# ============================================================================ # # PUBLIC DOMAIN NOTICE # # National Institute on Deafness and Other Communication Disorders # # This software/database is a "United States Government Work" under the # terms of the United States Copyright Act. It was written as part of # the author's official duties as a United States Government employee and # thus cannot be copyrighted. This software/database is freely available # to the public for use. The NIDCD and the U.S. Government have not placed # any restriction on its use or reproduction. # # Although all reasonable efforts have been taken to ensure the accuracy # and reliability of the software and data, the NIDCD and the U.S. Government # do not and cannot warrant the performance or results that may be obtained # by using this software or data. The NIDCD and the U.S. Government disclaim # all warranties, express or implied, including warranties of performance, # merchantability or fitness for any particular purpose. # # Please cite the author in any work or product based on this material. # # ========================================================================== # *************************************************************************** # # Large-Scale Neural Modeling software (LSNM) # # Section on Brain Imaging and Modeling # Voice, Speech and Language Branch # National Institute on Deafness and Other Communication Disorders # National Institutes of Health # # This file (func_conn_syn_visual.py) was created on May 4, 2015. # # Based in part by Matlab scripts by Horwitz et al. # # Author: Antonio Ulloa # # Last updated by Antonio Ulloa on September 7 2015 # **************************************************************************/ # func_conn_syn_visual.py # # Calculate and plot functional connectivity (within-task time series correlation) # of IT with all other simulated brain areas, using the output # from visual DMS task (integrated synaptic activity) on a single subject. import numpy as np import matplotlib.pyplot as plt import matplotlib as mpl import pandas as pd # set matplotlib parameters to produce visually appealing plots mpl.style.use('ggplot') #def plot_corr(df): # '''Plots correlation matrix, taking a pandas DataFrame as input # ''' # # corr = df.corr() # plt.matshow(corr) # plt.xticks(range(len(corr.columns)), corr.columns); # plt.yticks(range(len(corr.columns)), corr.columns); # plt.colorbar() # what are the locations of relevant TVB nodes within TVB array? #v1_loc = 345 #v4_loc = 393 #it_loc = 413 #pf_loc = 74 # define the name of the input file where the synaptic activities are stored SYN_file = 'synaptic_in_ROI_test_ignore.npy' # define the name of the output file where the functional connectivity timeseries will be stored func_conn_dms_file = 'corr_syn_IT_vs_all_dms_test_ignore.npy' func_conn_ctl_file = 'corr_syn_IT_vs_all_ctl_test_ignore.npy' # define the length of both each trial and the whole experiment # in synaptic timesteps, as well as total number of trials experiment_length = 3960 trial_length = 110 number_of_trials = 36 # define intertrial interval duration in number of synaptic timesteps ITI_length = 20 # define an array with location of control trials, and another array # with location of task-related trials, relative to # an array that contains all trials (task-related trials included) # We will use this array to split the synaptic activity timeseries # into separate trials. control_trials = [3,4,5,9,10,11,15,16,17,21,22,23,27,28,29,33,34,35] dms_trials = [0,1,2,6,7,8,12,13,14,18,19,20,24,25,26,30,31,32] # open file that contains the synaptic activities syn = np.load(SYN_file) # extract synaptic activities for each ROI v1_syn = syn[0] v4_syn = syn[1] it_syn = syn[2] fs_syn = syn[3] d1_syn = syn[4] d2_syn = syn[5] fr_syn = syn[6] lit_syn= syn[7] # Gets rid of the control trials in the synaptic activity arrays, # by separating the task-related trials and concatenating them # together. Remember that each trial is a number of synaptic timesteps # long. # first, split the arrays into subarrays, each one containing a single trial it_subarrays = np.split(it_syn, number_of_trials) v1_subarrays = np.split(v1_syn, number_of_trials) v4_subarrays = np.split(v4_syn, number_of_trials) d1_subarrays = np.split(d1_syn, number_of_trials) d2_subarrays = np.split(d2_syn, number_of_trials) fs_subarrays = np.split(fs_syn, number_of_trials) fr_subarrays = np.split(fr_syn, number_of_trials) lit_subarrays= np.split(lit_syn,number_of_trials) # we get rid of the inter-trial interval for each and all trials # 1 second at the end of each trial. # 1 second = 20 synaptic timesteps #ITI_start = trial_length - ITI_length # Get rid of the ITI, located at the end of each trial #it_subarrays = np.delete(it_subarrays, np.arange(ITI_start,trial_length), axis=1) #v1_subarrays = np.delete(v1_subarrays, np.arange(ITI_start,trial_length), axis=1) #v4_subarrays = np.delete(v4_subarrays, np.arange(ITI_start,trial_length), axis=1) #d1_subarrays = np.delete(d1_subarrays, np.arange(ITI_start,trial_length), axis=1) #d2_subarrays = np.delete(d2_subarrays, np.arange(ITI_start,trial_length), axis=1) #fs_subarrays = np.delete(fs_subarrays, np.arange(ITI_start,trial_length), axis=1) #fr_subarrays = np.delete(fr_subarrays, np.arange(ITI_start,trial_length), axis=1) #it_subarrays = np.delete(it_subarrays, np.arange(0,ITI_length), axis=1) #v1_subarrays = np.delete(v1_subarrays, np.arange(0,ITI_length), axis=1) #v4_subarrays = np.delete(v4_subarrays, np.arange(0,ITI_length), axis=1) #d1_subarrays = np.delete(d1_subarrays, np.arange(0,ITI_length), axis=1) #d2_subarrays = np.delete(d2_subarrays, np.arange(0,ITI_length), axis=1) #fs_subarrays = np.delete(fs_subarrays, np.arange(0,ITI_length), axis=1) #fr_subarrays = np.delete(fr_subarrays, np.arange(0,ITI_length), axis=1) # now, get rid of the control trials... it_DMS_trials = np.delete(it_subarrays, control_trials, axis=0) v1_DMS_trials = np.delete(v1_subarrays, control_trials, axis=0) v4_DMS_trials = np.delete(v4_subarrays, control_trials, axis=0) d1_DMS_trials = np.delete(d1_subarrays, control_trials, axis=0) d2_DMS_trials = np.delete(d2_subarrays, control_trials, axis=0) fs_DMS_trials = np.delete(fs_subarrays, control_trials, axis=0) fr_DMS_trials = np.delete(fr_subarrays, control_trials, axis=0) lit_DMS_trials= np.delete(lit_subarrays,control_trials, axis=0) # ... and concatenate the task-related trials together it_DMS_trials_ts = np.concatenate(it_DMS_trials) v1_DMS_trials_ts = np.concatenate(v1_DMS_trials) v4_DMS_trials_ts = np.concatenate(v4_DMS_trials) d1_DMS_trials_ts = np.concatenate(d1_DMS_trials) d2_DMS_trials_ts = np.concatenate(d2_DMS_trials) fs_DMS_trials_ts = np.concatenate(fs_DMS_trials) fr_DMS_trials_ts = np.concatenate(fr_DMS_trials) lit_DMS_trials_ts= np.concatenate(lit_DMS_trials) # but also, get rid of the DMS task trials, to create arrays that contain only control trials it_control_trials = np.delete(it_subarrays, dms_trials, axis=0) v1_control_trials = np.delete(v1_subarrays, dms_trials, axis=0) v4_control_trials = np.delete(v4_subarrays, dms_trials, axis=0) d1_control_trials = np.delete(d1_subarrays, dms_trials, axis=0) d2_control_trials = np.delete(d2_subarrays, dms_trials, axis=0) fs_control_trials = np.delete(fs_subarrays, dms_trials, axis=0) fr_control_trials = np.delete(fr_subarrays, dms_trials, axis=0) lit_control_trials= np.delete(lit_subarrays,dms_trials, axis=0) # ... and concatenate the control task trials together it_control_trials_ts = np.concatenate(it_control_trials) v1_control_trials_ts = np.concatenate(v1_control_trials) v4_control_trials_ts = np.concatenate(v4_control_trials) d1_control_trials_ts = np.concatenate(d1_control_trials) d2_control_trials_ts = np.concatenate(d2_control_trials) fs_control_trials_ts = np.concatenate(fs_control_trials) fr_control_trials_ts = np.concatenate(fr_control_trials) lit_control_trials_ts= np.concatenate(lit_control_trials) ############ TMP BEGINS # put all of the time-series together in preparation forthe correlation analysis #dms_trials = np.array([it_DMS_trials_ts, v1_DMS_trials_ts, v4_DMS_trials_ts, # d1_DMS_trials_ts, d2_DMS_trials_ts, fs_DMS_trials_ts, # fr_DMS_trials_ts]) #ctl_trials = np.array([it_control_trials_ts, v1_control_trials_ts, v4_control_trials_ts, # d1_control_trials_ts, d2_control_trials_ts, fs_control_trials_ts, # fr_control_trials_ts]) # extract the length of the time-series #ts_length = it_DMS_trials_ts.size # convert to Pandas dataframe, using the transpose to convert to a format where the names # of the modules are the labels for each time-series #dms_ts = pd.DataFrame(dms_trials.T, # columns=np.array(['V1', 'V4', 'IT', 'D1', 'D2', 'FS', 'FR']), # index=list(range(ts_length)) ) #ctl_ts = pd.DataFrame(ctl_trials.T, # columns=np.array(['V1', 'V4', 'IT', 'D1', 'D2', 'FS', 'FR']), # index=list(range(ts_length)) ) #plot_corr(dms_ts) #plot_corr(ctl_ts) #plt.show() ############ TMP ENDS # now, convert DMS and control timeseries into pandas timeseries, so we can analyze it IT_dms_ts = pd.Series(it_DMS_trials_ts) V1_dms_ts = pd.Series(v1_DMS_trials_ts) V4_dms_ts = pd.Series(v4_DMS_trials_ts) D1_dms_ts = pd.Series(d1_DMS_trials_ts) D2_dms_ts = pd.Series(d2_DMS_trials_ts) FS_dms_ts = pd.Series(fs_DMS_trials_ts) FR_dms_ts = pd.Series(fr_DMS_trials_ts) LIT_dms_ts= pd.Series(lit_DMS_trials_ts) IT_ctl_ts = pd.Series(it_control_trials_ts) V1_ctl_ts = pd.Series(v1_control_trials_ts) V4_ctl_ts = pd.Series(v4_control_trials_ts) D1_ctl_ts = pd.Series(d1_control_trials_ts) D2_ctl_ts = pd.Series(d2_control_trials_ts) FS_ctl_ts = pd.Series(fs_control_trials_ts) FR_ctl_ts = pd.Series(fr_control_trials_ts) LIT_ctl_ts= pd.Series(lit_control_trials_ts) # ... and calculate the functional connectivity of IT with the other modules, # using the Pearson correlation coefficient funct_conn_it_v1_dms = IT_dms_ts.corr(V1_dms_ts, method='pearson') funct_conn_it_v4_dms = IT_dms_ts.corr(V4_dms_ts, method='pearson') funct_conn_it_d1_dms = IT_dms_ts.corr(D1_dms_ts, method='pearson') funct_conn_it_d2_dms = IT_dms_ts.corr(D2_dms_ts, method='pearson') funct_conn_it_fs_dms = IT_dms_ts.corr(FS_dms_ts, method='pearson') funct_conn_it_fr_dms = IT_dms_ts.corr(FR_dms_ts, method='pearson') funct_conn_it_lit_dms= IT_dms_ts.corr(LIT_dms_ts,method='pearson') funct_conn_it_v1_ctl = IT_ctl_ts.corr(V1_ctl_ts, method='pearson') funct_conn_it_v4_ctl = IT_ctl_ts.corr(V4_ctl_ts, method='pearson') funct_conn_it_d1_ctl = IT_ctl_ts.corr(D1_ctl_ts, method='pearson') funct_conn_it_d2_ctl = IT_ctl_ts.corr(D2_ctl_ts, method='pearson') funct_conn_it_fs_ctl = IT_ctl_ts.corr(FS_ctl_ts, method='pearson') funct_conn_it_fr_ctl = IT_ctl_ts.corr(FR_ctl_ts, method='pearson') funct_conn_it_lit_ctl= IT_ctl_ts.corr(LIT_ctl_ts,method='pearson') # pack correlation coefficients in preparation for saving to a file func_conn_dms = np.array([funct_conn_it_v1_dms,funct_conn_it_v4_dms, funct_conn_it_fs_dms,funct_conn_it_d1_dms, funct_conn_it_d2_dms,funct_conn_it_fr_dms, funct_conn_it_lit_dms]) func_conn_ctl = np.array([funct_conn_it_v1_ctl,funct_conn_it_v4_ctl, funct_conn_it_fs_ctl,funct_conn_it_d1_ctl, funct_conn_it_d2_ctl,funct_conn_it_fr_ctl, funct_conn_it_lit_ctl]) # now, save all correlation coefficients to a output files np.save(func_conn_dms_file, func_conn_dms) np.save(func_conn_ctl_file, func_conn_ctl) # define number of groups to plot N = 2 # create a list of x locations for each group index = np.arange(N) width = 0.1 # width of the bars fig, ax = plt.subplots() ax.set_ylim([-0.2,1]) # now, group the values to be plotted by brain module it_v1_corr = (funct_conn_it_v1_dms, funct_conn_it_v1_ctl) it_v4_corr = (funct_conn_it_v4_dms, funct_conn_it_v4_ctl) it_fs_corr = (funct_conn_it_fs_dms, funct_conn_it_fs_ctl) it_d1_corr = (funct_conn_it_d1_dms, funct_conn_it_d1_ctl) it_d2_corr = (funct_conn_it_d2_dms, funct_conn_it_d2_ctl) it_fr_corr = (funct_conn_it_fr_dms, funct_conn_it_fr_ctl) it_lit_corr= (funct_conn_it_lit_dms,funct_conn_it_lit_ctl) rects_v1 = ax.bar(index, it_v1_corr, width, color='yellow', label='V1') rects_v4 = ax.bar(index + width, it_v4_corr, width, color='green', label='V4') rects_fs = ax.bar(index + width*2, it_fs_corr, width, color='orange', label='FS') rects_d1 = ax.bar(index + width*3, it_d1_corr, width, color='red', label='D1') rects_d2 = ax.bar(index + width*4, it_d2_corr, width, color='pink', label='D2') rects_fr = ax.bar(index + width*5, it_fr_corr, width, color='purple', label='FR') rects_lit= ax.bar(index + width*6, it_lit_corr, width, color='lightblue', label='cIT') #ax.set_title('FUNCTIONAL CONNECTIVITY OF IT WITH ALL OTHER BRAIN REGIONS') # get rid of x axis ticks and labels ax.set_xticks([]) ax.set_xlabel('DMS TASK CONTROL TASK') ax.xaxis.set_label_coords(0.5, -0.025) ax.set_ylabel('r-value') # Shrink current axis by 10% to make space for legend box = ax.get_position() ax.set_position([box.x0, box.y0, box.width * 0.9, box.height]) # place a legend to the right of the figure plt.legend(loc='center left', bbox_to_anchor=(1.02, .5)) # Show the plots on the screen plt.show()