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ft_denoise_tsr.m
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ft_denoise_tsr.m
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function dataout = ft_denoise_tsr(cfg, varargin)
% FT_DENOISE_TSR performs a regression analysis, using a (time-shifted set
% of) reference signal(s) as independent variable. It is a generic
% implementation of the method described by De Cheveigne
% (https://doi.org/10.1016/j.jneumeth.2007.06.003), or can be
% used to compute temporal-response-functions (see e.g. Crosse
% (https://doi.org/10.3389/fnhum.2016.00604)), or
% spatial filters based on canonical correlation (see Thielen
% (https://doi.org/10.1371/journal.pone.0133797))
%
% Use as
% [dataout] = ft_denoise_tsr(cfg, data)
% [dataout] = ft_denoise_tsr(cfg, data, refdata)
% where "data" is a raw data structure that was obtained with FT_PREPROCESSING. If
% you specify the additional input "refdata", the specified reference channels for
% the regression will be taken from this second data structure. This can be useful
% when reference-channel specific preprocessing needs to be done (e.g. low-pass
% filtering).
%
% The output structure dataout contains the denoised data in a format consistent
% with the output of FT_PREPROCESSING.
%
% The configuration options are:
% cfg.refchannel = the channels used as reference signal (default = 'MEGREF'), see FT_SELECTDATA
% cfg.channel = the channels to be denoised (default = 'all'), see FT_SELECTDATA
% cfg.method = string, 'mlr', 'cca', 'pls', 'svd', option specifying the criterion for the regression
% (default = 'mlr')
% cfg.reflags = integer array, specifying temporal lags (in msec) by which to shift refchannel
% with respect to data channels
% cfg.trials = integer array, trials to be used in regression, see FT_SELECTDATA
% cfg.testtrials = cell-array or string, trial indices to be used as test folds in a cross-validation scheme
% (numel(cfg.testrials == number of folds))
% cfg.nfold = scalar, indicating the number of test folds to
% use in a cross-validation scheme
% cfg.standardiserefdata = string, 'yes' or 'no', whether or not to standardise reference data
% prior to the regression (default = 'no')
% cfg.standardisedata = string, 'yes' or 'no', whether or not to standardise dependent variable
% prior to the regression (default = 'no')
% cfg.demeanrefdata = string, 'yes' or 'no', whether or not to make
% reference data zero mean prior to the regression (default = 'no')
% cfg.demeandata = string, 'yes' or 'no', whether or not to make
% dependent variable zero mean prior to the regression (default = 'no')
% cfg.threshold = integer array, ([1 by 2] or [1 by numel(cfg.channel) + numel(cfg.reflags)]),
% regularization or shrinkage ('lambda') parameter to be loaded on the diagonal of the
% penalty term (if cfg.method == 'mlrridge' or 'mlrqridge')
% cfg.updatesens = string, 'yes' or 'no' (default = 'yes')
% cfg.perchannel = string, 'yes' or 'no', or logical, whether or not to perform estimation of beta weights
% separately per channel
% cfg.output = string, 'model' or 'residual' (defaul = 'model'),
% specifies what is outputed in .trial field in <dataout>
% cfg.performance = string, 'Pearson' or 'r-squared' (default =
% 'Pearson'), indicating what performance metric is outputed in .weights(k).performance
% field of <dataout> for the k-th fold
%
% If cfg.threshold is 1 x 2 integer array, the cfg.threshold(1) parameter scales
% uniformly in the dimension of predictor variable and cfg.threshold(2) in the
% space of response variable.
%
% See also FT_PREPROCESSING, FT_DENOISE_SYNTHETIC, FT_DENOISE_PCA
% Copyright (c) 2008-2009, Jan-Mathijs Schoffelen, CCNi Glasgow
% Copyright (c) 2010-2011, Jan-Mathijs Schoffelen, DCCN Nijmegen
% Copyright (c) 2018, Jan-Mathijs Schoffelen
%
% This file is part of FieldTrip, see http://www.fieldtriptoolbox.org
% for the documentation and details.
%
% FieldTrip is free software: you can redistribute it and/or modify
% it under the terms of the GNU General Public License as published by
% the Free Software Foundation, either version 3 of the License, or
% (at your option) any later version.
%
% FieldTrip is distributed in the hope that it will be useful,
% but WITHOUT ANY WARRANTY; without even the implied warranty of
% MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
% GNU General Public License for more details.
%
% You should have received a copy of the GNU General Public License
% along with FieldTrip. If not, see <http://www.gnu.org/licenses/>.
%
% $Id$
% UNDOCUMENTED OPTIONS (or possibly unused)
% cfg.testsamples
% cfg.truncate
% cfg.trials
%
% === cfg.truncate
% if cfg.truncate is integer n > 1, n will be the number of singular values kept.
% if 0 < cfg.truncate < 1, the singular value spectrum will be thresholded at the
% fraction cfg.truncate of the explained variance.
% these are used by the ft_preamble/ft_postamble function and scripts
ft_revision = '$Id$';
ft_nargin = nargin;
ft_nargout = nargout;
% do the general setup of the function
ft_defaults
ft_preamble init
ft_preamble debug
ft_preamble provenance varargin
ft_preamble trackconfig
% the ft_abort variable is set to true or false in ft_preamble_init
if ft_abort
return
end
% check if the input data is valid for this function
for i=1:length(varargin)
varargin{i} = ft_checkdata(varargin{i}, 'datatype', 'raw');
end
% check if the input cfg is valid for this function
cfg = ft_checkconfig(cfg, 'forbidden', {'channels', 'trial'}); % prevent accidental typos, see issue 1729
% set the defaults
cfg.nfold = ft_getopt(cfg, 'nfold', 1);
cfg.blocklength = ft_getopt(cfg, 'blocklength', 'trial');
cfg.testtrials = ft_getopt(cfg, 'testtrials', 'all');
cfg.testsamples = ft_getopt(cfg, 'testsamples', 'all');
cfg.refchannel = ft_getopt(cfg, 'refchannel', '');
cfg.reflags = ft_getopt(cfg, 'reflags', 0); %this needs to be known for the folding
% set the rest of the defaults
cfg.channel = ft_getopt(cfg, 'channel', 'all');
cfg.truncate = ft_getopt(cfg, 'truncate', 'no');
cfg.standardiserefdata = ft_getopt(cfg, 'standardiserefdata', 'no');
cfg.standardisedata = ft_getopt(cfg, 'standardisedata', 'no');
cfg.demeanrefdata = ft_getopt(cfg, 'demeanrefdata', 'no');
cfg.demeandata = ft_getopt(cfg, 'demeandata', 'no');
cfg.trials = ft_getopt(cfg, 'trials', 'all', 1);
cfg.feedback = ft_getopt(cfg, 'feedback', 'none');
cfg.updatesens = ft_getopt(cfg, 'updatesens', 'yes');
cfg.perchannel = ft_getopt(cfg, 'perchannel', 'yes');
cfg.method = ft_getopt(cfg, 'method', 'mlr');
cfg.threshold = ft_getopt(cfg, 'threshold', 0);
cfg.output = ft_getopt(cfg, 'output', 'model');
cfg.performance = ft_getopt(cfg, 'performance', 'Pearson');
if ~iscell(cfg.refchannel)
cfg.refchannel = {cfg.refchannel};
end
if iscell(cfg.testtrials)
% this has precedence above nfold
cfg.nfold = numel(cfg.testtrials);
end
if cfg.nfold<=1
dataout = ft_denoise_tsr_core(cfg, varargin{:});
else
% do a cross validation
if numel(varargin{1}.trial)>1 && ischar(cfg.blocklength) && isequal(cfg.blocklength, 'trial')
if ~iscell(cfg.testtrials)
% create sets of trial indices for the test data
ntrl = numel(varargin{1}.trial);
edges = round(linspace(0,ntrl,cfg.nfold+1));
indx = randperm(ntrl);
cfg.testtrials = cell(1,cfg.nfold);
for k = 1:cfg.nfold
cfg.testtrials{k} = indx((edges(k)+1):edges(k+1));
end
end
testtrials = cfg.testtrials;
tmp = cell(1,numel(testtrials));
for k = 1:numel(testtrials)
fprintf('estimating model for fold %d/%d\n', k, numel(testtrials));
cfg.testtrials = testtrials{k};
tmp{k} = ft_denoise_tsr_core(cfg, varargin{:});
end
% create output data structure
dataout = keepfields(tmp{1}, {'fsample' 'label'});
for k = 1:numel(testtrials)
tmp{k}.weights.trials = testtrials{k};
dataout.trial(testtrials{k}) = tmp{k}.trial;
dataout.time(testtrials{k}) = tmp{k}.time;
dataout.weights(k) = tmp{k}.weights;
dataout.cfg.previous{k} = tmp{k}.cfg;
if isfield(tmp{k}, 'trialinfo')
dataout.trialinfo(testtrials{k},:) = tmp{k}.trialinfo;
end
end
elseif numel(varargin{1}.trial==1) ||(numel(varargin{1}.trial)>1 && ~ischar(cfg.blocklength))
% concatenate into a single trial, with sufficient nan-spacing to
% accommodate the shifting, and do a chunk-based folding
error('not yet implemented');
else
error('incorrect specification of data and cfg.blocklength');
end
end
% do the general cleanup and bookkeeping at the end of the function
ft_postamble debug
ft_postamble trackconfig
ft_postamble previous varargin
ft_postamble provenance dataout
ft_postamble history dataout
ft_postamble savevar dataout
%-------------------------------------------------
function dataout = ft_denoise_tsr_core(cfg, varargin)
% create a separate structure for the reference data
tmpcfg = keepfields(cfg, {'trials', 'showcallinfo', 'trackcallinfo', 'trackconfig', 'trackusage', 'trackdatainfo', 'trackmeminfo', 'tracktimeinfo'});
tmpcfg.channel = cfg.refchannel;
if numel(varargin)>1
fprintf('selecting reference channel data from the second data input argument\n');
refdata = ft_selectdata(tmpcfg, varargin{2});
else
fprintf('selecting reference channel data from the first data input argument\n');
refdata = ft_selectdata(tmpcfg, varargin{1});
end
[dum, refdata] = rollback_provenance(cfg, refdata);
% keep the requested channels from the data
tmpcfg = keepfields(cfg, {'trials', 'channel', 'showcallinfo', 'trackcallinfo', 'trackconfig', 'trackusage', 'trackdatainfo', 'trackmeminfo', 'tracktimeinfo'});
data = ft_selectdata(tmpcfg, varargin{1});
[cfg, data] = rollback_provenance(cfg, data);
% deal with the specification of testtrials/testsamples, as per the
% instruction by the caller function, for cross-validation purposes
if ~ischar(cfg.testtrials) && ischar(cfg.testsamples) && isequal(cfg.testsamples, 'all')
% subselect trials for testing
usetestdata = true;
tmpcfg = [];
tmpcfg.trials = cfg.testtrials;
testdata = ft_selectdata(tmpcfg, data);
testrefdata = ft_selectdata(tmpcfg, refdata);
tmpcfg.trials = setdiff(1:numel(data.trial), cfg.testtrials);
data = ft_selectdata(tmpcfg, data);
refdata = ft_selectdata(tmpcfg, refdata);
elseif ~ischar(cfg.testsamples) && ischar(cfg.testtrials) && isequal(cfg.testtrials, 'all')
% subselect samples from a single trial for testing
usetestdata = true;
elseif ischar(cfg.testtrials) && ischar(cfg.testsamples)
% just a single fold, use all data for training and testing
usetestdata = false;
else
error('something wrong here');
end
% demean
if istrue(cfg.demeanrefdata)
fprintf('demeaning the reference channels\n');
mu_refdata = cellmean(refdata.trial, 2);
refdata.trial = cellvecadd(refdata.trial, -mu_refdata);
if usetestdata
mu_testrefdata = cellmean(testrefdata.trial, 2);
testrefdata.trial = cellvecadd(testrefdata.trial, -mu_testrefdata);
end
end
if istrue(cfg.demeandata)
fprintf('demeaning the data channels\n');
mu_data = cellmean(data.trial, 2);
data.trial = cellvecadd(data.trial, -mu_data);
if usetestdata
mu_testdata = cellmean(testdata.trial, 2);
testdata.trial = cellvecadd(testdata.trial, -mu_testdata);
end
end
% do the time shifting for the reference channel data
ft_hastoolbox('cellfunction', 1);
timestep = mean(diff(data.time{1}));
reflags = -unique(round(cfg.reflags./timestep));
reflabel = refdata.label; % to be used later
% the convention is to have a positive cfg.reflags defined as a delay of the ref w.r.t. the chan
% cellshift has an opposite convention with respect to the sign of the
% delay, hence the minus
if ~any(reflags==0)
ft_error('the time lags for the reference data should at least include the sample 0');
end
fprintf('shifting the reference data\n');
refdata.trial = cellshift(refdata.trial, reflags, 2, [], 'overlap');
refdata.time = cellshift(data.time, 0, 2, [abs(min(reflags)) abs(max(reflags))], 'overlap');
refdata.label = repmat(refdata.label,numel(reflags),1);
for k = 1:numel(refdata.label)
refdata.label{k} = sprintf('%s_shift%03d',refdata.label{k}, k);
end
% center the data on lag 0
data.trial = cellshift(data.trial, 0, 2, [abs(min(reflags)) abs(max(reflags))], 'overlap');
data.time = cellshift(data.time, 0, 2, [abs(min(reflags)) abs(max(reflags))], 'overlap');
% only keep the trials that have > 0 samples
tmpcfg = [];
tmpcfg.trials = find(cellfun('size',data.trial,2)>0);
data = ft_selectdata(tmpcfg, data);
[cfg, data] = rollback_provenance(cfg, data);
refdata = ft_selectdata(tmpcfg, refdata);
[dum,refdata] = rollback_provenance(cfg, refdata);
% standardise the data
if istrue(cfg.standardiserefdata)
fprintf('standardising the reference channels \n');
[refdata.trial, std_refdata] = cellzscore(refdata.trial, 2, 0);
else
std_refdata = ones(numel(refdata.label),1);
end
if istrue(cfg.standardisedata)
fprintf('standardising the data channels \n');
[data.trial, std_data] = cellzscore(data.trial, 2, 0);
else
std_data = ones(numel(data.label),1);
end
% demean again, just to be sure
if istrue(cfg.demeanrefdata)
fprintf('demeaning the reference channels\n');
mu_refdata = cellmean(refdata.trial, 2);
refdata.trial = cellvecadd(refdata.trial, -mu_refdata);
end
if istrue(cfg.demeandata)
fprintf('demeaning the data channels\n'); % the edges have been chopped off
mu_data = cellmean(data.trial, 2);
data.trial = cellvecadd(data.trial, -mu_data);
end
% compute the covariance
fprintf('computing the covariance\n');
nref = size(refdata.trial{1},1);
nchan = numel(data.label);
C = nan(nchan,nchan);
C(1:nchan,1:nchan) = nancov(data.trial, data.trial, 1, 2, 1);
C(1:nchan,nchan+(1:nref)) = nancov(data.trial, refdata.trial, 1, 2, 1);
C(nchan+(1:nref),1:nchan) = C(1:nchan,nchan+(1:nref)).';
C(nchan+(1:nref),nchan+(1:nref)) = nancov(refdata.trial, refdata.trial, 1, 2, 1);
% compute the regression
if istrue(cfg.perchannel)
beta_ref = zeros(nchan, nref);
rho = zeros(nchan,1);
for k = 1:nchan
indx = [k nchan+(1:nref)];
[E, rho(k)] = multivariate_decomp(C(indx,indx), 1+(1:nref), 1, cfg.method, 1, cfg.threshold);
%beta_ref(k,:) = E(2:end)./E(1);
beta_ref(k,:) = E(2:end); %./E(1);
end
%beta_ref = (diag(rho))*beta_ref; % scale with sqrt(rho), to get the proper scaling
else
[E, rho] = multivariate_decomp(C, nchan+(1:nref), 1:nchan, cfg.method, 1, cfg.threshold);
%beta_ref = normc(E(nchan+(1:nref),:))';
%beta_data = normc(E(1:nchan,:))';
beta_ref = E(nchan+(1:nref),:);
beta_data = E(1:nchan,:);
end
% Unstandardise the data/refchannels and test data/refchannels, the
% respective std_data/std_refdata are all(ones) if the flags were false.
refdata.trial = cellvecmult(refdata.trial, std_refdata);
data.trial = cellvecmult(data.trial, std_data);
if exist('beta_data', 'var')
beta_ref = beta_ref'*diag(std_refdata);
beta_data = diag(std_data)*beta_data;
else
beta_ref = diag(std_data)*beta_ref*diag(1./std_refdata);
end
if usetestdata
fprintf('shifting the reference data for the test data\n');
testrefdata.trial = cellshift(testrefdata.trial, reflags, 2, [], 'overlap');
testrefdata.time = cellshift(testdata.time, 0, 2, [abs(min(reflags)) abs(max(reflags))], 'overlap');
testrefdata.label = repmat(testrefdata.label,numel(reflags),1);
for k = 1:numel(testrefdata.label)
testrefdata.label{k} = sprintf('%s_shift%03d',testrefdata.label{k}, k);
end
% center the data on lag 0
testdata.trial = cellshift(testdata.trial, 0, 2, [abs(min(reflags)) abs(max(reflags))], 'overlap');
testdata.time = cellshift(testdata.time, 0, 2, [abs(min(reflags)) abs(max(reflags))], 'overlap');
% demean again, just to be sure
if istrue(cfg.demeanrefdata)
fprintf('demeaning the reference channels\n');
mu_testrefdata = cellmean(testrefdata.trial, 2);
testrefdata.trial = cellvecadd(testrefdata.trial, -mu_testrefdata);
end
if istrue(cfg.demeandata)
fprintf('demeaning the data channels\n'); % the edges have been chopped off
mu_testdata = cellmean(testdata.trial, 2);
testdata.trial = cellvecadd(testdata.trial, -mu_testdata);
end
% only keep the trials that have > 0 samples
tmpcfg = [];
tmpcfg.trials = find(cellfun('size',testdata.trial,2)>0);
testdata = ft_selectdata(tmpcfg, testdata);
[dum,testdata] = rollback_provenance(cfg, testdata);
testrefdata = ft_selectdata(tmpcfg, testrefdata);
[dum,testrefdata] = rollback_provenance(cfg, testrefdata);
predicted = beta_ref*testrefdata.trial;
observed = testdata.trial;
% create output data structure
dataout = keepfields(testdata, {'cfg' 'label' 'grad' 'elec' 'opto' 'fsample' 'trialinfo'});
dataout.time = testdata.time;
else
predicted = beta_ref*refdata.trial;
if exist('beta_data', 'var')
% this is when the data multivariate
observed = beta_data'*data.trial;
else
observed = data.trial;
end
% create output data structure
dataout = keepfields(data, {'cfg' 'label' 'grad' 'elec' 'opto' 'fsample' 'trialinfo'});
dataout.time = data.time;
end
% add the time series to the output
switch cfg.output
case 'model'
dataout.trial = predicted;
case 'residual'
dataout.trial = observed - predicted;
end
% update the weights-structure
weights.time = cfg.reflags;
weights.rho = rho;
weights.covariance = C;
weights.std = [std_data;std_refdata];
if exist('beta_data', 'var')
weights.mixing = beta_data;
weights.beta = beta_ref;
else
% a per channel approach has been done, the beta weights reflect
% (channelxtime-lag) -> reshape
nref = numel(cfg.refchannel);
newbeta = zeros(size(beta_ref,1),size(beta_ref,2)./nref,nref);
for k = 1:size(newbeta,3)
newbeta(:,:,k) = beta_ref(:,k:nref:end);
end
weights.beta = newbeta;
weights.reflabel = reflabel;
weights.dimord = 'chan_lag_refchan';
end
% Compute performance statistics
fprintf('Computing performance metric\n');
switch cfg.performance
case 'Pearson'
for k = 1:size(observed{1}, 1)
tmp = nancov(cellcat(1, cellrowselect(observed,k), cellrowselect(predicted,k)), 1, 2, 1);
weights.performance(k,1) = tmp(1,2)./sqrt(tmp(1,1).*tmp(2,2));
end
case 'r-squared'
tss = nansum((observed.*isfinite(predicted)).^2, 2); % total sum of squares,
% use only the samples where both predicted and observed are non-nan, testdata are already mean subtracted in l. 330
rss = nansum((observed - predicted).^2, 2); % sum of squared residual error
% R-squared
weights.performance = (tss-rss)./tss;
end
dataout.weights = weights;