (dfe)
m = (abs(q-p)-1)/2;
N = (n-q-p-2)/2;
d = max(p,q);
theta = max(Eigen_values_R2) / (1+max(Eigen_values_R2)); % Roy
R2_Roy_value = theta; % = 1st canonical correlation
R2_Roy_F = ((n-d-1)*max(Eigen_values_R2))/d;
R2_Roy_p = 1-fcdf(R2_Roy_F, d, (n-d-1));
V = sum(Eigen_values_R2 ./ (1+Eigen_values_R2)); % Pillai
R2_Pillai_value = V / s; % average of canonical correlations
R2_Pillai_F = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
R2_Pillai_p = 1-fcdf(R2_Pillai_F,(s*(2*m+s+1)),(s*(2*N+s+1)));
% --------------------------------------
% compute F and p values of each factor
% --------------------------------------
eoi = zeros(1,size(X,2));
eoi(1:nb_conditions(1)) = 1:nb_conditions(1);
eoni = [1:size(X,2)];
eoni = find(eoni - eoi);
model.conditions.EV = [];
for f = 1:length(nb_conditions)
C = eye(size(X,2));
C(:,eoni) = 0;
C0 = eye(size(X,2)) - C*pinv(C);
X0 = X*C0;
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R;
H = (Betas'*X'*M*X*Betas);
Eigen_values_cond = limo_decomp(E,H);
model.conditions.EV(f,:) = Eigen_values_cond';
vh = nb_conditions(f) - 1; % df = q above
s = min(vh,p); % subspace in which mean Ys are located
clear nb_items; x = X(:,find(eoi));
for c=1:nb_conditions(f)
nb_items(c) = numel(find(x(:,c)));
end
if sum(nb_items == nb_items(1)) == length(nb_items)
ve = nb_conditions(f)*(nb_items(1)-1); % dfe equal sample sizes
else
ve = sum(nb_items) - nb_conditions(f); % dfe different sample sizes
end
if s > 1
m = (abs(vh-p)-1)/2;
N = (ve-p-1) / 2;
% Pillai
V = sum(Eigen_values_cond ./ (1+Eigen_values_cond));
df_conditions_Pillai(f) = s*(2*m+s+1);
dfe_conditions_Pillai(f) = s*(2*N+s+1);
F_conditions_Pillai(f) = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
pval_conditions_Pillai(f) = 1-fcdf(F_conditions_Pillai(f),df_conditions_Pillai(f),dfe_conditions_Pillai(f));
% Roy's test
theta = max(Eigen_values_cond) / (1+max(Eigen_values_cond));
df_conditions_Roy(f) = max(p,vh);
dfe_conditions_Roy(f) = ve - 1; % in Renchner it is proposed to use ve - max(p,vh) -1 while in Statistica it is ve -1
F_conditions_Roy(f) = (dfe_conditions_Roy(f)*max(Eigen_values_cond))/df_conditions_Roy(f);
pval_conditions_Roy(f) = 1-fcdf(F_conditions_Roy(f), df_conditions_Roy(f), dfe_conditions_Roy(f));
else % = only one non zeros Eigen value s = 1 and/or vh = 1
V = sum(Eigen_values_cond ./ (1+Eigen_values_cond));
U = max(Eigen_values_cond);
theta = U;
df_conditions_Pillai(f) = p; % number of electrodes
dfe_conditions_Pillai(f) = ve-p+1;
df_conditions_Roy(f) = df_conditions_Pillai(f);
F_conditions_Pillai(f) = (dfe_conditions_Pillai(f)/df_conditions_Pillai(f)) * max(Eigen_values_cond);
pval_conditions_Pillai(f) = 1-fcdf(F_conditions_Pillai(f),df_conditions_Pillai(f),dfe_conditions_Pillai(f));
F_conditions_Roy(f) = F_conditions_Pillai(f);
pval_conditions_Roy(f) = pval_conditions_Pillai(f);
end
% update factors
if f<length(nb_conditions)
update = max(find(eoi));
eoi = zeros(1,size(X,2));
eoi((update+1):(update+nb_conditions(f+1))) = update + (1:nb_conditions(f+1));
eoni = [1:size(X,2)];
eoni = find(eoni - eoi);
end
end
% ------------------------------------------------
elseif nb_factors > 1 && ~isempty(nb_interactions) % N-ways MANOVA with interactions
% ------------------------------------------------
% compute basic SS total, projection matrices and parameters
T = (Y-repmat(mean(Y),size(Y,1),1))'*(Y-repmat(mean(Y),size(Y,1),1));
R = eye(size(Y,1)) - (X*pinv(X));
E = (Y'*R*Y);
if strcmp(method,'OLS')
W = ones(size(Y,1),1);
Betas = pinv(X)*Y;
elseif strcmp(method,'WLS')
if isempty(W)
[Betas,W] = limo_WLS(X,Y);
else
Betas = pinv(WX)*WY;
end
elseif strcmp(method,'IRLS')
[Betas,W] = limo_IRLS(X,Y);
end
% --------------------
% compute model R^2
% --------------------
C = eye(size(X,2));
C(:,size(X,2)) = 0;
C0 = eye(size(X,2)) - C*pinv(C);
X0 = X*C0; % Reduced model (i.e. only intercept)
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R; % M is the projection matrix onto Xc
H = (Betas'*X'*M*X*Betas); % SSCP Hypothesis (Effect)
Eigen_values_cond = limo_decomp(E,H);
% Generalized R2
% variance covariance matrix
S = cov([Y X(:,1:size(X,2)-1)]);
Syy = S(1:size(Y,2),1:size(Y,2));
Sxy = S(size(Y,2)+1:size(S,1),1:size(Y,2));
Syx = S(1:size(Y,2),size(Y,2)+1:size(S,2));
Sxx = S(size(Y,2)+1:size(S,1),size(Y,2)+1:size(S,2));
Rsquare_multi = trace(Sxy*Syx) / sqrt(trace(Sxx.^2)*trace(Syy.^2)); % Robert and Escoufier, J.Royal Stat Soc, C - 1976
Eigen_values_R2 = limo_decomp(E,H);
p = size(Y,2); % = number of variables (dimension)
q = rank(X); % = number of regressors (df)
s = min(p,q); % df
n = size(Y,1); % nb of observations (dfe)
m = (abs(q-p)-1)/2;
N = (n-q-p-2)/2;
d = max(p,q);
theta = max(Eigen_values_R2) / (1+max(Eigen_values_R2)); % Roy
R2_Roy_value = theta; % = 1st canonical correlation
R2_Roy_F = ((n-d-1)*max(Eigen_values_R2))/d;
R2_Roy_p = 1-fcdf(R2_Roy_F, d, (n-d-1));
V = sum(Eigen_values_R2 ./ (1+Eigen_values_R2)); % Pillai
R2_Pillai_value = V / s; % average of canonical correlations
R2_Pillai_F = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
R2_Pillai_p = 1-fcdf(R2_Pillai_F,(s*(2*m+s+1)),(s*(2*N+s+1)));
% ---------------------------------------------------
% start by ANOVA without interaction for main effects
% ---------------------------------------------------
% covariates
covariate_columns = [(sum(nb_conditions)+sum(nb_interactions)+1):(size(X,2)-1)];
% main effects
dummy_columns = 1:sum(nb_conditions);
% re-define X
x = [X(:,dummy_columns) X(:,covariate_columns) ones(size(X,1),1)];
% run same model as above
R = eye(size(Y,1)) - (x*pinv(x));
if strcmp(method,'IRLS')
betas = pinv(Wx)*WY;
else
w = repamt(W,1,size(Y,2));
betas = pinv(wx)*wY;
end
eoi = zeros(1,size(x,2));
eoi(1:nb_conditions(1)) = 1:nb_conditions(1);
eoni = [1:size(x,2)];
eoni = find(eoni - eoi);
model.conditions.EV = [];
for f = 1:length(nb_conditions)
C = eye(size(x,2));
C(:,eoni) = 0;
C0 = eye(size(x,2)) - C*pinv(C);
X0 = x*C0;
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R;
H(f,:) = diag((betas'*x'*M*x*betas));
Eigen_values_cond = limo_decomp(E,H);
model.conditions.EV(f,:) = Eigen_values_cond';
vh = nb_conditions(f) - 1; % df = q above
s = min(vh,p); % subspace in which mean Ys are located
clear nb_items; x = X(:,find(eoi));
for c=1:nb_conditions(f)
nb_items(c) = numel(find(x(:,c)));
end
if sum(nb_items == nb_items(1)) == length(nb_items)
ve = nb_conditions(f)*(nb_items(1)-1); % dfe equal sample sizes
else
ve = sum(nb_items) - nb_conditions(f); % dfe different sample sizes
end
if s > 1
m = (abs(vh-p)-1)/2;
N = (ve-p-1) / 2;
% Pillai
V = sum(Eigen_values_cond ./ (1+Eigen_values_cond));
df_conditions_Pillai(f) = s*(2*m+s+1);
dfe_conditions_Pillai(f) = s*(2*N+s+1);
F_conditions_Pillai(f) = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
pval_conditions_Pillai(f) = 1-fcdf(F_conditions_Pillai(f),df_conditions_Pillai(f),dfe_conditions_Pillai(f));
% Roy's test
theta = max(Eigen_values_cond) / (1+max(Eigen_values_cond));
df_conditions_Roy(f) = max(p,vh);
dfe_conditions_Roy(f) = ve - 1; % in Renchner it is proposed to use ve - max(p,vh) -1 while in Statistica it is ve -1
F_conditions_Roy(f) = (dfe_conditions_Roy(f)*max(Eigen_values_cond))/df_conditions_Roy(f);
pval_conditions_Roy(f) = 1-fcdf(F_conditions_Roy(f), df_conditions_Roy(f), dfe_conditions_Roy(f));
else % = only one non zeros Eigen value s = 1 and/or vh = 1
V = sum(Eigen_values_cond ./ (1+Eigen_values_cond));
U = max(Eigen_values_cond);
theta = U;
df_conditions_Pillai(f) = p; % number of electrodes
dfe_conditions_Pillai(f) = ve-p+1;
df_conditions_Roy(f) = df_conditions_Pillai;
dfe_conditions_Roy(f) = dfe_conditions_Pillai;
F_conditions_Pillai(f) = (dfe_conditions_Pillai/df_conditions_Pillai) * max(Eigen_values_cond);
pval_conditions_Pillai(f) = 1-fcdf(F_conditions_Pillai(f),df_conditions_Pillai(f),dfe_conditions_Pillai(f));
F_conditions_Roy(f) = F_conditions_Pillai(f);
pval_conditions_Roy(f) = pval_conditions_Pillai(f);
end
% update factors
if f<length(nb_conditions)
update = max(find(eoi));
eoi = zeros(1,size(x,2));
eoi((update+1):(update+nb_conditions(f+1))) = update + (1:nb_conditions(f+1));
eoni = [1:size(x,2)];
eoni = find(eoni - eoi);
end
end
% ---------------------------
% now deal with interactions
% ---------------------------
if nb_factors == 2 && nb_continuous == 0 % the quick way with only one interaction
HI = diag(T)' - H(1,:) - H(2,:) - diag(E)';
Eigen_values_inter = limo_decomp(E,HI);
model.interactions.EV = [Eigen_values_inter'];
vh = nb_interactions - 1; % df = q above
s = min(vh,p); % subspace in which mean Ys are located
clear nb_items; x = X(:,sum(nb_conditions)+1:end-1);
for c=1:nb_interactions
nb_items(c) = numel(find(x(:,c)));
end
if sum(nb_items == nb_items(1)) == length(nb_items)
ve = nb_interactions*(nb_items(1)-1); % dfe equal sample sizes
else
ve = sum(nb_items) - nb_interactions; % dfe different sample sizes
end
if s > 1
m = (abs(vh-p)-1)/2;
N = (ve-p-1) / 2;
% Pillai
V = sum(Eigen_values_inter ./ (1+Eigen_values_inter));
df_interaction_Pillai = s*(2*m+s+1);
dfe_interaction_Pillai = s*(2*N+s+1);
F_interaction_Pillai = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
pval_interaction_Pillai = 1-fcdf(F_interaction_Pillai,df_interaction_Pillai,dfe_interaction_Pillai);
% Roy's test
theta = max(Eigen_values_inter) / (1+max(Eigen_values_inter));
df_interaction_Roy = max(p,vh);
dfe_interaction_Roy = ve - 1; % in Renchner it is proposed to use ve - max(p,vh) -1 while in Statistica it is ve -1
F_interaction_Roy = (dfe_interaction_Roy*max(Eigen_values_cond))/df_interaction_Roy;
pval_interaction_Roy = 1-fcdf(F_interaction_Roy, df_interaction_Roy, dfe_interaction_Roy);
else % = only one non zeros Eigen value s = 1 and/or vh = 1
V = sum(Eigen_values_inter ./ (1+Eigen_values_inter));
U = max(Eigen_values_inter);
theta = U;
df_interaction_Pillai = p; % number of electrodes
dfe_interaction_Pillai = ve-p+1;
df_interaction_Roy = df_interaction_Pillai;
dfe_interaction_Roy = dfe_interaction_Pillai;
F_interaction_Pillai = (dfe_interaction_Pillai/df_interaction_Pillai) * max(Eigen_values_cond);
pval_interaction_Pillai = 1-fcdf(F_interaction_Pillai,df_interaction_Pillai,dfe_interaction_Pillai);
F_interaction_Roy = F_interaction_Pillai;
pval_interaction_Roy = pval_interaction_Pillai;
end
else % run through each interaction
% part of X unchanged
Main_effects = [X(:,dummy_columns)];
Cov_and_Mean = [X(:,covariate_columns) ones(size(Y,1),1)];
% get interactions
start = size(Main_effects,2)+1;
for i=1:length(nb_interactions)
I{i} = X(:,start:(start+nb_interactions(i)-1));
start = start+nb_interactions(i);
end
start = size(Main_effects,2)+1;
% check interaction levels
index = 1;
for n=2:nb_factors
combinations = nchoosek([1:nb_factors],n); % note it matches I above because computed with nchoosek the same way in limo_design_matrix
for c = 1:size(combinations,1)
interaction{index} = combinations(c,:);
index = index + 1;
end
end
add = 0; start_at_I = 1;
model.interactions.EV = [];
% run substituting and/or incrementing parts of X
for f = 1:length(nb_interactions)
% re-define X with interactions
test = size(interaction{f},2);
if test == 2
x = [Main_effects I{f} Cov_and_Mean]; % havbing the same nb of trials simply additive model
add = add+1;
else
if add == test
for a = start_at_I:add
Main_effects = [Main_effects I{a}];
end
start = size(Main_effects,2)+1;
start_at_I = add+1;
end
x = [Main_effects I{f} Cov_and_Mean];
end
% run same model as above
R = eye(size(Y,1)) - (x*pinv(x));
if strcmp(method,'IRLS')
betas = pinv(Wx)*WY;
else
w = repamt(W,1,size(Y,2));
betas = pinv(wx)*wY;
end
eoi = zeros(1,size(x,2));
eoi(start:(start-1+nb_interactions(f))) = start:(start-1+nb_interactions(f));
eoni = [1:size(x,2)];
eoni = find(eoni - eoi);
C = eye(size(x,2));
C(:,eoni) = 0;
C0 = eye(size(x,2)) - C*pinv(C);
X0 = x*C0;
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R;
HI(f,:) = diag((betas'*x'*M*x*betas))';
Eigen_values_inter = limo_decomp(E,HI(f,:));
model.interactions.EV(f,:) = Eigen_values_inter';
vh = nb_interactions(f) - 1; % df = q above
s = min(vh,p); % subspace in which mean Ys are located
clear nb_items; x = I{f};
for c=1:nb_interactions(f)
nb_items(c) = numel(find(x(:,c)));
end
if sum(nb_items == nb_items(1)) == length(nb_items)
ve = nb_interactions(f)*(nb_items(1)-1); % dfe equal sample sizes
else
ve = sum(nb_items) - nb_interactions(f); % dfe different sample sizes
end
if s > 1
m = (abs(vh-p)-1)/2;
N = (ve-p-1) / 2;
% Pillai
V = sum(Eigen_values_inter ./ (1+Eigen_values_inter));
df_interaction_Pillai(f) = s*(2*m+s+1);
dfe_interaction_Pillai(f) = s*(2*N+s+1);
F_interaction_Pillai(f) = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
pval_interaction_Pillai(f) = 1-fcdf(F_interaction_Pillai(f),df_interaction_Pillai(f),dfe_interaction_Pillai(f));
% Roy's test
theta = max(Eigen_values_inter) / (1+max(Eigen_values_inter));
df_interaction_Roy(f) = max(p,vh);
dfe_interaction_Roy(f) = ve - 1; % in Renchner it is proposed to use ve - max(p,vh) -1 while in Statistica it is ve -1
F_interaction_Roy(f) = (dfe_interaction_Roy(f)*max(Eigen_values_cond))/df_interaction_Roy(f);
pval_interaction_Roy(f) = 1-fcdf(F_interaction_Roy(f), df_interaction_Roy(f), dfe_interaction_Roy(f));
else % = only one non zeros Eigen value s = 1 and/or vh = 1
V = sum(Eigen_values_inter ./ (1+Eigen_values_inter));
U = max(Eigen_values_inter);
theta = U;
df_interaction_Pillai(f) = p; % number of electrodes
dfe_interaction_Pillai(f) = ve-p+1;
df_interaction_Roy(f) = df_interaction_Pillai(f);
dfe_interaction_Roy(f) = dfe_interaction_Pillai(f);
F_interaction_Pillai(f) = (dfe_interaction_Pillai(f)/df_interaction_Pillai(f)) * max(Eigen_values_cond);
pval_interaction_Pillai(f) = 1-fcdf(F_interaction_Pillai(f),df_interaction_Pillai(f),dfe_interaction_Pillai(f));
F_interaction_Roy(f) = F_interaction_Pillai(f);
pval_interaction_Roy(f) = pval_interaction_Pillai(f);
end
end
end
end
% -----------------------------------
%% compute F for continuous variables
% -----------------------------------
if nb_continuous ~=0
if nb_factors == 0
T = (Y-repmat(mean(Y),size(Y,1),1))'*(Y-repmat(mean(Y),size(Y,1),1));
R = eye(size(Y,1)) - (X*pinv(X));
E = (Y'*R*Y);
if strcmp(method,'OLS')
W = ones(size(Y,1),1);
Betas = X\Y; % numerically more stable than pinv
elseif strcmp(method,'WLS')
if isempty(W)
[Betas,W] = limo_WLS(X,Y);
else
Betas = pinv(WX)*WY;
end
elseif strcmp(method,'IRLS')
[Betas,W] = limo_IRLS(X,Y);
end
% compute model R^2
% -----------------
C = eye(size(X,2));
C(:,size(X,2)) = 0;
C0 = eye(size(X,2)) - C*pinv(C);
X0 = X*C0;
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R;
H = (Betas'*X'*M*X*Betas);
Eigen_values_R2 = limo_decomp(E,H);
% Generalized R2
% variance covariance matrix
S = cov([Y X(:,1:size(X,2)-1)]);
Syy = S(1:size(Y,2),1:size(Y,2));
Sxy = S(size(Y,2)+1:size(S,1),1:size(Y,2));
Syx = S(1:size(Y,2),size(Y,2)+1:size(S,2));
Sxx = S(size(Y,2)+1:size(S,1),size(Y,2)+1:size(S,2));
Rsquare_multi = trace(Sxy*Syx) / sqrt(trace(Sxx.^2)*trace(Syy.^2)); % Robert and Escoufier, J.Royal Stat Soc, C - 1976
Eigen_values_R2 = limo_decomp(E,H);
p = size(Y,2); % = number of variables (dimension)
q = rank(X); % = number of regressors (df)
s = min(p,q); % df
n = size(Y,1); % nb of observations (dfe)
m = (abs(q-p)-1)/2;
N = (n-q-p-2)/2;
d = max(p,q);
theta = max(Eigen_values_R2) / (1+max(Eigen_values_R2)); % Roy
R2_Roy_value = theta; % = 1st canonical correlation
R2_Roy_F = ((n-d-1)*max(Eigen_values_R2))/d;
R2_Roy_p = 1-fcdf(R2_Roy_F, d, (n-d-1));
V = sum(Eigen_values_R2 ./ (1+Eigen_values_R2)); % Pillai
R2_Pillai_value = V / s; % average of canonical correlations
R2_Pillai_F = ((2*N+s+1)*V) / ((2*m+s+1)*(s-V)');
R2_Pillai_p = 1-fcdf(R2_Pillai_F,(s*(2*m+s+1)),(s*(2*N+s+1)));
else
% compute
nb_conditions = sum(nb_conditions) + sum(nb_interactions);
model.continuous.EV = [];
for n = 1:nb_continuous
C = zeros(size(X,2));
C(nb_conditions+n,nb_conditions+n) = 1;
C0 = eye(size(X,2)) - C*pinv(C);
X0 = X*C0;
R0 = eye(size(Y,1)) - (X0*pinv(X0));
M = R0 - R;
H = Betas'*X'*M*X*Betas;
Eigen_values_continuous = limo_decomp(E,H);
model.continuous.EV = [model.continuous.EV Eigen_values_continuous'];
df_continuous = size(Y,2);
dfe_continuous = size(Y,1)-nb_continuous-size(Y,2);
if nb_conditions ~= 0
dfe_continuous = dfe_continuous - length(nb_conditions);
end
s = min(size(Y,2),size(X,2));
m = (abs(size(X,2)-size(Y,2))-1) / 2;
% Roy's test
theta_continuous(n) = max(Eigen_values_continuous(:,n)) / (1+max(Eigen_values_continuous(:,n)));
F_continuous_Roy(n) = (dfe_continuous*max(Eigen_values_continuous(:,n)))/df_continuous;
pval_continuous_Roy(n) = 1-fcdf(F_continuous_Roy(n), df_continuous, dfe_continuous);
% Pillai
V_continuous(n) = sum(Eigen_values_continuous(:,n) ./ (1+Eigen_values_continuous(:,n)));
F_continuous_Pillai(n) = F_continuous_Roy(n);
pval_continuous_Pillai(n) = pval_continuous_Roy(n);
end
end
end
% ----------------------------
%% update the model structure
% ----------------------------
model.R2.V = Rsquare_multi;
model.R2.EV = Eigen_values_R2;
model.R2.Roy.F = R2_Roy_F;
model.R2.Roy.p = R2_Roy_p;
model.R2.Pillai.F = R2_Pillai_F;
model.R2.Pillai.p = R2_Pillai_p;
model.betas = Betas;
if nb_conditions ~= 0
model.conditions.Pillai.F = F_conditions_Pillai;
model.conditions.Pillai.p = pval_conditions_Pillai;
model.conditions.Pillai.df = df_conditions_Pillai;
model.conditions.Pillai.dfe = dfe_conditions_Pillai;
model.conditions.Roy.F = F_conditions_Roy;
model.conditions.Roy.p = pval_conditions_Roy;
model.conditions.Roy.df = df_conditions_Roy;
model.conditions.Roy.dfe = dfe_conditions_Roy;
end
if nb_interactions ~= 0
model.interactions.Pillai.F = F_interactions_Pillai;
model.interactions.Pillai.p = pval_interactions_Pillai;
model.interactions.Pillai.df = df_interactions_Pillai;
model.interactions.Pillai.dfe = dfe_interactions_Pillai;
model.interactions.Roy.F = F_interactions_Roy;
model.interactions.Roy.p = pval_interactions_Roy;
model.interactions.Roy.df = df_interactions_Roy;
model.interactions.Roy.dfe = dfe_interactions_Roy;
end
if nb_continuous > 0
model.continuous.Pillai.F = F_continuous_Pillai;
model.continuous.Pillai.p = pval_continuous_Pillai;
model.continuous.Pillai.df = df_continuous;
model.continuous.Pillai.dfe = dfe_continuous;
model.continuous.Roy.F = F_continuous_Roy;
model.continuous.Roy.p = pval_continuous_Roy;
model.continuous.Roy.df = df_continuous;
model.continuous.Roy.dfe = dfe_continuous;
end