(A) Comparison of strength of CCA result for network matrices, spatial maps and amplitudes (node timeseries standard deviation) derived from several distinct group-average spatial parcellations/decompositions: ICA decompositions at two scales of detail (dimensionalities of 25 and 200, with ‘ICA200 partial network matrix’ corresponding to the measures used previously [Smith et al., 2015]); a PROFUMO decomposition (PFM; dimensionality 50); an atlas-based hard parcellation (108 parcels [Yeo et al., 2011]), task contrast spatial maps (86 contrasts, 47 unique), and warp field from native space to MSMAll alignment. Each bar reports a separate CCA analysis (first CCA mode shown), performed against behaviour/life-factors. A similar mode of variation is found across most of the parcellation methods and different fMRI measures. rUV is the strength of the canonical correlation between imaging and non-imaging measures. Error bars indicate confidence intervals (2.5–97.5%) estimated using surrogate data (generated with the same correlation structure), and red lines reflect the p<0.002 significant threshold compared with a null distribution obtained with permutation testing (i.e. family-wise-error corrected across all CCA components and Bonferroni corrected across a total of 25 CCAs performed, see Supplementary file 1a and b for the full set of results). CCA estimates the highest possible ruv given the dataset; therefore, the null distribution for low-dimensional brain data (e.g. ICA 25 amplitude) is expected to be lower than for high-dimensional brain data. (B) Set of non-imaging variables that correlate most strongly with the CCA mode (averaged subject weights V across results marked with * in A; i.e. p=0.00001) with behavioural variables. Position against the y-axis and font size indicate strength of correlation.
Figure 1—source data 1. Source data for Figure 1.