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Copy pathPixelate3.py
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471 lines (399 loc) · 19.4 KB
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#!/usr/bin/env python3
##This is a flag.
Silent=False
##These are library imports. OS is for file manipulation
import os
##Numpy is for mathematical manipulation, especially with matrices
import numpy as np
##Matplotlib is for processing images into and out of python, and graphing
import matplotlib.pyplot as plt
import matplotlib.mlab as mlab
##Imports latex labels
from matplotlib import rc
#rc('font',**{'family':'sans-serif','sans-serif':['Helvetica']})
## for Palatino and other serif fonts use:
#rc('font',**{'family':'serif','serif':['Palatino']})
#rc('text', usetex=True)
##Scipy contains some elements used in image processing that are required here
import scipy.spatial as scspat
import scipy.ndimage as ndim
##This imports the statistics module from scipy
import scipy.stats as scstats
##Scikit image is a package which contains a large number of image processing functions
import skimage.io as skio
import skimage.morphology as skmorph
import skimage.filters as filt
import skimage.measure as skmeas
import skimage.feature as skfea
import skimage.segmentation as skseg
import skimage.draw as skdr
import skimage.color as skcol
import skimage.transform as sktrans
import csv
import math
import random as rd
##Imports my Voronoi Split Algorithm into a Module
import VorSplit
from math import log10, floor
import seaborn as sns
import itertools
##Sets the x and y pixel numbers for the mesh
xRes=100
yRes=100
def normedmean(arr,ax):
mean = np.mean(arr)
variance = np.var(arr)
sigma = np.sqrt(variance)
x = np.linspace(min(arr), max(arr), 100)
ax.plot(x, mlab.normpdf(x, mean, sigma))
def round_sig(x, sig=3):
return round(x, sig-int(floor(log10(abs(x))))-1)
##Defines paths to my directories and save file locations
path1=os.getcwd()
path0=os.path.dirname(path1)
path2=path0+ '/Output_Pixel_3'
ext='.eps'
##Creates list of paths to diabetes patients
lst0= ["T1D/"+f for f in os.listdir(path0+"/T1D")if (f.startswith('T'))]
lst1= ["T2D/"+f for f in os.listdir(path0+"/T2D")if (f.startswith('T'))]
lst2= ["Young_Onset/" + f for f in os.listdir(path0+"/Young_Onset" ) if ('CONTROL' in f.upper()) or ('CASE') in f.upper()]
##Zeroes all the sums of the types of patients (Sm)=sum (I)=Beta (T1D)=Type 1 Diabetes (CTL)=Control
## (S)=Delta (T2D)=Type 2 Diabetes
## (G)=Alpha (YO)=Young Onset
##This Loops Through the Patients
for PNum, f0 in enumerate(lst0+lst1+lst2):
##Sets the input and output paths for the count
ppaths=path0+'/'+f0
opaths=path2+'/'+f0
#print(ppaths)
if 'YOUNG' in ppaths.upper() and 'CONTROL' in ppaths.upper():
DAPIlst=[]
GCGlst=[]
INSlst=[]
SSTlst=[]
OALLlst=[]
for i in [f for f in os.listdir(ppaths)if f.startswith('Image')]:
DAPIlst+=[i+'/'+f for f in os.listdir(ppaths+'/'+i) if (f.endswith('.tif') and 'DAPI' in f.upper())]
GCGlst+=[i+'/'+f for f in os.listdir(ppaths+'/'+i) if (f.endswith('.tif') and 'GCG' in f.upper())]
INSlst+=[i+'/'+f for f in os.listdir(ppaths+'/'+i) if (f.endswith('.tif') and 'INS' in f.upper())]
SSTlst+=[i+'/'+f for f in os.listdir(ppaths+'/'+i) if (f.endswith('.tif') and 'SST' in f.upper())]
OALLlst+=[i+'/'+f for f in os.listdir(ppaths+'/'+i) if (f.endswith('.tif') and 'OVERLAY' in f.upper())]
elif 'YOUNG' in ppaths.upper() and 'CASE' in ppaths.upper():
DAPIlst=[]
GCGlst=[]
INSlst=[]
SSTlst=[]
OALLlst=[]
for i in [f for f in os.listdir(ppaths+'/ICI images/')if f.startswith('Image')]:
DAPIlst+=['/ICI images/'+i+'/'+f for f in os.listdir(ppaths+'/ICI images/'+i) if (f.endswith('.tif') and 'DAPI' in f.upper())]
GCGlst+=['/ICI images/'+i+'/'+f for f in os.listdir(ppaths+'/ICI images/'+i) if (f.endswith('.tif') and 'GCG' in f.upper())]
INSlst+=['/ICI images/'+i+'/'+f for f in os.listdir(ppaths+'/ICI images/'+i) if (f.endswith('.tif') and 'INS' in f.upper())]
SSTlst+=['/ICI images/'+i+'/'+f for f in os.listdir(ppaths+'/ICI images/'+i) if (f.endswith('.tif') and 'SST' in f.upper())]
OALLlst+=['/ICI images/'+i+'/'+f for f in os.listdir(ppaths+'/ICI images/'+i) if (f.endswith('.tif') and 'OVERLAY' in f.upper())]
# for i in [f for f in os.listdir(ppaths+'/IDI images/')if f.startswith('Image')]:
# DAPIlst+=['/IDI images/'+i+'/'+f for f in os.listdir(ppaths+'/IDI images/'+i) if (f.endswith('.tif') and 'DAPI' in f.upper())]
# GCGlst+=['/IDI images/'+i+'/'+f for f in os.listdir(ppaths+'/IDI images/'+i) if (f.endswith('.tif') and 'GCG' in f.upper())]
# INSlst+=['/IDI images/'+i+'/'+f for f in os.listdir(ppaths+'/IDI images/'+i) if (f.endswith('.tif') and 'INS' in f.upper())]
# SSTlst+=['/IDI images/'+i+'/'+f for f in os.listdir(ppaths+'/IDI images/'+i) if (f.endswith('.tif') and 'SST' in f.upper())]
# OALLlst+=['/IDI images/'+i+'/'+f for f in os.listdir(ppaths+'/IDI images/'+i) if (f.endswith('.tif') and 'OVERLAY' in f.upper())]
else:
##These return lists of the scans that have the different hormone stains
DAPIlst=[f for f in os.listdir(ppaths)if (f.endswith('.tif') and 'DAPI' in f.upper())]
GCGlst=[f for f in os.listdir(ppaths)if (f.endswith('.tif') and 'GCG' in f.upper())]
INSlst=[f for f in os.listdir(ppaths)if (f.endswith('.tif') and 'INS' in f.upper())]
SSTlst=[f for f in os.listdir(ppaths)if (f.endswith('.tif') and 'SST' in f.upper())]
OALLlst=[f for f in os.listdir(ppaths)if (f.endswith('.tif') and 'OVERLAY' in f.upper())]
##Creates string detailing the patients
pnt=f0.split("/")[-1]
#print(OALLlst)
#print('\n \n')
#continue
##Makes sure all the lists are consistent
if (any(len(lst) != len(DAPIlst) for lst in [GCGlst, INSlst, SSTlst])) or (DAPIlst == []):
print(f0)
print([[lst, len(lst)] for lst in [DAPIlst, GCGlst, INSlst, SSTlst, OALLlst]])
continue
if not os.path.exists(opaths):
os.makedirs(opaths)
##Set the patient Beta, Delta and Alpha cell count to zero
SmI0=0
SmS0=0
SmG0=0
ArrG1=[]
ArrI1=[]
ArrS1=[]
P_sm=[]
DAPIlst.sort(key=lambda x: x.split()[-1])
GCGlst.sort(key=lambda x: x.split()[-1])
INSlst.sort(key=lambda x: x.split()[-1])
SSTlst.sort(key=lambda x: x.split()[-1])
OALLlst.sort(key=lambda x: x.split()[-1])
##This loops through the Scans for the various patients
for num,(D,G,I,S,O) in enumerate(zip(DAPIlst,GCGlst, INSlst, SSTlst,OALLlst)):
##Set the scan Beta, Delta and Alpha cell count to zero, and make an image number string
SmI1=0
SmS1=0
SmG1=0
tst=D.split()[-1]
if ((D.split()[-1] != G.split()[-1]) or (D.split()[-1] != I.split()[-1]) or (D.split()[-1] != I.split()[-1]) or (D.split()[-1] != O.split()[-1]) ):
print(D.split()[-1] ,G.split()[-1] ,I.split()[-1] ,S.split()[-1] ,O.split()[-1] )
continue
nmbr=tst[:-4]
Dim=skio.imread(ppaths+'/'+D)
Gim=skio.imread(ppaths+'/'+G)
Iim=skio.imread(ppaths+'/'+I)
Sim=skio.imread(ppaths+'/'+S)
Oim=skio.imread(ppaths+'/'+O)
#print(Dim.shape)
##If silet is off, then plot this out
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Original overlay. Islet is: %s and patient is %s' %(nmbr,pnt))
ax.set_xlabel(r'X direction (pixels) $\rightarrow$ ')
ax.set_ylabel(r'$\leftarrow$ Y direction (pixels)', rotation='vertical')
ax=plt.imshow(Oim, interpolation='none')
plt.savefig(opaths+'/'+nmbr+'_Orig_Img'+ext, interpolation='none')
plt.close()
##Get rid of the backround blood
Sim1=Sim[:,:,0]+Sim[:,:,1]+Sim[:,:,2]
##Take the Laplacian of the Stomatostatin
##Get rid of the scale bar
DiffSim1=filt.laplace(Sim1)
##Get rid of scale bar
DiffSim1[-50:,-200:]=0
##Smooth it
DiffSim2=filt.gaussian(DiffSim1,1)
#Filter it
DiffSim3=DiffSim2>filt.threshold_triangle(DiffSim2)
##Mask the original image with the blood removed
Stcked=np.stack([DiffSim3,DiffSim3,DiffSim3],axis=2)
Sim=np.multiply(Stcked,Sim)
##If silet is off, then plot this out
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Islet Shape. Islet is: %s and patient is %s' %(nmbr,pnt))
ax.set_xlabel(r'X direction (pixels) $\rightarrow$ ')
ax.set_ylabel(r'$\leftarrow$ Y direction (pixels)', rotation='vertical')
ax=plt.imshow(DiffSim3, interpolation='none')
plt.savefig(opaths+'/'+nmbr+'_BloodFilt'+ext, interpolation='none')
plt.close()
##First thing is to find the islet shape. This can be done by adding the non Dapi, smoothing and thresholding
##Add together the three scans
IsltShp=Gim+Iim+Sim
##Add together the red blue and green to flatten the array
IsltShp0=IsltShp[:,:,0]+IsltShp[:,:,1]+IsltShp[:,:,2]
##Get rid of scale bar
IsltShp0[-50:,-200:]=0
##Gaussian smooth followed by a triangle filter to determine the boundary of the islets
IsltShp1=filt.gaussian(IsltShp0,10)
IsltShp2=IsltShp1>filt.threshold_triangle(IsltShp1)
##Get rid of any small objects that may yet exist
IsltShp3=skmorph.remove_small_holes(IsltShp2, connectivity=1, min_size=1000)
IsltShp4=skmorph.remove_small_objects(IsltShp3, connectivity=1, min_size=10000)
##If silent is off, then plot this out
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Islet Shape. Islet is: %s and patient is %s' %(nmbr,pnt))
ax.set_xlabel(r'X direction (pixels) $\rightarrow$ ')
ax.set_ylabel(r'$\leftarrow$ Y direction (pixels)', rotation='vertical')
ax=plt.imshow(IsltShp4, interpolation='none')
plt.savefig(opaths+'/'+nmbr+'_IsltShape'+ext, interpolation='none')
plt.close()
##Next is to find the Nuclei positions
##Flatten the arrays
Nuc=Dim[:,:,0]+Dim[:,:,1]+Dim[:,:,2]
##Get rid of scale bar
Nuc[-50:,-200:]=0
##Local threshold
NucPos=(Nuc>filt.threshold_local(Nuc, block_size=101))
##Fill the holes to make contingent nuclei
IsltNuc=np.multiply(NucPos,IsltShp4)
NucPos2=ndim.binary_fill_holes(IsltNuc)
##Mask the nuclei with the islet shape
##Remove small artefacts
NucPos3=skmorph.remove_small_holes(NucPos2, connectivity=1, min_size=1000)
NucPos4=skmorph.remove_small_objects(NucPos3, connectivity=1, min_size=100)
##Erode the image, to disentangle joint up DAPI stains
NucPos5=skmorph.erosion(NucPos4, selem=skmorph.disk(7))
##If silent is off, plot this out
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Nucleus position. Islet is: %s and patient is %s' %(nmbr,pnt))
ax.set_xlabel(r'X direction (pixels) $\rightarrow$ ')
ax.set_ylabel(r'$\leftarrow$ Y direction (pixels)', rotation='vertical')
ax=plt.imshow(NucPos5, interpolation='none')
plt.savefig(opaths+'/'+nmbr+'_Nuclei'+ext, interpolation='none')
plt.close()
##Label and number the nuclei
NucLabs,NucNum = skmeas.label(NucPos5, return_num=1)
P_sm.append(NucNum)
##Properties of regions assigned to an array
props=skmeas.regionprops(NucLabs)
##Make an array to store where the centers are
NPosArr=np.empty((NucNum,2))
##Loop through and save this
for c, p in enumerate(props):
NPosArr[c,0],NPosArr[c,1]=p.centroid
##Skip the rest of this loop in the unlikely event that there are no nuclei
if NucNum==0:
continue
##Do a voronoi split on the Islet and the points of the nuclei centres
canvas= VorSplit.VorSplt(NPosArr, IsltShp4.copy())
##Plot this if silent is off
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Cell Shape. Islet is: %s and patient is %s' %(nmbr,pnt))
ax.set_xlabel(r'X direction (pixels) $\rightarrow$ ')
ax.set_ylabel(r'$\leftarrow$ Y direction (pixels)', rotation='vertical')
ax=plt.imshow(canvas, interpolation='none')
plt.savefig(opaths+'/'+nmbr+'Cells'+ext, interpolation='none',cmap='gray')
plt.close()
##Labels the parts of the voronoi algorithm for the proporties array. 1 connectivity denotes the single line separating the cells
CellLab,CellNum = skmeas.label(canvas, return_num=1,connectivity=1,background=0)
##Get properties of the regions
props=skmeas.regionprops(CellLab)
##Flatten the scan arrays
IimF=Iim[:,:,0]+Iim[:,:,1]+Iim[:,:,2]
GimF=Gim[:,:,0]+Gim[:,:,1]+Gim[:,:,2]
SimF=Sim[:,:,0]+Sim[:,:,1]+Sim[:,:,2]
##Create an 8bit rbg canvas
Canvas1=np.zeros((Oim.shape[0],Oim.shape[1],3),dtype=np.uint8)
test_Canv=np.ones((Oim.shape[0],Oim.shape[1],3),dtype=np.uint8)
Canvas2=np.zeros((Oim.shape[0],Oim.shape[1],3),dtype=np.uint8)
IPosArr=[]
GPosArr=[]
SPosArr=[]
for p in props:
##Mask the insulin with the cells as defined by the Voronoi algorithm
CellI=np.multiply(p.image,IimF[p.bbox[0]:p.bbox[2],p.bbox[1]:p.bbox[3]])
CellG=np.multiply(p.image,GimF[p.bbox[0]:p.bbox[2],p.bbox[1]:p.bbox[3]])
CellS=np.multiply(p.image,SimF[p.bbox[0]:p.bbox[2],p.bbox[1]:p.bbox[3]])
tmpArr=np.round(np.array([p.centroid[0]*xRes/Oim.shape[0],p.centroid[1]*yRes/Oim.shape[1]])).astype(np.uint8)
##Calculate the total intensity of the scans within the defined cells
totI=np.sum(CellI)
totG=np.sum(CellG)
totS=3*np.sum(CellS)
##Compare these cells and evaluate accordingly
##Red is insulin
if totI>totG and totI>totS:
Canvas1[p.bbox[0]:p.bbox[2],p.bbox[1]:p.bbox[3],2]+=p.image
SmI0+=1
SmI1+=1
IPosArr.append(tmpArr)
##Red is glucagon
elif totG>totS:
Canvas1[p.bbox[0]:p.bbox[2],p.bbox[1]:p.bbox[3],0]+=p.image
SmG0+=1
SmG1+=1
GPosArr.append(tmpArr)
##Green is delta cells
else:
Canvas1[p.bbox[0]:p.bbox[2],p.bbox[1]:p.bbox[3],1]+=p.image
SmS0+=1
SmS1+=1
SPosArr.append(tmpArr)
ArrG1.append(SmG1)
ArrI1.append(SmI1)
ArrS1.append(SmS1)
##If Silent is off, then plot these cells
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Assigned cells. Alpha cells are red. Beta cells are blue.' + '\n' + r'Delta cells are green. Islet is: %s and patient is: %s' %(nmbr,pnt))
ax.set_xlabel(r'X direction (pixels) $\rightarrow$ ')
ax.set_ylabel(r'$\leftarrow$ Y direction (pixels)', rotation='vertical')
ax=plt.imshow(Canvas1*255, interpolation='none')
plt.savefig(opaths+'/'+nmbr+'_Assgned_Cells'+ext, interpolation='none',cmap='gray')
plt.close()
fracs=[SmI1,SmS1,SmG1]
str1, str2, str3=str(SmI1)+' Beta Cells',str(SmS1)+' Delta Cells',str(SmG1)+' Alpha Cells'
labels=[str1, str2, str3]
colors=['red','blue','green']
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Pie Chart Displaying the amount of cells.' +'\n' + r'Islet is: %s and patient is: %s' %(nmbr,pnt))
ax=plt.pie(fracs, labels=labels, colors=colors)
plt.savefig(opaths+'/'+nmbr+'_IsltPChart'+ext, interpolation='none')
plt.close()
##Reshape This Array to xres and yres
Canvas1=sktrans.resize(Canvas1,(xRes,yRes),order=0,mode="edge").astype(np.bool)
if Silent == False:
f, ax = plt.subplots()
ax.set_title(r'Pixelated cells. Alpha cells are red. Beta cells are blue.' + '\n' + r'Delta cells are green. Islet is: %s and patient is: %s' %(nmbr,pnt))
ax.set_xlabel(r'X direction (pixels) $\rightarrow$ ')
ax.set_ylabel(r'$\leftarrow$ Y direction (pixels)', rotation='vertical')
ax=plt.imshow(Canvas1, interpolation='none')
plt.savefig(opaths+'/'+nmbr+'_Pixelated_Cells'+ext, interpolation='none',cmap='gray')
plt.close()
##Need to find nearest neigbor pixels
GCList=[['g'] for x in range(len(GPosArr)) ]
SCList=[['s'] for x in range(len(SPosArr)) ]
ICList=[['i'] for x in range(len(IPosArr)) ]
for xx in range(xRes):
for yy in range(yRes):
#print(Canvas1[xx,yy])
if (Canvas1[xx,yy]==[0,0,0]).all():
continue
elif (Canvas1[xx,yy]==[1,0,0]).all():
mindist= xRes*yRes
for n,G in enumerate(GPosArr):
tmpdist = math.sqrt((xx-G[0])*(xx-G[0])+(yy-G[1])*(yy-G[1]))
if tmpdist<mindist:
mindist=tmpdist
ind=n
GCList[ind].append(xRes*yy+xx)
elif (Canvas1[xx,yy]==[0,1,0]).all():
mindist= xRes*yRes
for n,S in enumerate(SPosArr):
tmpdist = math.sqrt((xx-S[0])*(xx-S[0])+(yy-S[1])*(yy-S[1]))
if tmpdist<mindist:
mindist=tmpdist
ind=n
SCList[ind].append(xRes*yy+xx)
elif (Canvas1[xx,yy]==[0,0,1]).all():
mindist= xRes*yRes
for n,I in enumerate(IPosArr):
tmpdist = math.sqrt((xx-I[0])*(xx-I[0])+(yy-I[1])*(yy-I[1]))
if tmpdist<mindist:
mindist=tmpdist
ind=n
ICList[ind].append(xRes*yy+xx)
else:
print("Error. Value of array at point is " + str(Canvas1[xx,yy]))
for cenum, ce in enumerate(GCList):
GCList[cenum][1:]=sorted(ce[1:])
for cenum, ce in enumerate(SCList):
SCList[cenum][1:]=sorted(ce[1:])
for cenum, ce in enumerate(ICList):
ICList[cenum][1:]=sorted(ce[1:])
thefile = open(opaths+'/'+nmbr+'_Cells.txt', 'w+')
First=True
for item in GCList:
if len(item)<2:
continue
if First:
First=False
else:
thefile.write("\n")
for char in item:
thefile.write("%s " % char)
for item in SCList:
if len(item)<2:
continue
if First:
First=False
else:
thefile.write("\n")
for char in item:
thefile.write("%s " % char)
for item in ICList:
if len(item)<2:
continue
if First:
First=False
else:
thefile.write("\n")
for char in item:
thefile.write("%s " % char)
thefile.close()
print('Done for patient %s, %s of %s' %(f0, str(PNum),str(len(lst0+lst2+lst1)-1) ) )
print("done")