Trait anxiety is associated with reduced reward-related replay at rest
The 4 matches
- [1] § Methods › EEG analysis › Representational similarity analysis (RSA) ↔ RSA_code.zip/step01_RAS_main_code.m, lines 1–76 · score 0.85 · evoked signals, pre processed, design matrix, functional localiser, RSA, FL
- [2] § Methods › EEG analysis › Neural decoding analysis ↔ RSA_code.zip/step01_RAS_main_code.m, lines 116–254 · score 0.65 · sensor patterns, spatial correlation, intercept, sensitivity, vector, onset
- [3] § Results › Neural decoding ↔ RSA_code.zip/step01_RAS_main_code.m, lines 1–76 · score 0.61 · evoked response, functional localiser, scanning, multivariate, models, predicted
- [4] § Methods › EEG data acquisition › Data acquisition and preprocessing ↔ RSA_code.zip/step01_RAS_main_code.m, lines 116–254 · score 0.55 · EEG channel, epochs, noise, weighted, MEG, onset
Paper
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The authors' code
MATLAB · 334 lines · 15 KB · CC-BY-4.0 · 4 matches
- % RSA analysis (one GLM per sensor, where numObservations = numTrials and numPredictors = numTrialTypes)
- % RSA on the evoked signal of the functional localiser
- %
- % 1.Load in the epoched MEG data for each FL trial. Pre-processes the MEG sensor data prior to GLM
- % 2.Define the condition(stimulus)-specific sensor responses (mass univariate analysis on each sensor and timeSlice independently)
- % For each subject, sensor and timeSlice
- % 1.Dependent variable = trial*1 vector of the specific sensor*timeSlice value for each trial.
- % 1.Zscore the dependent variable pre-GLM over trials for each channel and timeBin separately. (simply rescaling the values across trials,
- % allows comparable beta value magnitudes and centring acorss the differnet independent GLMs (doen seaperately for sensorys and time bins)
- % 2.Independent variables = design matrix of trial condition ID
- % 3.Optional multivariate normalisation of the condition-specific sensor responses (1st level betas)
- % (pre-whietening of the sensor*condition betas by the multivatiate variance-covariance structure of the noise present in the sensors [which requires shrinkage if using all sensors]).
- % Diedrichsen and Kriegeskorte et al 2017, Walther et al 2016
- % 4.Choose a distance metric (Euclidian/Mahalanobis, or 1-Pearson's [corr is default])
- % 1.For each subject and time-slice a neural RDM, capturing the representational distance between the evoked responses of any two conditions
- % 2.Difference neural RDM (from 1st to second FL) captures the change in geometry from start to end of scan. Can additionally smooth the neural RM over time here, before inference.
- % 3.The difference RDM can be compared to a model RDM for position and sequence code using a regression analysis
- %
- % Matthew Nour, London, Dec 2019
- clear all;
- clc;
- close all;
- %restoredefaultpath;
- [~, pInds] = uperms([1:8],1001);
- uniquePerms=pInds;
- localiser_names = {'stimFL', 'posFL'}; % change from sFL to pFL
- numLocalisers = length(localiser_names);
- numberStates = 8;
- numberTimePoints = 85;%
- %SpecifySubjects
- numberSubjects = 68;
- numEEGChan = 64;%EEG
- eeg_channels = 1:numEEGChan;
- % Some options
- baseline_correct = 0; % demean the data for each channel and trial by the pre-stimulus baseline %%done
- multivariate_normalisation = 1; % whiten the noise structre of the condition-patterns (sensor*condition betas) before calculating the distance metric
- shrink_noise = 1; % Ledoit and Wolf, shirnkage of sample covariance matrix to avoid rank deficiency
- do_zscore = 0;
- do_demean = 1;
- cons1st = 0;
- RDM = nan(numLocalisers, numberSubjects, numberStates, numberStates, numberTimePoints, size(uniquePerms,1)); %rdm store
- chIdx_num_log = cell(numLocalisers, numberSubjects);
- load('rules_stimulus_tostate_all.mat')%%use stimulus transfer states
- load reward_index.mat
- for whichLocaliser = 1:numLocalisers
- switch localiser_names{whichLocaliser}
- case 'stimFL'
- ConDir = uigetdir('./FunctionalLocalizer_Data');
- DirCon = dir(fullfile(ConDir,'FunctionalLocalizer_*.mat')); %%%% find all the set file in your folder
- FileNamesCon = {DirCon.name};
- %
- case 'posFL'
- ConDir = uigetdir('./Position_Data');
- DirCon = dir(fullfile(ConDir,'position_*.mat')); %%%% find all the set file in your folder
- FileNamesCon = {DirCon.name};
- end
- for iSj = 1:68
- tic
- disp(['whichLocaliser = ' num2str(whichLocaliser)])
- disp(['sub = ' num2str(iSj)])
- % load the preprocessed FL/position data and identify EEG channels
- load ([ConDir,'/',char(FileNamesCon{iSj})])
- %% load labels
- stimulus_type=marker_type;
- %%stimulus transfer state
- for state=1:8
- stim=state+10;
- index_1=find(stimulus_type(:,1)==stim);
- stimulus_type(index_1)=rules_stimulus_tostate_all(iSj,state);
- end
- if reward_index(iSj,1)==1
- stimulus_type=stimulus_type;
- else
- index1=find(stimulus_type==1);
- index2=find(stimulus_type==2);
- index3=find(stimulus_type==3);
- index4=find(stimulus_type==4);
- index5=find(stimulus_type==5);
- index6=find(stimulus_type==6);
- index7=find(stimulus_type==7);
- index8=find(stimulus_type==8);
- stimulus_type(index1)=5;
- stimulus_type(index2)=6;
- stimulus_type(index3)=7;
- stimulus_type(index4)=8;
- stimulus_type(index5)=1;
- stimulus_type(index6)=2;
- stimulus_type(index7)=3;
- stimulus_type(index8)=4;
- end
- %
- %% fix the mapping from state(S1:S8) to picture_stimuli
- % this is the state ID (i.e. structural position within 2 sequences). The picID is below
- labStm_pic =stimulus_type;
- % now clean by goodchanels (lcidata = [EEGchannels, timePoints, epoched trials from all runs]
- if baseline_correct
- baseline_time = 1:11;
- for k = 1:size(stim_data,3)
- tmp = mean(stim_data(:, baseline_time(1):baseline_time(end), k), 2);
- stim_data(:, :, k) = stim_data(:, :, k) - repmat(tmp, 1, size(stim_data,2));
- end
- lcidata = stim_data;
- else
- lcidata = stim_data;
- end
- % logical vector, 1 = good channel
- chIdx = ones(numEEGChan,1);
- chIdx = logical(chIdx); % don't know why
- for iT= 1:numberTimePoints%size(lcidata,2) % time post stim onset
- % 1st level GLM on MEG data to identify stimulus-sepcific sensor weights. GLM on each sensor and iT separately, collapsing over trials
- % clear these variables every time slice
- if cons1st
- reg_log = nan(length(eeg_channels), numberStates+1);
- else
- reg_log = nan(length(eeg_channels), numberStates);
- end
- % the log of regressors over all sensors (included and excluded - 272) at this timeslice ((without intercept)
- norm_reg_log = nan(length(eeg_channels), numberStates); % (used for multivariate normalisation)
- res_log = nan(length(eeg_channels), size(lcidata,3)); % [chan * trial] log of the trial-wise residuals from the 1st level GLM for each sensor (used for multivariate normalisation)
- rdm_log = nan(numberStates,numberStates);
- for iSensor = 1:size(lcidata,1) % sensor index w.,r.t. subject-specific goodSensors
- %objective_sensor_id = chIdx_number(iSensor); % to slot into a matrix of 272 channels [or all conisdered channels] (some of which are nan, if bad)
- % reset for each sensor
- X_stim = zeros(size(lcidata,3),numberStates); % [trials * stimID)
- Y = nan(size(lcidata,3),1); % [trials * 1] = the specific sensor*iT value for each trial
- % Y - identify correct iT slice for this sensor, over all trials
- Y(:,1) = squeeze(lcidata(iSensor, iT, :)); % have already cropped the lcidata, so can index from iT take into account the epoching from -700ms
- if do_zscore
- Y = zscore(Y); % [trials * 1], MEG data zscored over all trials, per time-point and sensor (Luyckz et al 2019). This scales the Y so that it is similar for all GLM's, but does not ensure that the value of each trial (Y(t)) is scaled w.r.t. that trial's overall sensor-specific timecourse (is want this then set zscore_by_iT = 1)
- end
- if do_demean
- Y = Y-nanmean(Y); % [trials * 1], MEG data zscored over all trials, per time-point and sensor (Luyckz et al 2019). This scales the Y so that it is similar for all GLM's, but does not ensure that the value of each trial (Y(t)) is scaled w.r.t. that trial's overall sensor-specific timecourse (is want this then set zscore_by_iT = 1)
- end
- % the trial-by-trial regressor values (state ID)
- for iTrial = 1:size(lcidata,3)
- X_stim(iTrial, labStm_pic(iTrial)) = 1;
- end
- if cons1st
- design_matrix = [X_stim,ones(size(X_stim,1),1)];
- else
- design_matrix = [X_stim];
- end
- this_weights = pinv(design_matrix)*Y;
- reg_log(iSensor, :) = this_weights;
- if multivariate_normalisation
- this_residuals = Y - (design_matrix * this_weights);
- res_log(iSensor, :) = this_residuals; % [chan * trial] residuals(²Ð²î) over trials
- end
- end % end sensors
- if multivariate_normalisation
- % calculate the sensor*sensor spatial correlation structure of noise (residuals)
- trialByChanResid = squeeze(res_log(chIdx, :))'; % note the transpose (columns are random variable input to covCor)
- if shrink_noise
- [noiseCorr shrink_factor(whichLocaliser, iSj)] = covCor(trialByChanResid); % the method of Ledoit and Wolf 2004, referenced in Walther et al 2016 [shrinks the sample var-cov matirx towards the diagonal covariance matrix, to avoid rank deficiency]
- else
- noiseCorr = 1/(size(trialByChanResid,1)) * trialByChanResid' * trialByChanResid; % Walther et al 2016 (chan*chan variance-covariance matrix)
- end
- if rank(noiseCorr) < size(noiseCorr,1) % shrinking avoids rank deficiency
- warning([[char(FileNamesCon{iSj})] ' ID ' num2str(iSj) ' ' localiser_names{whichLocaliser} ' noninvertable noise covariance matrix. ? numChan < numTrials '])
- end
- % normalise the regression weights of each sensor by the
- % spatial noise correlation between sensors (the
- % vaiance-covariance matrix noiseCorr). Do this for each
- % condition separately
- for k=1:numberStates
- norm_reg_log(chIdx, k) = squeeze(reg_log(chIdx,k))' * noiseCorr^(-0.5); % post-multiply activity estimates to achieve multivariate noise normalisation (pre-whitening)
- end
- end % multivariate normalisation
- norm_reg_log_untouched = norm_reg_log(:,1:numberStates);
- reg_log_untouched = reg_log(:,1:numberStates);
- for iPerm=1:length(uniquePerms)
- % can do a lop over condition label permutaitons here
- this_perm =uniquePerms(iPerm,:);
- norm_reg_log = norm_reg_log_untouched(:,this_perm);
- reg_log = reg_log_untouched(:,this_perm);
- if multivariate_normalisation
- rdm_log(:,:) = 1-corr(squeeze(norm_reg_log(chIdx, 1:numberStates)), 'Type', 'Pearson');% dissimilarity = 1-Pearson's correlation (invariant to scaling differences, but sensitive to baseline shifts)
- rsa_log(:,:)= corr(squeeze(norm_reg_log(chIdx, 1:numberStates)), 'Type', 'Pearson');
- else
- rdm_log(:,:) = 1-corr(squeeze(reg_log(chIdx, 1:numberStates)), 'Type', 'Pearson'); % dissimilarity = 1-Pearson's correlation (invariant to scaling differences, but sensitive to baseline shifts)
- rsa_log(:,:)= corr(squeeze(reg_log(chIdx, 1:numberStates)), 'Type', 'Pearson');
- end
- RSA(whichLocaliser, iSj,:,:,iT,iPerm) = rsa_log(:,:);
- RDM(whichLocaliser, iSj,:,:,iT,iPerm) = rdm_log(:,:); % [loc, sub, 8,8 it, permNum] the resulting pairwise distances between multi-sensor patterns between each pair of conditions
- end
- end % iT
- toc
- end %subject
- end %end loop on localiser
- save(['positionALL_BC', num2str(baseline_correct), '_NORM_', num2str(multivariate_normalisation), 'SN', num2str(shrink_noise), 'Zscore', num2str(do_zscore), 'demean', num2str(do_demean), 'cons1st', num2str(cons1st)] ,'RDM','-v7.3')
- save(['positionALL_RSA_BC', num2str(baseline_correct), '_NORM_', num2str(multivariate_normalisation), 'SN', num2str(shrink_noise), 'Zscore', num2str(do_zscore), 'demean', num2str(do_demean), 'cons1st', num2str(cons1st)] ,'RSA','-v7.3')
- %% change from sFL to pFL
- dRDM =squeeze(RDM(1,:,:,:,:,:))-squeeze(RDM(2,:,:,:,:,:));
- save dRDM.mat dRDM
- %%
- clear;clc;
- load dRDM.mat
- numberSubjects=68;
- %%
- smooth_k = 3.1
- if smooth_k>0
- for iSj = 1:numberSubjects
- for iPerm = 1:1001
- dRDM_2=squeeze(dRDM(iSj,:,:,:,iPerm));
- for i1 = 1:8
- for i2 = 1:8
- if isnan(dRDM_2(i1,i2,1)) || i1<i2
- continue
- else
- if smooth_k == 1.5
- dRDM_2(i1,i2,:) = imgaussfilt(squeeze(dRDM_2(i1,i2,:)),smooth_k);
- elseif smooth_k == 3.1
- dRDM_2(i1,i2,:) = imgaussfilt(squeeze(dRDM_2(i1,i2,:)),smooth_k-0.1);
- else
- dRDM_2(i1,i2,:) = smoothdata(squeeze(dRDM_2(i1,i2,:)),'gaussian',smooth_k);
- end
- dRDM_2(i2,i1,:) = dRDM_2(i1,i2,:);
- end
- end
- end
- dRDM_new(iSj,:,:,:,iPerm)=dRDM_2;
- end
- end
- end
- save dRDM_new.mat dRDM_new
- %%
- numberSubjects = 68;
- postion_matrix=[0,0,0,0,1,0,0,0;0,0,0,0,0,1,0,0;0,0,0,0,0,0,1,0;0,0,0,0,0,0,0,1;1,0,0,0,0,0,0,0;0,1,0,0,0,0,0,0;0,0,1,0,0,0,0,0;0,0,0,1,0,0,0,0]
- postion_matrix=squareform(postion_matrix);
- within_seq_matrix_reward=[1,1,1,1,0,0,0,0;1,1,1,1,0,0,0,0;1,1,1,1,0,0,0,0;1,1,1,1,0,0,0,0;0,0,0,0,0,0,0,0;0,0,0,0,0,0,0,0;0,0,0,0,0,0,0,0;0,0,0,0,0,0,0,0]
- for i=1:8
- within_seq_matrix_reward(i,i)=0
- end
- within_seq_matrix_reward=squareform(within_seq_matrix_reward);
- within_seq_matrix_neutral=[0,0,0,0,0,0,0,0;0,0,0,0,0,0,0,0;0,0,0,0,0,0,0,0;0,0,0,0,0,0,0,0;0,0,0,0,1,1,1,1;0,0,0,0,1,1,1,1;0,0,0,0,1,1,1,1;0,0,0,0,1,1,1,1]
- for i=1:8
- within_seq_matrix_neutral(i,i)=0
- end
- within_seq_matrix_neutral=squareform(within_seq_matrix_neutral);
- cons1st1=ones(28,1);
- matrix=[postion_matrix' within_seq_matrix_reward' within_seq_matrix_neutral' cons1st1];
- distance_beta = nan(numberSubjects, 85, 1,4);
- for sub=1:numberSubjects
- for iT=1:85
- for iprem=1:1001
- y=squeeze(dRDM_new(sub,:,:,iT,iprem));
- y=squareform(y);
- bbb=pinv(matrix)*(y');
- distance_beta(sub,iT,iprem,:)=bbb;
- end
- end
- end
- save distance_beta.mat distance_beta
step01_RAS_main_code.m, under CC-BY-4.0 · at the source
Overview
- State Key Laboratory of Cognitive Neuroscience and Learning, IDG/McGovern Institute for Brain Research, Beijing Normal University,Beijing, China
- Chinese Institute for Brain Research,Beijing, China
- School of Psychology, Center for Brain Disorders and Cognitive Science, Shenzhen University,Shenzhen, China
- Center for Neurocognition and Social Behavior, Institute of Artificial Intelligence, Shenzhen University of Advanced Technology,Shenzhen, China
- Institute for Neuropsychological Rehabilitation, University of Health and Rehabilitation Sciences, Qingdao, China
- Max Planck University College London Centre for Computational Psychiatry and Ageing Research, Wellcome Centre for Human Neuroimaging, University College London,London, UK
- Department of Psychiatry, Universitätsmedizin Berlin,Berlin, Germany
- Department of Psychiatry, Wellcome Centre for Integrative Neuroimaging, University of Oxford,Oxford, UK
Abstract
The abstract is not reproduced here: the paper's license (none stated) does not allow it. Read it in the paper, at the publisher or on Europe PMC.
Repository
Its files are read in the Code ↔ Paper reader above, with 4 matches between paragraphs and lines of code.
Zenodo 15795242
Availability: 1 check, the latest on 26 September 2026: the link answers (HTTP 200)
- 26 September 2026: the link answers (HTTP 200)
14 files
- Decode_code.zip/
Decode_main_code.m , MATLAB, 113 lines - Decode_code.zip/
distinguishable_colors.m , MATLAB, 152 lines - Decode_code.zip/
plot_figure_3a.m , MATLAB, 61 lines - Decode_code.zip/
scaleFunc.m , MATLAB, 9 lines - Decode_code.zip/
shadedErrorBar.m , MATLAB, 160 lines - Decode_code.zip/
squash.m , MATLAB, 8 lines - Decode_code.zip/
uperms.m , MATLAB, 122 lines - RSA_code.zip/
covCor.m , MATLAB, 92 lines - RSA_code.zip/
shadedErrorBar.m , MATLAB, 160 lines - RSA_code.zip/
step01_RAS_main_code.m , MATLAB, 334 lines, 4 matches - RSA_code.zip/
step02_correction_for_su , MATLAB, 96 linesmR.m - RSA_code.zip/
step02_correction_for_su , MATLAB, 190 linesmT.m - RSA_code.zip/
step03_plot_figure5b.m , MATLAB, 78 lines - RSA_code.zip/
uperms.m , MATLAB, 122 lines
Code availability statement
The paper has a code availability statement. Its license (none stated) does not allow reproducing it here; in short, from what the harvester recognized in it:
- it points to the authors' code: Zenodo 15795242
Read it in the paper: doi.org/10.1038/s41467-025-63281-w.
Tracing map
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What the map holds:
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- 14 scripts, each with its path and the digest of its content;
- 4 matches between paragraphs of the paper and lines of the code (method lexical-v1);
- neither the text of the paper nor the code itself.
Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
Datasets cited
- zenodo:15792506, at Zenodo; found in “Data availability”
Data availability statement
The paper has a data availability statement. Its license (none stated) does not allow reproducing it here; in short, from what the harvester recognized in it:
- it points to a dataset: Zenodo 15792506
- it says that the data are available on request
Read it in the paper: doi.org/10.1038/s41467-025-63281-w.
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Version 3, 28 September 2026
- Funding: added National Natural Science Foundation of China: 32271093, 31920103009, ZD153; Shenzhen-Hong Kong Institute of Brain Science: (2022SHIBS0003; Fundamental Research Funds for the Central Universities; National Social Science Fund of China
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 9 authors, 3 keywords, 10 MeSH terms, 83 references.
Cite
This paper
Yu, Q., Luo, Y.-j., Dolan, R., Ou, J., Huang, C., Wang, H., Xiao, Z., Nour, M., & Liu, Y. (2025). Trait anxiety is associated with reduced reward-related replay at rest. Nature Communications, 16(1), 7975. https://
BibTeX
@article{yu2025trait,
author = {Yu, Qianqian and Luo, Yue-jia and Dolan, Ray and Ou, Jianxin and Huang, Chuwen and Wang, Haiteng and Xiao, Zhibing and Nour, Matthew and Liu, Yunzhe},
title = {{Trait anxiety is associated with reduced reward-related replay at rest}},
journal = {Nature Communications},
year = {2025},
volume = {16},
number = {1},
pages = {7975},
publisher = {Nature Publishing Group},
issn = {2041-1723},
doi = {10.1038/
url = {https://
pmcid = {PMC12381021}
}
RIS
TY - JOUR
AU - Yu, Qianqian
AU - Luo, Yue-jia
AU - Dolan, Ray
AU - Ou, Jianxin
AU - Huang, Chuwen
AU - Wang, Haiteng
AU - Xiao, Zhibing
AU - Nour, Matthew
AU - Liu, Yunzhe
TI - Trait anxiety is associated with reduced reward-related replay at rest
T2 - Nature Communications
J2 - Nat Commun
PY - 2025
DA - 2025
VL - 16
IS - 1
SP - 7975
SN - 2041-1723
PB - Nature Publishing Group
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
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"title": "Trait anxiety is associated with reduced reward-related replay at rest",
"container-title": "Nature Communications",
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{
"family": "Yu",
"given": "Qianqian"
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"given": "Yue-jia"
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{
"family": "Dolan",
"given": "Ray"
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{
"family": "Ou",
"given": "Jianxin"
},
{
"family": "Huang",
"given": "Chuwen"
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"given": "Yunzhe"
}
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"volume": "16",
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"page": "7975",
"DOI": "10.1038/
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"publisher": "Nature Publishing Group",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
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2025
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]
}
}
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