def __init__(self, path, *, dtype=None, dpi=None, sid=None):
"""
Parameters
----------
path : str, file-object
The path to the file or the data stream.
dtype : dtype, None, optional
The data type to cast the image data as. If None, will use whatever raw image format is.
dpi : int, float
The dots-per-inch of the image, defined at isocenter.
.. note:: If a DPI tag is found in the image, that value will override the parameter, otherwise this one
will be used.
sid : int, float
The Source-to-Image distance in mm.
"""
super().__init__(path)
self._sid = sid
self._dpi = dpi
# read the file once to get just the DICOM metadata
self.metadata = dicom.read_file(path, force=True)
self._original_dtype = self.metadata.pixel_array.dtype
# read a second time to get pixel data
if isinstance(path, BytesIO):
path.seek(0)
ds = dicom.read_file(path, force=True)
if dtype is not None:
self.array = ds.pixel_array.astype(dtype)
else:
self.array = ds.pixel_array
# convert values to proper HU: real_values = slope * raw + intercept
if self.metadata.SOPClassUID.name == 'CT Image Storage':
self.array = int(self.metadata.RescaleSlope)*self.array + int(self.metadata.RescaleIntercept)
def main():
dcm = dicom.read_file(sys.argv[1])
img=dcm.pixel_array
sg = SkeletonGraph(img)
arg2 = dicom.read_file(sys.argv[2])
img2 = arg2.pixel_array
sg.setOriginalImage(img2)
#sg.setOriginalImage(fname=sys.argv[2])
sg.getGraphsFromSkeleton(verbose=False)
sg.setLargestGraphToCurrentGraph()
list(sg.graphs.keys())
sg.findEndpointsBifurcations()
root = sg.selectSeedFromDFE()
#sg.viewGraph()
#raw_input('continue')
sg.setRoot(root,key="test")
sg.traceEndpoints(key='test')
ogkey = sg.getLargestOrderedGraphKey()
sg.deleteDegree2Nodes(ogkey)
sg.prunePaths(ogkey)
sg.deleteDegree2Nodes(ogkey)
sg.fitEdges(key=ogkey)
og = sg.orderedGraphs[ogkey]
sg.viewGraph(og)
sg.saveGraphs(sys.argv[3])
def getDicomInfo(directory):
'''
Input : directory location
Output : dicom information
'''
#Looping through the input directory
switch='non-break'
firstDicomFile=''
for root, dirs, files in os.walk(directory):
#Looping through the bunch of files
for singleFile in files:
#if there is dicom files
if re.search('.*ima|.*dcm|\d{8}',singleFile,flags=re.IGNORECASE):
try:
firstDicomFile = dicom.read_file(os.path.join(root,singleFile))
except:
firstDicomFile = dicom.read_file(os.path.join(root,singleFile),force=True)
#make a switch to turn off the later loops
switch='break'
#turn the file loop off
break
else:
switch='non-break'
#if switch is on, turn the dir loop off
if switch=='break':
break
return firstDicomFile
def get_blur(df_s, path):
df_s = remove_weird_slice(df_s)
Dset = []
for idx in range(len(df_s)):
#Get brightest and darkest frames for study number idx
#idx = 0
ext = df_s.index[idx]
#print ext
BT = np.argmax(df_s['brightness'][idx])
DK = np.argmin(df_s['brightness'][idx])
filename1 = os.listdir(path + '/' + ext)[BT]
filename2 = os.listdir(path + '/' + ext)[DK]
dcm1 = path + '/' + ext+ '/' + filename1
dcm2 = path + '/' + ext+ '/' + filename2
ds1 = dicom.read_file(dcm1)
ds2 = dicom.read_file(dcm2)
data1 = ds1.pixel_array
data2 = ds2.pixel_array
# plt.imshow(data1, cmap=plt.cm.bone)
# plt.show()
# plt.imshow(data2, cmap=plt.cm.bone)
# plt.show()
datab1 = cv2.blur(data1,(7,7))
datab2 = cv2.blur(data2,(7,7))
#D is delta between brightest and darkest image for a slice
D = abs(datab2.astype(int) - datab1.astype(int))
Dset.append(D)
#plt.imshow(D, cmap=plt.cm.bone)
#plt.show()
#Average deltas for all slices gives region of movement
return np.mean(np.array(Dset), axis = 0)
def times(self):
"""
Determines the time of each series. 'time' is a string.
"""
types=self.type
process=self.processed
os.chdir(data_loc)
if process:
time='Processed'
else:
if types=='T1 Dynamic':
original=dicom.read_file(self.filename)
time1=original.ContentTime
time2=original.ContentTime
#still has to go through entire hard drive
files=os.listdir(data_loc)
for i in files:
data=dicom.read_file(i)
if data.SeriesInstanceUID==original.SeriesInstanceUID:
if data.ContentTime<time1:
time1=data.ContentTime
elif data.ContentTime>time2:
time2=data.ContentTime
else:
pass
else:
pass
time=str(time1)+'-'+str(time2)
else:
time=None
self.time=time
return
def __load_pydicom(image):
"""
Image loader using the third-party module pydicom.
@param image the image to load
@return A tuple of 1. a scipy array with the image data, 2. a ImageHeader object with additional information
"""
import dicom
logger = Logger.getInstance()
logger.debug('Loading image {} with PyDicom...'.format(image))
try:
img = dicom.read_file(image)
except dicom.filereader.InvalidDicomError as e:
logger.debug('Module pydicom signaled error: {}. Attempting to force loading nevertheless'.format(e))
img = dicom.read_file(image, force=True)
arr = img.pixel_array
# Dicom images are difficult and require special treatment:
# (1) Usually, when saved as DICOM image, row and solumn direction as exchanged as
# compared to other image modailites.
# (2) Furthermore PyDicom loads DICOM images with the 3rd dimension (Frames/Slices)
# in the first numpy ndarray position.
# Thus, to ensure consistency between the loaded data independent of the 3rd party
# tool or image format used, we have to
# (a) transpose the data array, which counters both, point (1) and point (2) in one go
# (b) flip the first and second (column and row) element of the pixel spacing
# Note: Strangely the offset i.e. PatientPosition does not have do be flipped... why?
pixel_spacing = scipy.asarray(header.get_pixel_spacing(img))
tmp = float(pixel_spacing[1])
pixel_spacing[1] = pixel_spacing[0]
pixel_spacing[0] = tmp
header.set_pixel_spacing(img, pixel_spacing)
return scipy.transpose(arr), img
def __init__(self, **kwargs):
med2image.__init__(self, **kwargs)
self.l_dcmFileNames = sorted(glob.glob('%s/*.dcm' % self._str_inputDir))
self.slices = len(self.l_dcmFileNames)
if self._b_convertMiddleSlice:
self._sliceToConvert = int(self.slices/2)
self._dcm = dicom.read_file(self.l_dcmFileNames[self._sliceToConvert])
self._str_inputFile = self.l_dcmFileNames[self._sliceToConvert]
str_outputFile = self.l_dcmFileNames[self._sliceToConvert]
if not self._str_outputFileStem.startswith('%'):
self._str_outputFileStem, ext = os.path.splitext(self.l_dcmFileNames[self._sliceToConvert])
if not self._b_convertMiddleSlice and self._sliceToConvert != -1:
self._dcm = dicom.read_file(self.l_dcmFileNames[self._sliceToConvert])
else:
self._dcm = dicom.read_file(self._str_inputFile)
if self._sliceToConvert == -1:
self._b_3D = True
self._dcm = dicom.read_file(self._str_inputFile)
image = self._dcm.pixel_array
shape2D = image.shape
#print(shape2D)
self._Vnp_3DVol = np.empty( (shape2D[0], shape2D[1], self.slices) )
i = 0
for img in self.l_dcmFileNames:
self._dcm = dicom.read_file(img)
image = self._dcm.pixel_array
#print('%s: %s\n' % (img, image.shape))
try:
self._Vnp_3DVol[:,:,i] = image
except Exception, e:
error.fatal(self, 'dcmInsertionFail', '\nFor input DICOM file %s\n%s\n' % (img, str(e)))
i += 1
def getDicomInfoAuto(firstDicomAddress):
try:
df = dicom.read_file(firstDicomAddress)
dob = df.PatientBirthDate
sex = df.PatientSex
pID = df.PatientID
date = df.StudyDate
age,dob,date=calculate_age(dob,date)
name = df.PatientName
print name
print dob
print sex
print pID
print date
print age
return {'name':name,
'dob':dob,
'sex':sex,
'patientId':pID,
'scanDate':date,
'age':age,
'dicomRead':df}
except:
dicom.read_file(firstDicomAddress,force=True)
print 'cannot properly read dicom file'
def get_images(self):
#Read images in from the same folder
imfilenames=glob.glob(os.path.join(self.contourdirectory,'*MR*'))
IPP=[dicom.read_file(x).ImagePositionPatient for x in imfilenames]
IPPz=[f[2] for f in IPP]
together=zip(IPPz,imfilenames,IPP)
together=sorted(together)
sortedimfilenames=[y[1] for y in together]
sortedUIDfromimfilenames=[x.split('MR.')[1] for x in sortedimfilenames]
sortedIPP=[z[2] for z in together]
sortedIPPz=[p[0] for p in together]
#Read in the files in the proper order
#Read in first one to get information needed
info=dicom.read_file(sortedimfilenames[0])
cols=info.Columns
rows=info.Rows
PS=info.PixelSpacing
im=info.pixel_array
images=np.zeros(np.array([im.shape[0],im.shape[1],len(sortedimfilenames)]))
for i in range(0,len(sortedimfilenames)):
temp=dicom.read_file(sortedimfilenames[i])
images[:,:,i]=temp.pixel_array
self.images=images
self.sortedIPP=sortedIPP
self.sortedUIDfromimfilenames=sortedUIDfromimfilenames
self.rows=rows
self.cols=cols
self.PS=PS
def _read_all_dicom_images(self):
f1 = self._filename(self.slices[0], self.time[0])
d1 = dicom.read_file(f1)
(x, y) = d1.PixelSpacing
(x, y) = (float(x), float(y))
if len(self.slices)>1:
f2 = self._filename(self.slices[1], self.time[0])
d2 = dicom.read_file(f2)
# try a couple of things to measure distance between slices
try:
if len(self.slices)>1:
dist = np.abs(d2.SliceLocation - d1.SliceLocation)
else:
dist = d1.SliceThickness
except AttributeError:
try:
dist = d1.SliceThickness
except AttributeError:
dist = 8 # better than nothing...
self.images = np.array([[self._read_dicom_image(self._filename(d, i))
for i in self.time]
for d in self.slices])
self.dist = dist
self.area_multiplier = x * y
def read_structural(self,seriestag): #method to read image stack - read in by file name due to poor dicom conversion
# Find folder that matches seriestag
stackfolder=glob.glob(os.path.join(self.datadirect,seriestag))
if not stackfolder:
print('Folder not found')
return
print('Found ', stackfolder[0])
# find .dcm files
filenames=glob.glob(os.path.join(stackfolder[0],'*.dcm'))
print('Check file ordering: ')
for item in filenames:
print(os.path.split(item)[1])
numfiles=len(filenames)
print("Reading "+str(numfiles)+" files")
# read the first file to find out size, and add pixel size info to T2winfo structure
info=dicom.read_file(filenames[0])
self.structuralinfo=np.zeros(1,dtype=[('pixelsize','f8')])
self.structuralinfo['pixelsize']=float(info.PixelSpacing[0])
im=info.pixel_array
ims=np.zeros(np.array([im.shape[0],im.shape[1],numfiles]))
for i in range(0,numfiles):
temp=dicom.read_file(filenames[i])
ims[:,:,i]=np.flipud(temp.pixel_array)
self.structural=ims
def __init__(self, paths,typeFloat):
''' Initialization
'''
self._dicomReaders = []
self._typeFloat = typeFloat
for path in paths:
if os.path.isdir(path):
for infile in glob.glob( os.path.join(path, '*.dcm') ):
dicomFile = dicom.read_file(infile)
dcmFileType = str(dicomFile.SOPClassUID)
if dcmFileType == 'CT Image Storage':
reader = DicomCTReader(path,typeFloat)
break
else:
raise ValueError("Directory: Case not defined yet in dicom reader")
else:
dicomFile = dicom.read_file(path)
dcmFileType = str(dicomFile.SOPClassUID)
if dcmFileType == 'RT Dose Storage':
reader = DicomRDReader(path,typeFloat)
elif dcmFileType == 'RT Ion Plan Storage':
reader = DicomRPReader(path,typeFloat)
elif dcmFileType == 'RT Structure Set Storage':
reader = DicomRSReader(path,typeFloat)
else:
reader = DicomGeneralReader(path,typeFloat)
self._dicomReaders.append(reader)
self._fullPlan = self.checkFullRTPlan()
print "Full RT Plan (CT, RP, RD, RS): %s"%str(self._fullPlan)
self._sameFrameOfRefUID = self.checkFrameOfReferenceUID()
print "Same Frame Of Reference UID: %s"%str(self._sameFrameOfRefUID)
self._sameStudyInstanceUID = self.checkSameStudyInstanceUID()
print "Same Study Instance UID: %s"%str(self._sameStudyInstanceUID)
def _read_all_dicom_images(self):
#Computing distance between...
f1 = self._filename(self.slices[0], self.time[0])
d1 = dicom.read_file(f1)
(x, y) = d1.PixelSpacing
(x, y) = (float(x), float(y))
f2 = self._filename(self.slices[1], self.time[0])
d2 = dicom.read_file(f2)
# try a couple of things to measure distance between slices
try:
dist = np.abs(d2.SliceLocation - d1.SliceLocation)
except AttributeError:
try:
dist = d1.SliceThickness
except AttributeError:
dist = 8 # better than nothing...
self.images = np.array([[self._read_dicom_image(self._filename(d, i))
for i in self.time]
for d in self.slices])
# sets dist equal to the two first slices distance (subtracting first
# from second) or equal to first slice's thickness. I THINK the second
# logic is better
#
# maybe set dist = d1.SliceThickness
self.dist = dist
self.area_multiplier = x * y
def find_files(self, base_dir):
'''
When we run the deident software we won't know the name of the
directory the image gets put into; however it will (should!) be
the only subdirectory present in the specified output directory,
and we just need to get its name
'''
# Find the directories that the de-ident software created
dirnames = os.listdir(base_dir)
# Now find the dicom files inside each directory
dicom_files = []
for directory in dirnames:
files = os.listdir(os.path.join(base_dir, directory))
# now see which are dicom images
for f in files:
try:
file_path = os.path.join(base_dir, directory, f)
dicom.read_file(os.path.join(file_path))
dicom_files.append(file_path)
except Exception as msg:
sys.stdout.write("Warning: Found invalid DICOM file: %s\n"
% os.path.join(base_dir, directory, f))
if len(dicom_files) == 0:
sys.stdout.write("ERROR: No Dicom images found at: %s\n"
% os.path.join(base_dir, directory))
return 0
return dicom_files
def ReadDicom(dicom_dir='dicom', points_threshold=1100):
# Get the dicom file list.
files = sorted(glob.glob(os.path.join(dicom_dir, 'CT*')))
# Get CT meta data.
data = dicom.read_file(files[0])
dims = (int(data.Rows), int(data.Columns), len(files))
# spacing is in mm.
spaces = (float(data.PixelSpacing[0]), float(data.PixelSpacing[1]), float(data.SliceThickness))
# Allocate spaces, loop through all the DICOM files
v = np.zeros(dims, dtype=data.pixel_array.dtype)
for f in files:
data = dicom.read_file(f)
v[:, :, files.index(f)] = data.pixel_array
# Get 3 dimension data. Use t as the filter.
t = v >= points_threshold
a = t.nonzero()
v = v[t]
v = v.reshape(len(a[0]))
data = np.array([a[0] * spaces[0], a[1] * spaces[1], a[2] * spaces[2], v])
# Return a ? * 4 matrix
data = data.transpose()
return data
def read_dicom(path):
import re
files = []
arr = None
for dirName, subdirList, fileList in os.walk(path):
for filename in fileList:
m = re.search(r'IM\d+', filename)
if m <> None:
if filename[m.end(): ] == '':
files.append(os.path.join(dirName, filename))
if len(files) != 0:
reference = dicom.read_file(files[0])
height = int(reference.Rows)
width = int(reference.Columns)
slice_num = int(len(files))
spacing = (float(reference.PixelSpacing[0]),float(reference.PixelSpacing[1]), float(reference.SliceThickness))
# x = np.arange(0.0, (height*spacing[0], spacing[0]))
# y = np.arange(0.0, (width * spacing[1], spacing[1]))
# z = np.arange(0.0, (slice_num * spacing[2]), spacing[2])
arr = np.zeros((slice_num, height, width), dtype=np.int16)
for filename in files:
ds = dicom.read_file(filename)
arr[files.index(filename), :, : ] = ds.pixel_array
else:
import sys
sys.stderr.write("didn't find any images")
return arr
def is_dicom_dir(datapath):
"""
Check if in dir is one or more dicom file. We use two methods.
First is based on dcm extension detection.
"""
# Second tries open files
# with dicom module.
retval = False
for f in os.listdir(datapath):
if f.endswith((".dcm", ".DCM")):
retval = True
return True
# @todo not working and I dont know why
try:
dicom.read_file(f)
retval = True
except:
import traceback
traceback.print_exc
pass
if retval:
return True
print f
return False
def genepara(namedirtopcf):
dirFileP = os.path.join(namedirtopcf, source)
listsln=[]
#list dcm files
fileList =[name for name in os.listdir(dirFileP) if ".dcm" in name.lower()]
slnt=0
for filename in fileList:
FilesDCM =(os.path.join(dirFileP,filename))
RefDs = dicom.read_file(FilesDCM,force=True)
scanNumber=int(RefDs.InstanceNumber)
if scanNumber>slnt:
slnt=scanNumber
listsln.append(scanNumber)
FilesDCM =(os.path.join(dirFileP,fileList[0]))
FilesDCM1 =(os.path.join(dirFileP,fileList[1]))
RefDs = dicom.read_file(FilesDCM,force=True)
RefDs1 = dicom.read_file(FilesDCM1,force=True)
patientPosition=RefDs.PatientPosition
# SliceThickness=RefDs.SliceThickness
try:
slicepitch = np.abs(RefDs.ImagePositionPatient[2] - RefDs1.ImagePositionPatient[2])
except:
slicepitch = np.abs(RefDs.SliceLocation - RefDs1.SliceLocation)
SliceThickness=RefDs.SliceThickness
try:
SliceSpacingB=RefDs.SpacingBetweenSlices
except AttributeError:
print "Oops! No Slice spacing..."
SliceSpacingB=0
print 'number of slices', slnt
print 'slice Thickness :',SliceThickness
print 'Slice spacing',SliceSpacingB
print 'slice pitch in z :',slicepitch
print 'patient position :',patientPosition
errorfile = open(eferror, 'a')
errorfile.write('---------------\n')
errorfile.write('number of slices :'+str(slnt)+'\n')
errorfile.write('slice Thickness :'+str(SliceThickness)+'\n')
errorfile.write('slice spacing :'+str(SliceSpacingB)+'\n')
errorfile.write('slice pitch in z :'+str(slicepitch)+'\n')
errorfile.write('patient position :'+str(patientPosition)+'\n')
slnt=slnt+1
fxs=float(RefDs.PixelSpacing[0])/avgPixelSpacing
dsr= RefDs.pixel_array
dsr= dsr-dsr.min()
dsr=dsr.astype('uint16')
errorfile.write('patient shape :'+str(dsr.shape[0])+'\n')
errorfile.write('--------------------------------\n')
errorfile.close()
# dsrresize = scipy.ndimage.interpolation.zoom(dsr, fxs, mode='nearest')
# dsrresize=cv2.resize(dsr,None,fx=fxs,fy=fxs,interpolation=cv2.INTER_CUBIC)
dimtabx=dimtabxref
dimtaby=dimtabxref
return dimtabx,dimtaby,slnt,fxs,listsln
def isValidDcmFile(self, fileName):
valid = False;
try:
dicom.read_file(fileName)
valid = True;
except:
valid = False;
return valid;
def main():
print("Creating data iterator...")
with open("config.yml", 'r') as ymlfile:
cfg = yaml.load(ymlfile)
train_dir = cfg['dataset_paths']['train_data']
train_labels = cfg['dataset_paths']['train_labels']
mri_iter = MRIDataIterator(train_dir, train_labels)
outputdir = './testpreproc/'
for patient_index, patient_slices in mri_iter.frames.iteritems():
slices_locations_to_names = {}
i = 0
for sax_set in patient_slices:
slices_locations_to_names[int(dicom.read_file(sax_set[0]).SliceLocation)] = i
i += 1
median_array = slices_locations_to_names.keys()
median_array.sort()
values_closest_to_middle = []
if len(median_array) > 1:
middle_value = (median_array[-1] + median_array[0])/2
for val in median_array:
if math.sqrt((val - middle_value)**2) < 25:
values_closest_to_middle.append(val)
else:
middle_value = median_array[0]
values_closest_to_middle.append(median_array[0])
z = 0
values = []
for proposed_median_value in values_closest_to_middle:
median_index = slices_locations_to_names[proposed_median_value]
sax_set = patient_slices[median_index]
time_series = []
for path in sax_set:
f = dicom.read_file(path)
gender = f.PatientsSex
age = convert_age(f.PatientsAge)
img = mri_iter.preproc(f.pixel_array.astype(np.float32) / np.max(f.pixel_array), 64, f.PixelSpacing, True, False)
time_series.append(img)
values.append(time_series)
z +=1
data_array = np.array(values)
rois,circles = calc_rois(data_array)
i = 0
import pdb; pdb.set_trace()
new_set = []
for sax_set in data_array:
center_point, radius = circles[i]
new_time_series = []
for img in sax_set:
# make it square
crop_img = img[center_point[0]-40:center_point[0]+40, center_point[1]-60:center_point[1]+20]
new_time_series.append(crop_img)
new_set.append(new_time_series)
new_data_array = np.array(new_set)
im = Image.fromarray(new_data_array[0][0]).convert('RGB')
im.save('examples/' + randword() +'.png')
def convert_nifti_2_dicoms(nifti_path, dicom_targets, dicom_source,
output_folder, label=None):
"""Convert 4D niftis generated by reg_f3d into DICOM files.
:param nifti_path: path to the nifti file
:param dicom_target: list of dicom files from the target
for the registration for header info
:param dicom_source: one dicom file from the source
for the registration for header info
:param output_folder: folder where the DICOM files will be saved
:param label: name for the output dicom files
:return: None
"""
if not os.path.isfile(nifti_path):
raise Exception("NIFTI File %s not found." % nifti_path)
# Load image from NIFTI
f_img = nib.load(nifti_path)
f_img_data = f_img.get_data()
# Load dicom headers
if not os.path.isfile(dicom_source):
raise Exception("DICOM File %s not found ." % dicom_source)
adc_dcm_obj = dicom.read_file(dicom_source)
# Make output_folder:
if not os.path.exists(output_folder):
os.makedirs(output_folder)
# Series Number and SOP UID
ti = time.time()
series_number = 86532 + int(str(ti)[2:4]) + int(str(ti)[4:6])
sop_id = adc_dcm_obj.SOPInstanceUID.split('.')
sop_id = '.'.join(sop_id[:-1])+'.'
# Sort the DICOM T2 to create the ADC registered DICOMs
dcm_obj_sorted = dict()
for dcm_file in dicom_targets:
# Load dicom headers
if not os.path.isfile(dcm_file):
raise Exception("DICOM File %s not found." % dcm_file)
t2_dcm_obj = dicom.read_file(dcm_file)
dcm_obj_sorted[t2_dcm_obj.InstanceNumber] = t2_dcm_obj
for vol_i in range(f_img_data.shape[2]):
if f_img_data.shape[2] > 100:
filename = os.path.join(output_folder, '%s_%03d.dcm' % (label,
vol_i+1))
elif f_img_data.shape[2] > 10:
filename = os.path.join(output_folder, '%s_%02d.dcm' % (label,
vol_i+1))
else:
filename = os.path.join(output_folder, '%s_%d.dcm' % (label,
vol_i+1))
write_dicom(np.rot90(f_img_data[:, :, vol_i]), filename,
dcm_obj_sorted[vol_i+1], adc_dcm_obj, vol_i,
series_number, sop_id)
def genebmp(dirName,fn,subs):
"""generate patches from dicom files"""
# print ('load dicom files in :',dirName, 'scan name:',fn)
#directory for patches
predictout_f_dir = os.path.join( dirName,picklefile)
remove_folder(predictout_f_dir)
os.mkdir(predictout_f_dir)
# print 'predictoutdir', predictout_f_dir
subfile=os.path.join(predictout_f_dir,subsamplef)
subfilec = open(subfile, 'w')
subfilec.write('subsample '+str(subs)+'\n' )
subfilec.close()
bmp_dir = os.path.join(dirName, scanbmp)
FilesDCM =(os.path.join(dirName,fn))
#
ds = dicom.read_file(FilesDCM)
endnumslice=fn.find('.dcm')
imgcore=fn[0:endnumslice]+'.'+typei
posend=endnumslice
while fn.find('-',posend)==-1:
posend-=1
debnumslice=posend+1
slicenumber=int(fn[debnumslice:endnumslice])
bmpfile=os.path.join(bmp_dir,imgcore)
scipy.misc.imsave(bmpfile, ds.pixel_array)
lung_dir = os.path.join(dirName, lungmask)
lung_bmp_dir = os.path.join(lung_dir,lungmaskbmp)
lunglist = os.listdir(lung_dir)
# print(lung_bmp_dir)
# lungFound=False
for lungfile in lunglist:
# print(lungfile)
if ".dcm" in lungfile.lower():
endnumslice=lungfile.find('.dcm')
imgcorescan=lungfile[0:endnumslice]+'.'+typei
posend=endnumslice
while lungfile.find('_',posend)==-1:
posend-=1
debnumslice=posend+1
slicescan=int(lungfile[debnumslice:endnumslice])
# print slicescan
if slicescan== slicenumber:
# check whether the file's DICOM
lungDCM =os.path.join(lung_dir,lungfile)
dslung = dicom.read_file(lungDCM)
lungcore=imgcorescan+'.'+typei
lungcoref=os.path.join(lung_bmp_dir,lungcore)
scipy.misc.imsave(lungcoref, dslung.pixel_array)
break
def load_dicoms(self):
if os.path.isfile(self.filepath) and tarfile.is_tarfile(self.filepath): # compressed tarball
with tarfile.open(self.filepath) as archive:
self.dcm_list = [dicom.read_file(cStringIO.StringIO(archive.extractfile(ti).read())) for ti in archive if ti.isreg()]
elif os.path.isfile(self.filepath): # single file
self.dcm_list = [dicom.read_file(self.filepath)]
else: # directory of dicoms
self.dcm_list = [dicom.read_file(os.path.join(self.filepath, f)) for f in os.listdir(self.filepath)]
self.dcm_list.sort(key=lambda dcm: dcm.InstanceNumber)
def read_MOLLI(self,seriestag,PreOrPost): #Method to read in single slice MOLLI images, by filename due to poor dicom conversion
#Look for MOLLIpre and MOLLIpost.npy in the Analysis folder first
if PreOrPost=='Pre' and os.path.isfile(os.path.join(os.path.split(self.datadirect)[0],'Analysis','MOLLIpre.npy')):
print('reading from saved array')
self.MOLLIpre=np.load(os.path.join(os.path.split(self.datadirect)[0],'Analysis','MOLLIpre.npy'))
#self.dyninfo=np.load(os.path.join(os.path.split(self.datadirect)[0],'Analysis','dyninfo.npy'))
return
if PreOrPost=='Post' and os.path.isfile(os.path.join(os.path.split(self.datadirect)[0],'Analysis','MOLLIpost.npy')):
print('reading from saved array')
self.MOLLIpost=np.load(os.path.join(os.path.split(self.datadirect)[0],'Analysis','MOLLIpost.npy'))
#self.dyninfo=np.load(os.path.join(os.path.split(self.datadirect)[0],'Analysis','dyninfo.npy'))
# Use known series tag by calling disp_seriesfolders first
# Find folder that matches seriestag
MOLLIFolder=glob.glob(os.path.join(self.datadirect,seriestag))
if not MOLLIFolder:
print('Folder not found')
return
print('Found ',MOLLIFolder[0])
# Find all the filenames
MOLLIfiles=glob.glob(os.path.join(self.datadirect,MOLLIFolder[0],'*.dcm'))
numfiles=len(MOLLIfiles)
print("Reading "+str(numfiles)+" MOLLI files")
# Read the last file to work out size, check for manufacturer and fill out info variables
info=dicom.read_file(MOLLIfiles[-1])
im=info.pixel_array
# Find pixel sizes and other required dynamic info
# self.dyninfo=np.zeros(1,dtype=[('pixelsize','f8'),('TR','f8'),('FlipAngle','f8'),('tres','f8'),('numtimepoints','i4'),('numslices','i4')])
# self.dyninfo['pixelsize']=float(info.PixelSpacing[0])
# self.dyninfo['TR']=float(info.RepetitionTime)
# self.dyninfo['FlipAngle']=float(info.FlipAngle)
# Make an array to hold the dynamic data
MOLLIims=np.zeros((im.shape[0],im.shape[1],numfiles),dtype='uint16')
# Read files into the array
for i in range(0,len(MOLLIfiles)):
temp=dicom.read_file(MOLLIfiles[i]) # Read file
MOLLIims[:,:,i]=np.flipud(temp.pixel_array) # Read into the right part of the array
# save this file as an npy array for next time
if PreOrPost=='Pre':
np.save(os.path.join(os.path.split(self.datadirect)[0],'Analysis','MOLLIpre.npy'),MOLLIims)
#np.save(os.path.join(os.path.split(self.datadirect)[0],'Analysis','dyninfo.npy'),self.dyninfo)
self.MOLLIpre=MOLLIims
if PreOrPost=='Post':
np.save(os.path.join(os.path.split(self.datadirect)[0],'Analysis','MOLLIpost.npy'),MOLLIims)
#np.save(os.path.join(os.path.split(self.datadirect)[0],'Analysis','dyninfo.npy'),self.dyninfo)
self.MOLLIpost=MOLLIims
def checkDicomFile(filename):
"""
Проверяет, является ли выбранный файл корректным файлом DICOM
"""
error = False
try:
dicom.read_file(filename)
except:
error = True
return error
def testRead(self):
"""Unicode: Can read a file with unicode characters in name................"""
uni_name = u'test°'
try:
dicom.read_file(uni_name)
except UnicodeEncodeError:
self.fail("UnicodeEncodeError generated for unicode name")
# ignore file doesn't exist error
except IOError:
pass
def listdirRecursive(self, rootDir):
files = []
for root, subFolders, dirFiles in os.walk(rootDir):
for f in dirFiles:
try:
fileName = os.path.join(root,f)
dicom.read_file(fileName)
files.append(fileName)
except:
pass
return files
def load_dicom(filename):
try:
name = osp.splitext(osp.basename(filename))[0]
try:
data = dicomio.read_file(filename, force=True)
except TypeError:
data = dicomio.read_file(filename)
arr = data.pixel_array
return {name: arr}, None
except Exception as error:
return None, str(error)
def setUp(self):
dcm_path = path.join(test_dir,
'data',
'dcmstack',
'2D_16Echo_qT2',
'TE_20_SlcPos_-33.707626341697.dcm')
self.dcm = dicom.read_file(dcm_path)
self.stack = dcmstack.DicomStack()
self.stack.add_dcm(self.dcm)
self.dcm = dicom.read_file(dcm_path)
def get_LorR_from_bilateral(DicomDirectory, DynSeries_id, T2Series_id):
'''
This function takes a root directory with a bilateral scan and returns two subdirectories
nested inside abspath_PhaseID, one for LEFT breast and other for Right breast only
'''
# procees Dynamic
abspath_PhaseID = DicomDirectory+os.sep+DynSeries_id
# read and sort by location
[len_listSeries_files, sorted_FileNms_slices_stack] = ReadDicomfiles(abspath_PhaseID)
# simple separation between L and R
Left_slices = sorted_FileNms_slices_stack.iloc[:int(len_listSeries_files/2)]
Rigth_slices = sorted_FileNms_slices_stack.iloc[int(len_listSeries_files/2+1):]
os.chdir(abspath_PhaseID)
# preccess Left
os.mkdir(abspath_PhaseID+os.sep+'Left')
for i in range(len(Left_slices)):
dcmtomove = Left_slices.iloc[i,1]
proc = subprocess.Popen(['cp', dcmtomove, 'Left'+os.sep], stdout=subprocess.PIPE)
proc.wait()
# process Right
os.mkdir(abspath_PhaseID+os.sep+'Right')
for i in range(len(Rigth_slices)):
dcmtomove = Rigth_slices.iloc[i,1]
proc = subprocess.Popen(['cp', dcmtomove, 'Right'+os.sep], stdout=subprocess.PIPE)
proc.wait()
# extract left most slice position for each subvolume
# for left
[Leftlen_listSeries_files, Leftsorted_FileNms_slices_stack] = ReadDicomfiles(abspath_PhaseID+os.sep+'Left')
print Leftsorted_FileNms_slices_stack.values
Leftmostleft_slice = Leftsorted_FileNms_slices_stack.iloc[0]['slices']
dicomInfo_Left = dicom.read_file(abspath_PhaseID+os.sep+'Left'+os.sep+str(Leftmostleft_slice))
# Image Position (0020,0032): specifies the x, y, and z coordinates of the upper left hand corner of the image.
# his tag specifies the coordinates of the the first voxel transmitted.
Left_pos_pat = list(dicomInfo_Left[0x0020,0x0032].value)
# Image Orientation (0020,0037): specifies the direction cosines
Left_ori_pat = list(dicomInfo_Left[0x0020,0x0037].value)
print "Left DCE image_pos_pat: %s" % Left_pos_pat
# for Right
[Rightlen_listSeries_files, Rightsorted_FileNms_slices_stack] = ReadDicomfiles(abspath_PhaseID+os.sep+'Right')
print Rightsorted_FileNms_slices_stack.values
Rightmostleft_slice = Rightsorted_FileNms_slices_stack.iloc[0]['slices']
dicomInfo_Right = dicom.read_file(abspath_PhaseID+os.sep+'Right'+os.sep+str(Rightmostleft_slice))
# Image Position (0020,0032): specifies the x, y, and z coordinates of the upper left hand corner of the image.
# his tag specifies the coordinates of the the first voxel transmitted.
Right_pos_pat = list(dicomInfo_Right[0x0020,0x0032].value)
# Image Orientation (0020,0037): specifies the direction cosines
Right_ori_pat = list(dicomInfo_Right[0x0020,0x0037].value)
print "Right DCE image_pos_pat: %s" % Right_pos_pat
return Left_pos_pat, Left_ori_pat, Right_pos_pat, Right_ori_pat
def get_3Ddata(self, start=0, stop=None, step=1):
"""
Function make 3D data from dicom file slices
"""
data3d = []
dcmlist = self.dcmlist
# print 'stsp ', start, stop, step
if stop is None:
stop = len(dcmlist)
raw_max = None
raw_min = None
slope = None
inter = None
printRescaleWarning = False
for i in xrange(start, stop, step):
onefile = dcmlist[i]
data = dicom.read_file(onefile)
data2d = data.pixel_array
# mport pdb; pdb.set_trace()
if len(data3d) == 0:
shp2 = data2d.shape
data3d = np.zeros([len(dcmlist), shp2[0], shp2[1]],
dtype=np.int16)
mx = np.max(data2d)
mn = np.min(data2d)
if (raw_max is None) or (raw_max < mx):
raw_max = mx
if (raw_min is None) or (raw_min < mx):
raw_min = mn
try:
slope = data.RescaleSlope
inter = data.RescaleIntercept
if slope == 1 and inter == 0:
printRescaleWarning = True
slope = 0.5
inter = 0 # -16535
new_data2d = (np.float(slope) * data2d)\
+ np.float(inter)
except:
logger.warning(
'problem with RescaleSlope and RescaleIntercept')
print 'problem with RescaleSlope and RescaleIntercept'
traceback.print_exc()
print '----------'
new_data2d = (np.float(1) * data2d)\
+ np.float(0)
# first readed slide is at the end
data3d[-i - 1, :, :] = new_data2d
logger.debug("Data size: " + str(data3d.nbytes) + ', shape: ' +
str(shp2) + 'x' + str(len(dcmlist)) + ' file ' +
onefile)
if printRescaleWarning:
print "Automatic Rescale with slope 0.5"
logger.warning("Automatic Rescale with slope 0.5")
return data3d
def examinePhilips4DUS(self, filePath):
# currently only this one (bogus, non-standard) Philips 4D US format is supported
supportedSOPClassUID = '1.2.840.113543.6.6.1.3.10002'
# Quick check of SOP class UID without parsing the file...
try:
sopClassUID = slicer.dicomDatabase.fileValue(
filePath, self.tags['sopClassUID'])
if sopClassUID != supportedSOPClassUID:
# Unsupported class
return []
except Exception as e:
# Quick check could not be completed (probably Slicer DICOM database is not initialized).
# No problem, we'll try to parse the file and check the SOP class UID then.
pass
try:
ds = dicom.read_file(filePath, stop_before_pixels=True)
except Exception as e:
logging.debug("Failed to parse DICOM file: {0}".format(e.message))
return []
if ds.SOPClassUID != supportedSOPClassUID:
# Unsupported class
return []
confidence = 0.9
if ds.PhotometricInterpretation != 'MONOCHROME2':
logging.warning('Warning: unsupported PhotometricInterpretation')
confidence = .4
if ds.BitsAllocated != 8 or ds.BitsStored != 8 or ds.HighBit != 7:
logging.warning('Warning: Bad scalar type (not unsigned byte)')
confidence = .4
if ds.PhysicalUnitsXDirection != 3 or ds.PhysicalUnitsYDirection != 3:
logging.warning('Warning: Units not in centimeters')
confidence = .4
if ds.SamplesPerPixel != 1:
logging.warning('Warning: multiple samples per pixel')
confidence = .4
name = ''
if hasattr(ds, 'SeriesNumber') and ds.SeriesNumber:
name = '{0}:'.format(ds.SeriesNumber)
if hasattr(ds, 'Modality') and ds.Modality:
name = '{0} {1}'.format(name, ds.Modality)
if hasattr(ds, 'SeriesDescription') and ds.SeriesDescription:
name = '{0} {1}'.format(name, ds.SeriesDescription)
if hasattr(ds, 'InstanceNumber') and ds.InstanceNumber:
name = '{0} [{1}]'.format(name, ds.InstanceNumber)
loadable = DICOMLoadable()
loadable.files = [filePath]
loadable.name = name.strip(
) # remove leading and trailing spaces, if any
loadable.tooltip = "Philips 4D Ultrasound"
loadable.selected = True
loadable.confidence = confidence
return [loadable]
colors = tuple(np.array([con['color'] for con in contours]) / 255.0)
return label, colors
data_path = "C:/INFINITT/BNCT_TEMP"
patients = [
os.path.join(data_path, name) for name in os.listdir(data_path)
if os.path.isdir(os.path.join(data_path, name))
]
pat = patients[0]
for subdir, dirs, files in os.walk(pat):
dcms = glob.glob(os.path.join(subdir, "*.dcm"))
if len(dcms) == 1:
structure = dicom.read_file(os.path.join(subdir, files[0]))
contours = read_structure(structure)
elif len(dcms) > 1:
slices = [dicom.read_file(dcm) for dcm in dcms]
slices.sort(key=lambda x: float(x.ImagePositionPatient[2]))
image = np.stack([s.pixel_array for s in slices], axis=-1)
label, colors = get_mask(contours, slices)
plt.figure(figsize=(15, 15))
for i in range(9):
plt.subplot(3, 3, i + 1)
plt.imshow(image[..., i + 50], cmap="gray")
plt.contour(label[..., i + 50],
levels=[0.5, 1.5, 2.5, 3.5, 4.5],
colors=colors)
plt.axis('off')
def preprocess_image(filename, laterality):
dcm = dicom.read_file(filename)
m = center_crop_resize_filter(dcm.pixel_array, laterality)
return np.array([[m, m, m]])
def examineGeKretzUS(self, filePath):
# E Kretz uses 'Ultrasound Image Storage' SOP class UID
supportedSOPClassUID = '1.2.840.10008.5.1.4.1.1.6.1'
# Quick check of SOP class UID without parsing the file...
try:
sopClassUID = slicer.dicomDatabase.fileValue(
filePath, self.tags['sopClassUID'])
if sopClassUID != supportedSOPClassUID:
# Unsupported class
return []
except Exception as e:
# Quick check could not be completed (probably Slicer DICOM database is not initialized).
# No problem, we'll try to parse the file and check the SOP class UID then.
pass
try:
ds = dicom.read_file(
filePath,
defer_size=50) # use defer_size to not load large fields
except Exception as e:
logging.debug("Failed to parse DICOM file: {0}".format(e.message))
return []
if ds.SOPClassUID != supportedSOPClassUID:
# Unsupported class
return []
# Check if these expected DICOM tags are available:
# (7fe1,0011) LO [KRETZ_US] # 8, 1 PrivateCreator
# (7fe1,1101) OB 4b\52\45\54\5a\46\49\4c\45\20\31\2e\30\20\20\20\00\00\01\00\02\00... # 3471038, 1 Unknown Tag & Data
kretzUsTag = dicom.tag.Tag('0x7fe1', '0x11')
kretzUsDataTag = dicom.tag.Tag('0x7fe1', '0x1101')
if kretzUsTag not in ds.keys():
return []
if kretzUsDataTag not in ds.keys():
return []
confidence = 0.9
# These manufacturers values have been found in successfully loadable files:
# - Kretztechnik
# - GE Healthcare
# - GE Healthcare Austria GmbH & Co OG
if (ds.Manufacturer != 'Kretztechnik') and (
ds.Manufacturer.find('GE Healthcare') < 0):
logging.warning('Warning: unknown manufacturer: ' +
ds.Manufacturer)
confidence = .4
name = ''
if hasattr(ds, 'SeriesNumber') and ds.SeriesNumber:
name = '{0}:'.format(ds.SeriesNumber)
if hasattr(ds, 'Modality') and ds.Modality:
name = '{0} {1}'.format(name, ds.Modality)
if hasattr(ds, 'SeriesDescription') and ds.SeriesDescription:
name = '{0} {1}'.format(name, ds.SeriesDescription)
if hasattr(ds, 'InstanceNumber') and ds.InstanceNumber:
name = '{0} [{1}]'.format(name, ds.InstanceNumber)
name = name.strip() # remove leading and trailing spaces, if any
loadable = DICOMLoadable()
loadable.files = [filePath]
loadable.name = name
loadable.tooltip = "GE Kretz 3D Ultrasound"
loadable.warning = "Importing of this file format is experimental: images may be distorted, size measurements may be inaccurate."
loadable.selected = True
loadable.confidence = confidence
loadableHighRes1 = DICOMLoadable()
loadableHighRes1.files = loadable.files
loadableHighRes1.name = loadable.name + " (LR)"
loadableHighRes1.tooltip = loadable.tooltip + " (low-resolution)"
loadableHighRes1.warning = loadable.warning
loadableHighRes1.selected = False
loadableHighRes1.confidence = confidence
loadableHighRes2 = DICOMLoadable()
loadableHighRes2.files = loadable.files
loadableHighRes2.name = loadable.name + " (HR)"
loadableHighRes2.tooltip = loadable.tooltip + " (high-resolution)"
loadableHighRes2.warning = loadable.warning
loadableHighRes2.selected = False
loadableHighRes2.confidence = confidence
return [loadable, loadableHighRes1, loadableHighRes2]
import dicom
filepath = '/media/aether/My Passport/Medical Images Data/LCTSC - Lung CT Segmentation Challenge 2017/train/LCTSC-Train-S1-001/S1-001_countors/'
ds = dicom.read_file(filepath + "000000.dcm", force=True)
# print ds.dir("contour")
ctrs = ds.ROIContourSequence
# print len(ctrs) #5
# print len(ctrs[0]) #3
print ctrs[0].ContourSequence[0].ContourData
# ss = dicom.read_file('rtss.dcm')
# ss.ROIContours[0].Contours[0].ContourData
def vNavRead():
f, axarr = plt.subplots(1, 2)
#subjects = ["BANDA050","BANDA051","BANDA052","BANDA053","BANDA054","BANDA055","BANDA056","BANDA057","BANDA058","BANDA059","BANDA060"]
#subjects = ["BANDA004","BANDA005","BANDA006","BANDA007","BANDA008","BANDA009","BANDA010","BANDA011","BANDA012","BANDA013", "BANDA014", "BANDA015"]
#subjects = ["BANDA092","BANDA093","BANDA094","BANDA095","BANDA096","BANDA097","BANDA098","BANDA099", "BANDA100","BANDA101","BANDA102","BANDA103","BANDA104","BANDA105","BANDA106","BANDA107","BANDA108","BANDA109", "BANDA110","BANDA111","BANDA112","BANDA113","BANDA114","BANDA115","BANDA116","BANDA117","BANDA118","BANDA119"]
#,"BANDA088","BANDA089","BANDA090","BANDA091",]
#subjects = ["BANDA138","BANDA139","BANDA140"]
subjects = ["BANDA091"] #,"BANDA139","BANDA140"]
#["BANDA126","BANDA127","BANDA128","BANDA129","BANDA130","BANDA132","BANDA133","BANDA135","BANDA136","BANDA137","BANDA138","BANDA139","BANDA140"]
#["BANDA083","BANDA084","BANDA085","BANDA086","BANDA087"]
for s in subjects:
dicoms = glob.glob('/space/erebus/1/users/data/dicoms/' + s + '/MR*')
vnavsT1 = []
vnavsT2 = []
vnavsT1Score = []
vnavsT2Score = []
vnavsT1Comms = []
vnavsT2Comms = []
vNav = 0
vNav2 = 0
for d in dicoms:
dcm = dicom.read_file(d)
if dcm.ProtocolName == 'HCP_MGH_T1w_MPR_vNav' and dcm.SequenceName == 'ABCD3d1_32ns':
quat = dcm.ImageComments.split()
if vNav == 0 and len(vnavsT1Score) > 1:
vnavsT1Score = []
vnavsT1Comms.append(
str(dcm.AcquisitionNumber) + " " + dcm.ImageComments)
if int(dcm.AcquisitionNumber) > 1:
vnavsT1.append(
np.array([
float(quat[1]),
float(quat[2]),
float(quat[3]),
float(quat[4]),
float(quat[6]),
float(quat[7]),
float(quat[8])
]))
if len(vnavsT1) > 1:
vnavsT1Score.append(getvNavScore(vnavsT1))
print(vnavsT1Comms[len(vnavsT1Comms) - 2],
"vnav score:",
vnavsT1Score[len(vnavsT1Score) - 1])
vNav += 1
else:
vnavsT1.append(
np.array([0.0, 1.0, 0.0, 0.0, 0.0, 0.0, 0.0]))
vnavsT1Score.append(getvNavScore(vnavsT1))
print(vnavsT1Comms[len(vnavsT1Comms) - 2], "vnav score:",
vnavsT1Score[len(vnavsT1Score) - 1])
vNav = 0
elif dcm.ProtocolName == 'HCP_MGH_T2w_SPC_vNav' and dcm.SequenceName == 'ABCD3d1_32ns':
quat = dcm.ImageComments.split()
if vNav2 == 0 and len(vnavsT2Score) > 1:
vnavsT2Score = []
if int(dcm.AcquisitionNumber) > 1:
vnavsT2.append(
np.array([
float(quat[1]),
float(quat[2]),
float(quat[3]),
float(quat[4]),
float(quat[6]),
float(quat[7]),
float(quat[8])
]))
if len(vnavsT2) > 1:
vnavsT2Score.append(getvNavScore(vnavsT2))
vNav2 += 1
else:
vnavsT2.append(
np.array([0.0, 1.0, 0.0, 0.0, 0.0, 0.0, 0.0]))
vnavsT2Score.append(getvNavScore(vnavsT2))
vNav2 = 0
f = open(
"/space/erebus/1/users/data/preprocess/" + s +
"/motion/vnavsT1Score.csv", 'w')
f.write(str(vnavsT1Score).replace("[", "").replace("]", ""))
f.close()
f = open(
"/space/erebus/1/users/data/preprocess/" + s +
"/motion/vnavsT2Score.csv", 'w')
f.write(str(vnavsT2Score).replace("[", "").replace("]", ""))
f.close()
print(vnavsT1Score)
print(vnavsT2Score)
print(s, "T1", sum(np.array(vnavsT1Score) > 0.5))
print(s, "T2", sum(np.array(vnavsT2Score) > 0.5))
axarr[0].plot(range(len(vnavsT1Score)), vnavsT1Score, label=s)
axarr[0].set_xlabel('TR (T1)')
axarr[0].set_ylabel('vnav score')
axarr[1].plot(range(len(vnavsT2Score)), vnavsT2Score, label=s)
axarr[1].set_xlabel('TR (T2)')
axarr[1].set_ylabel('vnav score')
axarr[0].legend(ncol=3)
axarr[1].legend(ncol=3)
required=True)
parser.add_argument('-B', '--beamdir', help='Directory for BEAM model')
parser.add_argument('-D', '--dosxyzdir', help='Directory for dosxyznrc')
args = parser.parse_args()
if args.beamdir:
beamdir = args.beamdir
else:
beamdir = os.getenv('EGS_HOME') + '/BEAM_ARC'
if args.dosxyzdir:
dosxyzdir = args.dosxyzdir
else:
dosxyzdir = os.getenv('EGS_HOME') + '/dosxyznrc'
dcmplanfile = args.dcmplan
dcmplan = dicom.read_file(dcmplanfile)
patientname = dcmplan.PatientsName
patientid = dcmplan.PatientID
planname = dcmplan.RTPlanLabel
# open the serial of files for output
outpath = os.path.dirname(os.path.abspath(dcmplanfile)) + '/'
outpathbeam = outpath + 'beamnrc/'
outpathdose = outpath + 'dosxyznrc/'
if not os.path.exists(outpathbeam):
os.makedirs(outpathbeam)
if not os.path.exists(outpathdose):
os.makedirs(outpathdose)
filemainpart = patientid + '_' + planname
# Check for new file every 1ms
while not os.path.exists(nextFullFilename):
time.sleep(0.001)
# Maybe useful to have a timestamp
print(time.time())
# Give a little time for the file to be fully transferred
time.sleep(0.01)
if verbose:
print('File size is {0} bytes'.format(
os.path.getsize(nextFullFilename)))
# read in, convert to nifti, analyze, send file back
dicomObject = dicom.read_file(nextFullFilename)
niftiObject = dicomreaders.mosaic_to_nii(dicomObject)
dat = niftiObject.get_data()
print(dat.shape)
currentImage = currentImage + 1
if verbose:
print('Send')
linuxSocket.send(feedbackData)
except (KeyboardInterrupt):
print('Close')
linuxSocket.close()
def examineGeUSMovie(self, filePath):
supportedSOPClassUIDs = [
'1.2.840.10008.5.1.4.1.1.6.1' # UltrasoundImageStorage
]
# Quick check of SOP class UID without parsing the file...
try:
sopClassUID = slicer.dicomDatabase.fileValue(
filePath, self.tags['sopClassUID'])
if not sopClassUID in supportedSOPClassUIDs:
# Unsupported class
return []
except Exception as e:
# Quick check could not be completed (probably Slicer DICOM database is not initialized).
# No problem, we'll try to parse the file and check the SOP class UID then.
pass
try:
ds = dicom.read_file(
filePath,
defer_size=30) # use defer_size to not load large fields
except Exception as e:
logging.debug("Failed to parse DICOM file: {0}".format(e.message))
return []
if not ds.SOPClassUID in supportedSOPClassUIDs:
# Unsupported class
return []
geUsMovieGroupRootTag = dicom.tag.Tag('0x7fe1', '0x0010')
geUsMovieGroupRootItem = ds.get(geUsMovieGroupRootTag)
if not geUsMovieGroupRootItem:
return []
if geUsMovieGroupRootItem.name != 'Private Creator':
return []
if geUsMovieGroupRootItem.value != 'GEMS_Ultrasound_MovieGroup_001':
return []
confidence = 0.8
name = ''
if hasattr(ds, 'SeriesNumber') and ds.SeriesNumber:
name = '{0}:'.format(ds.SeriesNumber)
if hasattr(ds, 'Modality') and ds.Modality:
name = '{0} {1}'.format(name, ds.Modality)
if hasattr(ds, 'SeriesDescription') and ds.SeriesDescription:
name = '{0} {1}'.format(name, ds.SeriesDescription)
if hasattr(ds, 'InstanceNumber') and ds.InstanceNumber:
name = '{0} [{1}]'.format(name, ds.InstanceNumber)
loadable = DICOMLoadable()
loadable.files = [filePath]
loadable.name = name.strip(
) # remove leading and trailing spaces, if any
loadable.tooltip = "GE ultrasound image sequence"
loadable.warning = "Importing of this file format is experimental: images may be distorted, size measurements may be inaccurate."
loadable.selected = True
loadable.confidence = confidence
return [loadable]
def get_metaData(self, dcmlist=None, ifile=0):
"""
Get metadata.
Voxel size is obtained from PixelSpacing and difference of
SliceLocation of two neighboorhoding slices (first have index ifile).
Files in are used.
"""
if dcmlist is None:
dcmlist = self.dcmlist
if len(dcmlist) <= 0:
return {}
data = dicom.read_file(dcmlist[ifile])
try:
data2 = dicom.read_file(dcmlist[ifile + 1])
voxeldepth = float(np.abs(data.SliceLocation -
data2.SliceLocation))
except:
logger.warning('Problem with voxel depth. Using SliceThickness,' +
' SeriesNumber: ' + str(data.SeriesNumber))
try:
voxeldepth = float(data.SliceThickness)
except:
logger.warning('Probem with SliceThicknes, setting zero. ' +
traceback.format_exc())
voxeldepth = 0
try:
pixelsize_mm = data.PixelSpacing
except:
logger.warning('Problem with PixelSpacing. Using [1,1]')
pixelsize_mm = [1, 1]
voxelsize_mm = [
voxeldepth,
float(pixelsize_mm[0]),
float(pixelsize_mm[1]),
]
metadata = {
'voxelsize_mm': voxelsize_mm,
'Modality': data.Modality,
'SeriesNumber': self.series_number
}
try:
metadata['SeriesDescription'] = data.SeriesDescription
except:
logger.warning(
'Problem with tag SeriesDescription, SeriesNumber: ' +
str(data.SeriesNumber))
try:
metadata['ImageComments'] = data.ImageComments
except:
logger.warning('Problem with tag ImageComments, SeriesNumber: ' +
str(data.SeriesNumber))
try:
metadata['Modality'] = data.Modality
except:
logger.warning('Problem with tag Modality, SeriesNumber: ' +
str(data.SeriesNumber))
metadata['dcmfilelist'] = self.dcmlist
# mport pdb; pdb.set_trace()
return metadata
str(int(s.cell(row, 1).value))].append(valuelist)
# update LIDC annotation with series number, rather than scan id
import dicom
LIDCpath = '/media/data1/wentao/LIDC-IDRI/DOI/'
antdictscan = {}
for k, v in antdict.iteritems():
pid, scan = k.split('_')
hasscan = False
for sdu in os.listdir(os.path.join(LIDCpath, 'LIDC-IDRI-' + pid)):
for srs in os.listdir(
os.path.join(*[LIDCpath, 'LIDC-IDRI-' + pid, sdu])):
if srs.endswith('.npy'):
print('npy', pid, scan, srs)
continue
RefDs = dicom.read_file(
os.path.join(
*[LIDCpath, 'LIDC-IDRI-' + pid, sdu, srs, '000006.dcm']))
# print scan, str(RefDs[0x20, 0x11].value)
if str(RefDs[0x20, 0x11].value) == scan or scan == '0':
if hasscan: print('rep', pid, sdu, srs)
hasscan = True
antdictscan[pid + '_' + srs] = v
break
if not hasscan: print('not found', pid, scan, sdu, srs)
# find the match from LIDC-IDRI annotation
import math
lunaantdictnodid = {}
maxdist = 0
for srcid, lunaantlidc in lunantdictlidc.iteritems():
lunaantdictnodid[srcid] = []
pid, stdid = sidmap[srcid]
def load_data_1(
startpath='/home/tuixiangbeijingtest0/Desktop/workfolder/CR/',
big_batch=10000,
verbose=1,
nb_classes=2,
ycolindex=25, ## the column that we want to investigate
big_batch_index=0):
starttime = time.time()
rawtextcol = []
foldercol = []
foldercol1 = []
for ypath in ypathlist:
wb = xlrd.open_workbook(ypath)
sh = wb.sheet_by_index(0)
rawtextcol += sh.col_values(3)
foldercol += sh.col_values(5)
foldercol1 += sh.col_values(4)
#result0=sh.col_values(3)
#bodypartcol+=sh.col_values(3)
#ycol+=sh.col_values(ycolindex)
Xtest1 = []
Xtest2 = []
X_overall = []
Y_overall = []
chestposlist = []
rawtextlist = []
count = 0
count1 = 0
count11 = 0
selectcount = 0
selectratio = 1
#xls0=xlwt.Workbook(encoding='utf-8')
#xls1=xlwt.Workbook(encoding='utf-8')
#xls2=xlwt.Workbook(encoding='utf-8')
#sheet0=xls0.add_sheet('Sheet1')
#sheet1=xls1.add_sheet('Sheet1')
#sheet2=xls2.add_sheet('Sheet1')
#xls=xlwt.Workbook(encoding='utf-8')
#sheet1=xls.add_sheet('sheet1')
#for folderi in range(1,1000):
for folderi in range(1, sh.nrows):
#if count==450 and count1==225 and count11==225:
#break
folder = foldercol[folderi]
if len(folder) == 0:
pass
else:
#newpath=glob.glob(startpath+folder+'/Final*')
newpath = '/media/tuixiangbeijingtest0/f989fbc9-24a9-42ce-802e-902125737abd/srv/ruxian2' + foldercol1[
folderi] + foldercol[folderi] + 'hh'
#print(newpath)
if os.path.exists(newpath):
#bodypart=bodypartcol[folderi]
#print(newpath)
rawtext = rawtextcol[folderi]
tmp = dicom.read_file(
newpath
) #dicom.read_file("//home/tuixiangbeijingtest0/Desktop/Image_Decom/image1")
#bodypart=tmp.BodyPartExamined#bodypart=tmp['Body Part Examined'][0]
#rawtext=rawtext.replace('.','')
if hasattr(
tmp, 'BodyPartExamined'
) and tmp.BodyPartExamined == part and hasattr(
tmp, 'ViewPosition'
) and tmp.ViewPosition == position: #bodypart: #体位 X光
#ifbool=True
#for cont in controltextlist:
#if not cont in rawtext:
#ifbool=False
#break
#ifbool=True
#if str1 in rawtext:
if any(cont in rawtext for cont in indtext0) and (not all(
cont in rawtext
for cont in indtext1)) and (not all(
cont in rawtext
for cont in indtext2)) and count < 100:
#if (ifbool==True and not any(cont in rawtext for cont in indtext) and not any(cont in rawtext for cont in indtext2)): #or (any(wl in rawtext for wl in wllist) and all(zdy in rawtext for zdy in zdylist) and not any(cont in rawtext for cont in indtext) and not any(cont in rawtext for cont in indtext2)):
#if any(cont in rawtext for cont in controltextlist):
#tmp=sio.loadmat(newpath[0])
pos = tmp.ViewPosition #pos=tmp['View Position']
if pos == 'PA': #部位 X光
if selectcount % selectratio == 0:
#if count>=1000:
#continue
rawtextlist.append(rawtext)
#sheet0.write(count,0,rawtext)
#sheet0.write(count,1,'0')
#sheet2.write(count,0,rawtext)
#sheet2.write(count,1,'0')
chestposlist.append(pos)
imageData = cv2.resize(
tmp.pixel_array, (224, 224)
) #imageData=cv2.resize(x1.pixel_array,(224,224))
#imageData=misc.imresize(imageData,newsize)
#imageData=imageData[45:173,60:188]
#imageData=misc.imresize(imageData,newsize)
X_overall.append(imageData)
Y_overall.append(0)
Xtest1.append(imageData)
count += 1
#continue
'''
foldername='/home/tuixiangbeijingtest0/Desktop/workfolder/ttest/'+str(count)+'.png'
plt.clf()
plt.xlabel(0)
plt.imshow(imageData,cmap=plt.cm.Greys_r)
plt.savefig(foldername)
'''
elif any(cont in rawtext
for cont in indtext1) and (not all(
cont in rawtext
for cont in indtext0)) and count1 < 50:
#elif any(cont in rawtext for cont in indtext) and not(str2 in rawtext) and not(str3 in rawtext) and not(str4 in rawtext) and not(str5 in rawtext) and not(str6 in rawtext) and count1<550:
#tmp=sio.loadmat(newpath[0])
pos = tmp.ViewPosition #
if pos == 'PA':
selectcount += 1
#if count1>=1000:
#continue
rawtextlist.append(rawtext)
#sheet1.write(count1,1,rawtext)
#sheet1.write(count1,2,'1')
#sheet1.write(count1,3,'heart')
#sheet2.write(count1+1000,0,rawtext)
#sheet2.write(count1+1000,1,'1')
chestposlist.append(pos)
imageData = cv2.resize(
tmp.pixel_array, (224, 224)
) #imageData=cv2.resize(x1.pixel_array,(224,224))
#imageData=misc.imresize(imageData,newsize)
#imageData=imageData[45:173,60:188]
#imageData=misc.imresize(imageData,newsize)
X_overall.append(imageData)
Y_overall.append(1)
Xtest2.append(imageData)
count1 += 1
#continue
#print(count1)
#print(rawtext)
#sheet1.write(count1,1,rawtext)
#elif any(cont in rawtext for cont in indtext2):
#’‘’(any(wl in rawtext for wl in wllist) and not any(cont in rawtext for cont in controltextlist)) or‘’‘
#(any(wl in rawtext for wl in wllist) and
#elif ((any(wl in rawtext for wl in wllist) and any(cont in rawtext for cont in indtext2)) or any(cont in rawtext for cont in indtext2)) and not(str2 in rawtext) and count11<500:
#elif ((any(wl in rawtext for wl in wllist) and any(cont in rawtext for cont in indtext2)) or any(cont in rawtext for cont in indtext2)) and not(str2 in rawtext) and not(str3 in rawtext) and not(str4 in rawtext) and not(str5 in rawtext) and not(str6 in rawtext) and count11<450:
#elif any(cont in rawtext for cont in indtext2) and not(str2 in rawtext) and not(str3 in rawtext) and count11<500:
elif any(cont in rawtext
for cont in indtext2) and (not all(
cont in rawtext
for cont in indtext0)) and count11 < 50:
pos = tmp.ViewPosition #
if pos == 'PA':
selectcount += 1
rawtextlist.append(rawtext)
#sheet1.write(count11+500,1,rawtext)
#sheet1.write(count11+500,2,'1')
#sheet1.write(count11+500,3,'lung')
#sheet2.write(count11+1500,0,rawtext)
#sheet2.write(count11+1500,1,'1')
chestposlist.append(pos)
imageData = cv2.resize(
tmp.pixel_array, (224, 224)
) #imageData=cv2.resize(x1.pixel_array,(224,224))
#imageData=misc.imresize(imageData,newsize)
#imageData=imageData[45:173,60:188]
#imageData=misc.imresize(imageData,newsize)
X_overall.append(imageData)
Y_overall.append(1)
Xtest2.append(imageData)
count11 += 1
#continue
#print(count1)
#print(rawtext)
#sheet1.write(count1,1,rawtext.strip())
#xls.save('name1_1.xls')
'''
foldername='/home/tuixiangbeijingtest0/Desktop/workfolder/ttest/'+str(count)+'.png'
plt.clf()
plt.xlabel(1)
plt.imshow(imageData,cmap=plt.cm.Greys_r)
plt.savefig(foldername)
'''
#xls0.save('/home/tuixiangbeijingtest0/Desktop/ftp/heart&lung_0.xls')
#xls1.save('/home/tuixiangbeijingtest0/Desktop/ftp/heart&lung_1.xls')
#xls2.save('/home/tuixiangbeijingtest0/Desktop/ftp/heart&lung_1000.xls')
X_overall = np.array(X_overall) / 5000.0
Xshape = X_overall.shape
print(Xshape)
X_overall = X_overall.reshape(Xshape[0], Xshape[1] * Xshape[2])
Y_overall = np.array(Y_overall)
if verbose:
print("total time " + str(time.time() - starttime))
unique, counts = np.unique(Y_overall, return_counts=True)
print(np.mean(np.array(Xtest1)), np.mean(np.array(Xtest2)))
print(np.std(np.array(Xtest1)), np.std(np.array(Xtest2)))
print(counts, float(counts[0]) / float((counts[1] + counts[0])))
'''
#author: yangfan
#功能 根据混淆矩阵的索取得对应报告
#参数 indexlist 混淆矩阵对应的报告
#返回值 xlsbg.save 含有报告的xls
#使用方法 先得到混淆矩阵 然后取消此处的注视 然后运行模型代码 当控制台输出报告生成完毕 可停止模型
#注意事项 1.保存位置在/home/tuixiangbeijingtest0/Desktop/workfolder/xls/bgxls/下
#2.根据不同情况取不同的表名
#3.哪个模型的混淆矩阵下标list对应哪个模型 不能混淆 否则会出现匹配报告错误的情况 此处要细心
xlsbg=xlwt.Workbook(encoding='utf-8')
sheetbg=xlsbg.add_sheet('Sheet1')
X_validate_a=np.load('/home/tuixiangbeijingtest0/Desktop/workfolder/weights/vgg_transfer_lung/1462865076/X_validate.npy')
xlcount=0
indexlist=[66, 80, 124, 176, 190, 282, 301, 363, 382]
print('正在生成报告...')
for x_over in range(0,len(X_overall)):
for index in indexlist:
if(X_overall[x_over]==X_validate_a[index]).all():
#print(rawtextlist[xcount])
#for word in indtext2:
#if word in rawtextlist[x_over]:
#print('new')
#print('----------------------------------------------------')
#print(rawtextlist[x_over])
#print('111:',word)
#print('----------------------------------------------------')
#print('end')
#break
sheetbg.write(xlcount,1,rawtextlist[x_over])
xlcount+=1
#print(rawtextlist[x_over])
xlsbg.save('/home/tuixiangbeijingtest0/Desktop/workfolder/xls/bgxls/146286507456_15_01.xls')
print('报告生成完毕')
'''
return X_overall, Y_overall
def patchDicomDir(self, inputDirPath, outputDirPath):
"""
Since CTK (rightly) requires certain basic information [1] before it can import
data files that purport to be dicom, this code patches the files in a directory
with some needed fields.
Calling this function with a directory path will make a patched copy of each file.
Importing the old files to CTK should still fail, but the new ones should work.
The directory is assumed to have a set of instances that are all from the
same study of the same patient. Also that each instance (file) is an
independent (multiframe) series.
[1] https://github.com/commontk/CTK/blob/16aa09540dcb59c6eafde4d9a88dfee1f0948edc/Libs/DICOM/Core/ctkDICOMDatabase.cpp#L1283-L1287
"""
import dicom
self.addLog('DICOM patching started...')
logging.debug('DICOM patch input directory: ' + inputDirPath)
logging.debug('DICOM patch output directory: ' + outputDirPath)
for rule in self.patchingRules:
rule.logCallback = self.addLog
rule.processStart(inputDirPath, outputDirPath)
for root, subFolders, files in os.walk(inputDirPath):
currentSubDir = os.path.relpath(root, inputDirPath)
rootOutput = os.path.join(outputDirPath, currentSubDir)
# Notify rules that processing of a new subdirectory started
for rule in self.patchingRules:
rule.processDirectory(currentSubDir)
for file in files:
filePath = os.path.join(root, file)
self.addLog('Examining %s...' %
os.path.join(currentSubDir, file))
skipFileRequestingRule = None
for rule in self.patchingRules:
if rule.skipFile(currentSubDir):
skipFileRequestingRule = rule
break
if skipFileRequestingRule:
self.addLog(' Rule ' + rule.__class__.__name__ +
' requested to skip this file.')
continue
try:
ds = dicom.read_file(filePath)
except (IOError, dicom.filereader.InvalidDicomError):
self.addLog(' Not DICOM file. Skipped.')
continue
self.addLog(' Patching...')
for rule in self.patchingRules:
rule.processDataSet(ds)
patchedFilePath = os.path.abspath(
os.path.join(rootOutput, file))
for rule in self.patchingRules:
patchedFilePath = rule.generateOutputFilePath(
ds, patchedFilePath)
######################################################
# Write
dirName = os.path.dirname(patchedFilePath)
if not os.path.exists(dirName):
os.makedirs(dirName)
self.addLog(' Writing DICOM...')
dicom.write_file(patchedFilePath, ds)
self.addLog(' Created DICOM file: %s' % patchedFilePath)
self.addLog(
'DICOM patching completed. Patched files are written to:\n{0}'.
format(outputDirPath))
def build_xls(xlsx_file,
dicom_paths,
sem_xlsx_file,
wrongs=[None, None],
rights=[None, None]):
sem_file = openpyxl.load_workbook(sem_xlsx_file)
sem_sheet = sem_file.active
if os.path.exists(xlsx_file):
os.remove(xlsx_file)
wb = openpyxl.Workbook()
ws = wb.active
for i in range(len(dicom_paths)):
data = dicom.read_file(dicom_paths[i])
r = i + 1
c = 0
#Patient ID
c += 1
patient = data[0x10, 0x10][:]
if r == 1:
ws.cell(row=r, column=c, value='Patient_ID')
else:
ws.cell(row=r, column=c, value=patient)
#Patient always or mostly wrong or right?
if len(wrongs) == len(rights):
if len(wrongs) == 2:
c += 1
if r == 1:
if wrongs[1] in ['Always', 'always']:
ws.cell(row=r, column=c, value='Always...')
elif wrongs[1] in ['Mostly', 'mostly']:
ws.cell(row=r, column=c, value='Mostly...')
elif wrongs[1] not in [
'Always', 'always', 'Mostly', 'mostly'
]:
raise IOError(
'wrongs[1] and rights[1] must both be "Always" or "Mostly"'
)
else:
if patient in wrongs[0]:
ws.cell(row=r, column=c, value='wrong')
elif patient in rights[0]:
ws.cell(row=r, column=c, value='right')
else:
raise IOError(
'wrongs and rights take exactly 2 arguments, {} given'.
format(len(wrongs)))
else:
raise IOError(
'wrongs and rights must be same length, and both "Always" or both "Mostly"'
)
#Patient sex
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Sex')
else:
ws.cell(row=r, column=c, value=data[0x10, 0x40].value)
#Patient age
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Age')
else:
for i in range(1, sem_sheet.max_column):
if sem_sheet.cell(row=1, column=i).value == 'Age':
column_index = i
break
for i in range(1, sem_sheet.max_row):
if sem_sheet.cell(row=i, column=1).value == patient:
ws.cell(row=r,
column=c,
value=sem_sheet.cell(row=i,
column=column_index).value)
break
#Location
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Tumour location')
else:
for i in range(1, sem_sheet.max_column):
if sem_sheet.cell(row=1, column=i).value == 'Localisation':
column_index = i
break
for i in range(1, sem_sheet.max_row):
if sem_sheet.cell(row=i, column=1).value == patient:
ws.cell(row=r,
column=c,
value=sem_sheet.cell(row=i,
column=column_index).value)
break
#Depth
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Tumour depth')
else:
for i in range(1, sem_sheet.max_column):
if sem_sheet.cell(row=1, column=i).value == 'Depth_Melissa':
column_index = i
break
for i in range(1, sem_sheet.max_row):
if sem_sheet.cell(row=i, column=1).value == patient:
ws.cell(row=r,
column=c,
value=sem_sheet.cell(row=i,
column=column_index).value)
break
#Manufacturer
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Manufacturer')
else:
ws.cell(row=r, column=c, value=data[0x08, 0x70].value)
#Scanner model
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Model')
else:
ws.cell(row=r, column=c, value=data[0x08, 0x1090].value)
#Institution name
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Institution')
else:
try:
ws.cell(row=r, column=c, value=data[0x08, 0x80].value)
except KeyError:
ws.cell(row=r, column=c, value='-')
#Station name
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Station')
else:
try:
ws.cell(row=r, column=c, value=data[0x08, 0x1010].value)
except KeyError:
ws.cell(row=r, column=c, value='-')
#Slice thickness
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Slice thickness')
else:
ws.cell(row=r, column=c, value=data[0x18, 0x50].value)
#Repetition time
c += 1
if r == 1:
ws.cell(row=r, column=c, value='RT')
else:
ws.cell(row=r, column=c, value=data[0x18, 0x80].value)
#Echo time
c += 1
if r == 1:
ws.cell(row=r, column=c, value='ET')
else:
ws.cell(row=r, column=c, value=data[0x18, 0x81].value)
#Magnetic field strength
c += 1
if r == 1:
ws.cell(row=r, column=c, value='B0')
else:
ws.cell(row=r, column=c, value=data[0x18, 0x87].value)
#Spacing between slices
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Slice spacing')
else:
ws.cell(row=r, column=c, value=data[0x18, 0x88].value)
#Smalles image pixel value
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Smallest pixel value')
#else:
#ws.cell(row=r, column=c, value=data[0x28, 0x0106].value)
#Largest image pixel value
c += 1
if r == 1:
ws.cell(row=r, column=c, value='Largest pixel value')
#else:
#ws.cell(row=r, column=c, value=data[0x28, 0x0107].value)
wb.save(xlsx_file)
print('file written to {}'.format(xlsx_file))
return
def __init__(self, folder1, file1):
self.folder1 = folder1
self.file1 = file1
Imxray1 = dicom.read_file(self.folder1 + self.file1 + ".dcm")
Image.__init__(self, Imxray1.pixel_array)
import os
import glob as gb
import numpy as np
import cv2
import matplotlib.pyplot as plt
import dicom
# 提取轮廓的窗宽 窗位
WL,WW=-360,446
dcm_dir='image.dcm'
dcm = dicom.read_file(dcm_dir)
img_origin = dcm.pixel_array * dcm.RescaleSlope + dcm.RescaleIntercept
img_abdoment = (img_origin - (WL - WW / 2)) / WW * 255 # (x-min)/(max-min)
img_abdoment[img_abdoment < 0] = 0
img_abdoment[img_abdoment > 255] = 255
plt.subplot(1,4,1)
plt.title('ww_wl')
plt.imshow(img_abdoment, cmap='Greys_r')
#===========================================
dicom_np = np.uint8(img_abdoment)
ret, img = cv2.threshold(dicom_np,90,255, cv2.THRESH_BINARY) # 二值化
im2, contours, _ = cv2.findContours(img, cv2.RETR_LIST, cv2.CHAIN_APPROX_SIMPLE) # 查找轮廓
# cv2.drawContours(dicom_np, contours, -1, (0, 255, 255), 2) # 填充轮廓颜色
plt.subplot(1, 4, 2)
plt.title('contours')
plt.imshow(dicom_np, cmap='gray')
from .. import dicomwrappers as didw
from .. import dicomreaders as didr
from ...volumeutils import endian_codes
from unittest import TestCase
from nose.tools import (assert_true, assert_false, assert_equal,
assert_not_equal, assert_raises)
from numpy.testing import assert_array_equal, assert_array_almost_equal
IO_DATA_PATH = pjoin(dirname(__file__), 'data')
DATA_FILE = pjoin(IO_DATA_PATH, 'siemens_dwi_1000.dcm.gz')
DATA_FILE_PHILIPS = pjoin(IO_DATA_PATH, 'philips_mprage.dcm.gz')
if have_dicom:
DATA = dicom.read_file(gzip.open(DATA_FILE))
DATA_PHILIPS = dicom.read_file(gzip.open(DATA_FILE_PHILIPS))
else:
DATA = None
DATA_PHILIPS = None
DATA_FILE_B0 = pjoin(IO_DATA_PATH, 'siemens_dwi_0.dcm.gz')
DATA_FILE_SLC_NORM = pjoin(IO_DATA_PATH, 'csa_slice_norm.dcm')
DATA_FILE_DEC_RSCL = pjoin(IO_DATA_PATH, 'decimal_rescale.dcm')
DATA_FILE_4D = pjoin(IO_DATA_PATH, '4d_multiframe_test.dcm')
# This affine from our converted image was shown to match our image spatially
# with an image from SPM DICOM conversion. We checked the matching with SPM
# check reg. We have flipped the first and second rows to allow for rows, cols
# transpose in current return compared to original case.
EXPECTED_AFFINE = np.array( # do this for philips?
[[-1.796875, 0, 0, 115],
def read_dicom_ed(PathDicom, contour_type='icontour'):
# path to dicom files
p2dcom = PathDicom + '/P' + patientID + 'dicom'
# delete tif folder if exist
path2tif = PathDicom + '/tifED'
if os.path.exists(path2tif):
shutil.rmtree(path2tif)
print 'tif folder was deleted.'
# create new tif folder
os.mkdir(path2tif)
# get the list and and path to dicom files
lstFilesDCM = [] # create an empty list
for dirName, subdirList, fileList in os.walk(p2dcom):
for filename in fileList:
if ".dcm" in filename.lower(): # check whether the file's DICOM
lstFilesDCM.append(os.path.join(dirName, filename))
# Get ref file
RefDs = dicom.read_file(lstFilesDCM[0])
# load total number of phases
nphases = RefDs.CardiacNumberofImages
# read text file which contains the list of manual contours
path2txt = glob.glob(PathDicom + '/*.txt')
txt = open(path2txt[0])
manuallst = txt.readlines()
# Load dimensions based on the number of rows, columns, and slices (along the Z axis)
ConstPixelDims = (int(RefDs.Rows), int(RefDs.Columns), len(manuallst) / 2)
# loop through all the DICOM files
k = 0
for manualfilename in manuallst:
# only dicom file with contour_type is loaded
filenameDCM = dirName + '/' + manualfilename[31:-22] + '.dcm'
if manualfilename[40:48] == contour_type: # only internal contours
if int(manualfilename[36:39]) % nphases == 0:
print 'dicom file: ', filenameDCM
ds = dicom.read_file(filenameDCM)
# read manual polygon
manfn = dirName[:-8] + manualfilename[
12:-31] + '/' + manualfilename[31:-2]
polygonxy = np.loadtxt(manfn)
# store the raw image data
if k == 0:
ArrayDicom = np.expand_dims(ds.pixel_array, axis=2)
tmp1 = poly2mask(polygonxy[:, 1], polygonxy[:, 0],
ConstPixelDims[0:2])
ArrayMask = np.expand_dims(tmp1, axis=2)
else:
ArrayDicom = np.append(ArrayDicom,
np.expand_dims(ds.pixel_array,
axis=2),
axis=2)
tmp1 = poly2mask(polygonxy[:, 1], polygonxy[:, 0],
ConstPixelDims[0:2])
ArrayMask = np.append(ArrayMask,
np.expand_dims(tmp1, axis=2),
axis=2)
plt.imsave(path2tif + '/' + manualfilename[31:-22] + '.tif',
ArrayDicom[:, :, k],
cmap=plt.cm.gray)
plt.imsave(path2tif + '/' + manualfilename[31:-22] +
'_mask.tif',
ArrayMask[:, :, k],
cmap=plt.cm.gray)
k = k + 1
return ArrayDicom, ArrayMask
import dicom # for reading dicom files
import os # for doing directory operations
import pandas as pd # for some simple data analysis (right now, just to load in the labels data and quickly reference it)
import numpy as np
labels = pd.read_csv('mass-data.csv', usecols=[0,2,3,4,8])
labels['path'] = ("")
for index, row in labels.iterrows():
labels.iloc[index, labels.columns.get_loc('path')] = 'Mass-Training_'+str(row['patient_id'])+'_'+row['side']+'_'+row['view']+'_'+str(row['abn_num'])
# row['path'] = 'Mass-Training_'+row['patient_id']+'_'+row['side']+'_'+row['view']+'_'+row['abn_num']
labels.pop('side')
labels.pop('view')
labels.pop('abn_num')
labels.pop('patient_id')
dir = os.walk("DOI")
for index, row in labels.iterrows():
if(os.path.isdir("DOI/"+row["path"])):
folder = os.listdir("DOI/"+row["path"])
folder = [x for x in folder if x != ".DS_Store"]
if(os.path.isdir("DOI/"+row["path"]+"/"+folder[0])):
folder2 = os.listdir("DOI/"+row["path"]+"/"+folder[0])
folder2 = [x for x in folder2 if x != ".DS_Store"]
ds=dicom.read_file("DOI/"+row["path"]+"/"+folder[0]+"/"+folder2[0]+"/"+"000000.dcm")
print(ds)
def readSIEMENSFlow(args):
print( colored.green("\nLooking for flow data... \n"))
MagPathStr = args.input
foldersList = [os.path.join(MagPathStr,o) for o in os.listdir(MagPathStr) if os.path.isdir(os.path.join(MagPathStr,o))]
if not foldersList:
filesListTEMP = glob.glob(MagPathStr + "/*")
ds = dicom.read_file(filesListTEMP[0])
if "SIEMENS" in ds.Manufacturer:
print("It's SIEMENS sequence!")
else:
print("We currently can not load files from " + ds.Manufacturer + ".")
else:
for dirName in foldersList:
filesListTEMP = glob.glob(dirName + "/*")
ds = dicom.read_file(filesListTEMP[0])
if "SIEMENS" in ds.Manufacturer:
proceed = True
if "magnitude" in ds.ImageComments:
PathFlowDataMAG = dirName
print(colored.cyan("Mag folder is: " + PathFlowDataMAG))
if "phase" in ds.ImageComments:
PathFlowData = dirName
print(colored.cyan("Flow folder is: " + PathFlowData))
#ConstDimsTemp = (int(ds.Rows), int(ds.Columns), len(filesListTEMP))
#dXY = ds.PixelSpacing
#dZ = ds.SpacingBetweenSlices
#pixel_spc = (dXY[0],dXY[1],dZ)
#print(pixel_spc)
else:
proceed = False
print(colored.red("FatalError: We currently can not load files from " + ds.Manufacturer + "."))
sys.exit()
# MagPathStr = str(FolderPath)
# PathList=MagPathStr.split("/")
# basePath = MagPathStr.replace(PathList[-1],"")
if proceed:
flowData = None
for folderNumber in range(0,2):
# sliceLocation = []
# flow files list
lstFilesDCM = []
# triggerTime = []
if folderNumber == 0:
folderPath = PathFlowDataMAG
print(colored.cyan("Reading the Magnitude files."))
if folderNumber == 1:
if args.segmentation:
break
folderPath = PathFlowData
print(colored.cyan("Reading the flow files ."))
################## Reading time of flight files
# listing magnitude files
for dirName, subdirList, fileList in os.walk( folderPath + "/"):
for filename in fileList:
# if ".dcm" in filename.lower(): # check whether the file's DICOM
lstFilesDCM.append(os.path.join(dirName,filename))
# ds = dicom.read_file(lstFilesDCM[-1])
# sliceLocation.append(ds.SliceLocation)
# triggerTime.append(ds.TriggerTime)
# Get ref file
RefDs = dicom.read_file(lstFilesDCM[0])
# triggerTimeTemp = sorted(set(triggerTime), key=float)
#print(triggerTimeTemp)
#sliceLocationTemp = set(sliceLocation)
# sliceLocationTemp = sorted(set(sliceLocation), key=float)
#print(sliceLocationTemp)
if folderNumber == 0:
ConstPixelDims = (int(RefDs.Rows), int(RefDs.Columns), len(lstFilesDCM))
dXY = ds.PixelSpacing
dZ = ds.SliceThickness
pixel_spc = (dXY[0],dXY[1],dZ)
MagData = numpy.zeros(ConstPixelDims, dtype=numpy.double)
for iFile in lstFilesDCM:
dsTemp = dicom.read_file (iFile)
MagData[:,:,int(dsTemp.InstanceNumber)-1]= dsTemp.pixel_array.astype('float')
#print(MagData.shape)
# print(RefDs)
MagDataAve = numpy.reshape(MagData, (int(RefDs.Rows), int(RefDs.Columns),len(lstFilesDCM)/int(RefDs.CardiacNumberofImages), RefDs.CardiacNumberofImages), order='F')
#print(MagDataAve.shape)
magDataTemp = MagDataAve.mean(3)
# magDataRevX = numpy.flip(magDataTemp, 0)
# magDataRevZ = numpy.flip(magDataRevX, 2)
magSize = magDataTemp.shape
totalNodes = magSize[0] * magSize[1] * magSize[2]
if args.vtk:
saveVTKSeg(magDataTemp,False,False, pixel_spc, totalNodes, args.output)
if args.mat:
scipy.io.savemat(args.output + "/mag.mat", mdict={'magDataTemp': magDataTemp})
# numpy.save(args.output +"/mag", magDataTemp)
else :
if flowData is None:
ConstFlowPixelDims = (int(RefDs.Rows), int(RefDs.Columns),len(lstFilesDCM))
flowDataTemp = numpy.zeros(ConstFlowPixelDims, dtype=numpy.double)
sliceLocationTemp = numpy.zeros([len(lstFilesDCM),2], dtype=numpy.double)
# icounter = 0
for iFile in lstFilesDCM:
dsTemp = dicom.read_file (iFile)
flowDataTemp[:,:,int(dsTemp.InstanceNumber)-1]= dsTemp.pixel_array.astype('int')
sliceLocationTemp[int(dsTemp.InstanceNumber)-1] = numpy.array([int(dsTemp.InstanceNumber)-1, float(dsTemp.SliceLocation)])
# icounter += 1
print(sliceLocationTemp.shape)
print(sliceLocationTemp)
sys.exit()
#print(flowDataTemp.shape)
flowDataTemp = numpy.reshape(flowDataTemp, (int(RefDs.Rows), int(RefDs.Columns),len(lstFilesDCM)/3, 3), order='F')
UAll = flowDataTemp[:,:,:,args.velocityorder[0]].squeeze()
VAll = flowDataTemp[:,:,:,args.velocityorder[1]].squeeze()
WAll = flowDataTemp[:,:,:,args.velocityorder[2]].squeeze()
UOrg = numpy.zeros([int(RefDs.Rows), int(RefDs.Columns),len(lstFilesDCM)/30,10], dtype=numpy.double)
VOrg = numpy.zeros([int(RefDs.Rows), int(RefDs.Columns),len(lstFilesDCM)/30,10], dtype=numpy.double)
WOrg = numpy.zeros([int(RefDs.Rows), int(RefDs.Columns),len(lstFilesDCM)/30,10], dtype=numpy.double)
UOrg[:,:,:,0] = UAll[:,:,0:30]
UOrg[:,:,:,1] = UAll[:,:,30:60]
VOrg[:,:,:,0] = VAll[:,:,0:30]
VOrg[:,:,:,1] = VAll[:,:,30:60]
WOrg[:,:,:,0] = WAll[:,:,0:30]
WOrg[:,:,:,1] = WAll[:,:,30:60]
# flowDataTemp = numpy.reshape(flowDataTemp, (int(RefDs.Rows), int(RefDs.Columns),len(lstFilesDCM)/3/int(RefDs.CardiacNumberofImages), 3, int(RefDs.CardiacNumberofImages)), order='F')
#sliceLocationTemp = numpy.reshape(sliceLocationTemp, (len(lstFilesDCM)/3,2, 3), order='F')
#flowDataRevX = numpy.flip(flowDataTemp, 0)
#flowDataRevZ = numpy.flip(flowDataRevX, 2)
# sliceLocations = numpy.unique(sliceLocationTemp[:,1])
# print(len(sliceLocations))
# sliceLocationsIndeces = (numpy.array(numpy.where(sliceLocationTemp[:,1] == sliceLocations[0])))
# print(numpy.array(numpy.where(sliceLocationTemp[:,1] == sliceLocations[0])).shape)
# sys.exit()
# for jj in range(0,len(sliceLocations)-1):
# #for ii in range(0,int(RefDs.CardiacNumberofImages)-1):
# if sliceLocationsIndeces[1,jj] < 300:
# UOrg[:,:,jj,ii] = flowDataTemp[:,:,jj,0].squeeze()
#
#USlice = numpy.sort(sliceLocationTemp[0:300], axis=1)
# print(USlice)
#UOrg = flowDataTemp[:,:,ii,0].squeeze()
#USliceLocation = sliceLocationTemp[ii,:]
#USliceLocationSort = numpy.sort(USliceLocation, axis=1)
# sliceUnique = numpy.unique(sliceLocationTemp[0:300,:], axis = 0)
# print(sliceUnique)
#
# elif 299 < ii < 600:
# VOrg = flowDataTemp[:,:,ii,1].squeeze()
# VOrgSliceLocation = sliceLocationTemp[ii,:]
# elif 599 < ii < 900:
# WOrg = flowDataTemp[:,:,ii,2].squeeze()
# WOrgSliceLocation = sliceLocationTemp[ii,:]
# selector = 0
# if args.segmentation is False:
# ### The combination of x +y and -z and permuted x and y is working. Ali Aug24 2017
# UOrg = args.velocitysign[0] * (flowDataTemp[:, :, :, args.velocityorder[0]].squeeze())
# VOrg = args.velocitysign[1] * (flowDataTemp[:, :, :, args.velocityorder[1]].squeeze())
# WOrg = args.velocitysign[2] * (flowDataTemp[:, :, :, args.velocityorder[2]].squeeze())
#
flowCorrected = numpy.zeros([flowDataTemp.shape[0], flowDataTemp.shape[1], flowDataTemp.shape[2]/10,3,10])
# #if args.eddycurrent:
# # flowCorrected = eddyCurrentCorrection(UOrg, VOrg, WOrg, args.randomnoise, args.eddythreshold, args.eddyplane)
#elif args.randomnoise is not None:
# flowCorrected = randNoise(args, UOrg, VOrg, WOrg, args.randomnoise/100, 0, 1)
#else:
flowCorrected[:, :, :,0, :] = UOrg
flowCorrected[:, :, :,1, :] = VOrg
flowCorrected[:, :, :,2, :] = WOrg
if args.mat:
scipy.io.savemat(args.output + "/vel.mat", mdict={'flowData': flowData})
#print(flowData.shape)
if args.vtk:
# if args.segmentation:
# saveVTKSeg(magDataTemp,False,False, pixel_spc, totalNodes, args.output)
# else:
saveVTK(magDataTemp, flowCorrected,pixel_spc, totalNodes, args.output)
# if args.eddycurrent:
# flowCorrected = eddyCurrentCorrection(UOrg, VOrg, WOrg, args.randomnoise, args.eddythreshold, args.eddyplane)
# elif args.randomnoise is not None:
# flowCorrected = randNoise(args, UOrg, VOrg, WOrg, args.randomnoise/100, 0, 1)
# else:
# flowCorrected[:, :, :,0, :] = UOrg
# flowCorrected[:, :, :,1, :] = VOrg
# flowCorrected[:, :, :,2, :] = WOrg
print(colored.green("\nGetting ready to write files... This takes a little bit of time"))
# magSize = magDataTemp.shape
#totalNodes = magSize[0] * magSize[1] * magSize[2]
#if (args.vtk == False and args.mat == False):
# print(colored.yellow("We will ONLY save in npy format, since you didnt select your preference! (VTK or MAT)"))
#if not args.segmentation:
# numpy.save(args.output +"/FlowData", flowCorrected)
#if args.vtk:
# if args.segmentation:
# saveVTKSeg(magDataTemp,False,False, pixel_spc, totalNodes, args.output)
# else:
# saveVTK(magDataTemp, flowCorrected,pixel_spc, totalNodes, args.output)
#if args.mat:
# if args.segmentation:
# with open(args.output + "/FlowData.mat", 'wb') as matlabFile:
# scipy.io.savemat(matlabFile, mdict={'magnitude': magDataTemp})
# else:
# with open(args.output + "/FlowData.mat", 'wb') as matlabFile:
# scipy.io.savemat(matlabFile, mdict={'velocity': flowData})
# scipy.io.savemat(matlabFile, mdict={'magnitude': magDataTemp})
return RefDs
def loadPhilips4DUSAsMultiVolume(self, loadable):
"""Load the selection as an Ultrasound, store in MultiVolume
"""
# get the key info from the "fake" dicom file
filePath = loadable.files[0]
ds = dicom.read_file(filePath, stop_before_pixels=True)
columns = ds.Columns
rows = ds.Rows
slices = ds[(0x3001, 0x1001)].value # private tag!
spacing = (
ds.PhysicalDeltaX * 10,
ds.PhysicalDeltaY * 10,
ds[(0x3001, 0x1003)].value * 10 # private tag!
)
frames = int(ds.NumberOfFrames)
imageComponents = frames
# create the correct size and shape vtkImageData
image = vtk.vtkImageData()
imageShape = (slices, rows, columns, frames)
image.SetDimensions(columns, rows, slices)
image.AllocateScalars(vtk.VTK_UNSIGNED_CHAR, imageComponents)
from vtk.util.numpy_support import vtk_to_numpy
imageArray = vtk_to_numpy(
image.GetPointData().GetScalars()).reshape(imageShape)
# put the data in a numpy array
# -- we need to read the file as raw bytes
pixelShape = (frames, slices, rows, columns)
pixels = numpy.fromfile(filePath, dtype=numpy.uint8)
pixelSize = reduce(lambda x, y: x * y, pixelShape)
headerSize = len(pixels) - pixelSize
pixels = pixels[headerSize:]
pixels = pixels.reshape(pixelShape)
slicer.modules.imageArray = imageArray
slicer.modules.pixels = pixels
# copy the data from numpy to vtk (need to shuffle frames to components)
for frame in range(frames):
imageArray[:, :, :, frame] = pixels[frame]
# create the multivolume node and display it
multiVolumeNode = slicer.vtkMRMLMultiVolumeNode()
multiVolumeNode.SetScene(slicer.mrmlScene)
multiVolumeDisplayNode = slicer.mrmlScene.CreateNodeByClass(
'vtkMRMLMultiVolumeDisplayNode')
multiVolumeDisplayNode.SetReferenceCount(
multiVolumeDisplayNode.GetReferenceCount() - 1)
multiVolumeDisplayNode.SetScene(slicer.mrmlScene)
multiVolumeDisplayNode.SetDefaultColorMap()
slicer.mrmlScene.AddNode(multiVolumeDisplayNode)
multiVolumeNode.SetAndObserveDisplayNodeID(
multiVolumeDisplayNode.GetID())
multiVolumeNode.SetAndObserveImageData(image)
multiVolumeNode.SetNumberOfFrames(frames)
multiVolumeNode.SetName(loadable.name)
slicer.mrmlScene.AddNode(multiVolumeNode)
#
# automatically select the volume to display
#
appLogic = slicer.app.applicationLogic()
selNode = appLogic.GetSelectionNode()
selNode.SetReferenceActiveVolumeID(multiVolumeNode.GetID())
appLogic.PropagateVolumeSelection()
return multiVolumeNode
def dicom_to_array(filename):
d = dicom.read_file(filename)
a = d.pixel_array
return np.array(a)
def make_svs_anatomical(population, workspace, voxel_name):
for subject in population:
subject_dir = os.path.join(workspace, subject)
dicom_dir = os.path.join(subject_dir, 'DICOM')
svs_dir = os.path.join(subject_dir, 'SVS')
nifti_dir = mkdir_path(os.path.join(subject_dir, 'NIFTI'))
########## Get MP2RAGE UNI
if not os.path.isfile( os.path.join(nifti_dir, 'ANATOMICAL.nii')):
print 'Converting MP2RAGE '
dicoms = [os.path.join(dicom_dir, dicom) for dicom in os.listdir(dicom_dir)]
T1_list = []
for dicom in dicoms:
try:
dcm_read = pydicom.read_file(dicom, force=True)
sequence = dcm_read.SeriesDescription
except AttributeError:
continue
if 'mp2rage_p3_602B_UNI_Images' in sequence:
T1_list.append(dicom)
# convert T1 anatomical to NIFTI with SPM
print 'Converting Dicom to Nifti for %s' % subject
spm_dicom_convert = spmu.DicomImport()
spm_dicom_convert.inputs.format = 'nii'
spm_dicom_convert.inputs.in_files = T1_list
spm_dicom_convert.inputs.output_dir = nifti_dir
spm_dicom_convert.run()
# rename output file
os.system('mv %s/*nii %s/ANATOMICAL.nii' %(nifti_dir, nifti_dir))
# make svs mask
rda =[]
if not os.path.isfile(os.path.join(svs_dir, voxel_name, 'RDA', '.nii')):
for root, dirs, files, in os.walk(os.path.join(svs_dir, voxel_name, 'RDA'), topdown=False):
for name in files:
if 'supp' in name and 'edit1' in name:
rda.append(os.path.join(name))
if rda is []:
print 'RDA metabolite data does not exist for subject %s' % subject
T1Path = os.path.join(subject_dir, 'NIFTI' + '/')
T1Image = 'ANATOMICAL.nii'
svs_path = os.path.join(svs_dir, voxel_name, 'RDA' + '/')
svs_file = rda[0]
matlab_command = ['matlab', '--version', '8.2', '-nodesktop', '-nosplash', '-nojvm',
'-r "RDA_TO_NIFTI(\'%s\', \'%s\', \'%s\', \'%s\') ; quit;"'
% (T1Path, T1Image, svs_path, svs_file)]
subprocess.call(matlab_command)
os.system('mv %s/*Mask.nii %s' % (nifti_dir, os.path.join(svs_dir, voxel_name, 'RDA')))
os.system('mv %s/*coord.txt %s' % (nifti_dir, os.path.join(svs_dir, voxel_name, 'RDA')))
method = "1-localizer"
method = "3-ep2d_diff_M128_b0_1000_DIN_ADC"
method = "6-t2_spc_ns_sag_p2_iso"
method = "7-spctra"
method = "4-t2_tse_tra_512_5mm"
method = "2-ep2d_diff_M128_b0_1000_DIN"
method = "5-t1_fl2d_tra"
baseName = base + "/" + patient + "/" + patient + "-" + date + "/" + method
if __name__ == "__main__":
print("Hallo Gallo")
print(baseName)
files = os.listdir(baseName)
c = 1
for file in files:
print(file)
try:
plan = dicom.read_file(baseName + "/" + file)
plt.subplot(5, 5, c)
pix = plan.pixel_array
print(plan.InstanceNumber)
plt.title("In Num " + str(plan.InstanceNumber))
plt.imshow(pix)
c += 1
except:
print "Unexpected error:", sys.exc_info()[0]
plt.draw()
plt.waitforbuttonpress()
def _read_dicom_image(self, filename):
d = dicom.read_file(filename)
img = d.pixel_array
return np.array(img)
def load_by_type(path, file_type, contains=""):
return [
dicom.read_file(os.path.join(path, s)) for s in os.listdir(path)
if s.startswith(file_type) and (contains in s)
]
def loadPhilips4DUSAsSequence(self, loadable):
"""Load the selection as an Ultrasound, store in a Sequence node
"""
# get the key info from the "fake" dicom file
filePath = loadable.files[0]
ds = dicom.read_file(filePath, stop_before_pixels=True)
columns = ds.Columns
rows = ds.Rows
slices = ds[(0x3001, 0x1001)].value # private tag!
spacing = (
ds.PhysicalDeltaX * 10,
ds.PhysicalDeltaY * 10,
ds[(0x3001, 0x1003)].value * 10 # private tag!
)
frames = int(ds.NumberOfFrames)
imageComponents = frames
frameTimeMsec = ds.FrameTime
pixelShape = (frames, slices, rows, columns)
pixelSize = reduce(lambda x, y: x * y, pixelShape)
totalFileSize = os.path.getsize(filePath)
headerSize = totalFileSize - pixelSize
outputSequenceNode = slicer.vtkMRMLSequenceNode()
for frame in range(frames):
imgReader = vtk.vtkImageReader()
imgReader.SetFileDimensionality(3)
imgReader.SetFileName(filePath)
imgReader.SetNumberOfScalarComponents(1)
imgReader.SetDataScalarTypeToUnsignedChar()
imgReader.SetDataExtent(0, columns - 1, 0, rows - 1, 0, slices - 1)
imgReader.SetHeaderSize(headerSize +
frame * slices * rows * columns)
imgReader.FileLowerLeftOn()
imgReader.Update()
outputNode = slicer.vtkMRMLScalarVolumeNode()
outputNode.SetAndObserveImageData(imgReader.GetOutput())
outputNode.SetSpacing(spacing)
timeStampSec = "{:.3f}".format(frame * frameTimeMsec * 0.001)
outputSequenceNode.SetDataNodeAtValue(outputNode, timeStampSec)
outputSequenceNode.SetName(
slicer.mrmlScene.GenerateUniqueName(loadable.name))
slicer.mrmlScene.AddNode(outputSequenceNode)
# Create storage node that allows saving node as nrrd
outputSequenceStorageNode = slicer.vtkMRMLVolumeSequenceStorageNode()
slicer.mrmlScene.AddNode(outputSequenceStorageNode)
outputSequenceNode.SetAndObserveStorageNodeID(
outputSequenceStorageNode.GetID())
if not hasattr(loadable,
'createBrowserNode') or loadable.createBrowserNode:
# Add a browser node and show the volume in the slice viewer for user convenience
outputSequenceBrowserNode = slicer.vtkMRMLSequenceBrowserNode()
outputSequenceBrowserNode.SetName(
slicer.mrmlScene.GenerateUniqueName(
outputSequenceNode.GetName() + ' browser'))
slicer.mrmlScene.AddNode(outputSequenceBrowserNode)
outputSequenceBrowserNode.SetAndObserveMasterSequenceNodeID(
outputSequenceNode.GetID())
masterOutputNode = outputSequenceBrowserNode.GetProxyNode(
outputSequenceNode)
# Automatically select the volume to display
appLogic = slicer.app.applicationLogic()
selNode = appLogic.GetSelectionNode()
selNode.SetReferenceActiveVolumeID(masterOutputNode.GetID())
appLogic.PropagateVolumeSelection()
appLogic.FitSliceToAll()
slicer.modules.sequencebrowser.setToolBarActiveBrowserNode(
outputSequenceBrowserNode)
# create Subject hierarchy nodes for the loaded series
self.addSeriesInSubjectHierarchy(loadable, masterOutputNode)
return outputSequenceNode
# continue
# print ("Up folder name ", i)
if os.path.isdir(path + "/" + i):
print("Current folder ", (path + "/" + i))
for fname in os.listdir(path + "/" + i):
if fname.endswith(tuple(f_ext)):
next_level = path + "/" + i + "/" + fname
break
splitup = next_level.split('/')
list_no = len(os.listdir(path + "/" + i))
print("Number of files", list_no)
dcmhdr = dicom.read_file(next_level)
filenum = int(dcmhdr['0020', '0011'].value)
filename = dcmhdr['0008', '103e'].value
#TR = dcmhdr['0018', '0080'].value # Repetition Time
#TE = dcmhdr['0018', '0081'].value # Echo Time
# filename given example: fMRI_Resting_1_AP, T1W_MPR
print("filename", filename)
c_folder.append(filename)
#print ("Repetition Time TR ", TR)
#print ("Echo Time TE ", TE)
# DICOM directory name (long number)
mapoutname = str(splitup[6])
print("folder number", mapoutname)
"""
for dir_name, subdir_list, file_list in os.walk(path):
for filename in file_list:
if ".dcm" in filename.lower():
print filename
if "ct" in dir_name.lower():
ct_files.append(os.path.join(dir_name,filename))
if "rtst" in dir_name.lower():
rtst_files.append(os.path.join(dir_name,filename))
if 1:
print 'Extracting structure labels...',
sys.stdout.flush()
f = open('structure.dat','w')
sys.stdout.flush()
for file in rtst_files:
dcm_data = dicom.read_file(file)
patient_id = dcm_data[0x10, 0x20].value
structure_set_roi_sequence = dcm_data[0x3006,0x20].value
for i, structure_set_roi in enumerate(structure_set_roi_sequence):
if structure_set_roi[0x3006, 0x0022].value != i+1:
print 'Script cannot accomodate your dicom data. Exiting now.'
exit()
structure_line = patient_id+'|'+'|'.join( [ elem[0x3006,0x26].value for elem in structure_set_roi_sequence ])
f.write(structure_line+'\n')
print 'DONE'
sys.stdout.flush()
f.close()
if 1:
print 'Extracting slice data...'
sys.stdout.flush()