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coactivation.py
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coactivation.py
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from neurosynth.analysis.meta import MetaAnalysis
import nibabel as nib
import numpy as np
from copy import deepcopy
def mask_level(img, level):
img = deepcopy(img)
data = img.get_data()
data[:] = np.round(data)
data[data != level] = 0
data[data == level] = 1
return img
def coactivation_contrast(dataset, infile, regions=None, target_thresh=0.01,
other_thresh=0.01, q=0.01, contrast='others'):
""" Performs meta-analyses to contrast co-activation in a target region vs
co-activation of other regions. Contrasts every region in "regions" vs
the other regions in "regions"
dataset: Neurosynth dataset
infile: Nifti file with masks as levels
regions: which regions in image to contrast
target_thresh: activaton threshold for retrieving ids for target region
other_thresh: activation threshold for ids in other regions
stat: which image to return from meta-analyis. Default is usually correct
returns: a list of nifti images for each contrast performed of length = len(regions) """
if isinstance(infile, str):
image = nib.load(infile)
else:
image = infile
affine = image.get_affine()
stat="pFgA_z_FDR_%s" % str(q)
if regions == None:
regions = np.round(np.unique(infile.get_data()))[1:]
meta_analyses = []
for reg in regions:
if contrast == 'others':
other_ids = [dataset.get_studies(mask=mask_level(image, a), activation_threshold=other_thresh)
for a in regions if a != reg]
joined_ids = set()
for ids in other_ids:
joined_ids = joined_ids | set(ids)
joined_ids = list(joined_ids)
elif contrast == 'joint':
mask = nib.Nifti1Image((image.get_data() != 0).astype('int'), affine=image.get_affine())
joined_ids = dataset.get_studies(mask = mask, activation_threshold=other_thresh)
else:
joined_ids = None
reg_ids = dataset.get_studies(mask=mask_level(image, reg), activation_threshold=target_thresh)
meta_analyses.append(MetaAnalysis(dataset, reg_ids, ids2=joined_ids, q=q))
return [nib.nifti1.Nifti1Image(dataset.masker.unmask(
ma.images[stat]), affine, dataset.masker.get_header()) for ma in meta_analyses]