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View Code? Open in Web Editor NEWAn implementation of Unet for pytorch designed for digital pathology segmentation
License: MIT License
An implementation of Unet for pytorch designed for digital pathology segmentation
License: MIT License
i use this
ipdb> make_output_unet_cmd.py imgBF.tif --model epistroma_unet_best_model,pth
ipdb> make_output_unet_cmd.py *.tif --model epistroma_unet_best_model,pth
but it make error.
invaild syntax. how i can solve this.
tif file and pth file exist at same file
i use window
I used the project on your website from here and nuclei dataset on your dataset from here
after I made the pytable file by make_hdf5.py
patch_size=500 #size of the tiles to extract and save in the database, must be >= to training size
stride_size=250 #distance to skip between patches, 1 indicated pixel wise extraction, patch_size would result in non-overlapping tiles
mirror_pad_size=250 # number of pixels to pad *after* resize to image with by mirroring (edge's of patches tend not to be analyzed well, so padding allows them to appear more centered in the patch)
test_set_size=.1 # what percentage of the dataset should be used as a held out validation/testing set
resize=1 #resize input images
classes=[0,1] #
I train by train_unet.ipnb
but the error showed up
---------------------------------------------------------------------------
TypeError Traceback (most recent call last)
<ipython-input-13-a5149657a6ab> in <module>
16 model.eval() # Set model to evaluate mode
17
---> 18 for ii , (X, y, y_weight) in enumerate(dataLoader[phase]): #for each of the batches
19 X = X.to(device) # [Nbatch, 3, H, W]
20 y_weight = y_weight.type('torch.FloatTensor').to(device)
~\AppData\Local\Continuum\anaconda3\lib\site-packages\torch\utils\data\dataloader.py in __iter__(self)
191
192 def __iter__(self):
--> 193 return _DataLoaderIter(self)
194
195 def __len__(self):
~\AppData\Local\Continuum\anaconda3\lib\site-packages\torch\utils\data\dataloader.py in __init__(self, loader)
467 # before it starts, and __del__ tries to join but will get:
468 # AssertionError: can only join a started process.
--> 469 w.start()
470 self.index_queues.append(index_queue)
471 self.workers.append(w)
~\AppData\Local\Continuum\anaconda3\lib\multiprocessing\process.py in start(self)
110 'daemonic processes are not allowed to have children'
111 _cleanup()
--> 112 self._popen = self._Popen(self)
113 self._sentinel = self._popen.sentinel
114 # Avoid a refcycle if the target function holds an indirect
~\AppData\Local\Continuum\anaconda3\lib\multiprocessing\context.py in _Popen(process_obj)
221 @staticmethod
222 def _Popen(process_obj):
--> 223 return _default_context.get_context().Process._Popen(process_obj)
224
225 class DefaultContext(BaseContext):
~\AppData\Local\Continuum\anaconda3\lib\multiprocessing\context.py in _Popen(process_obj)
320 def _Popen(process_obj):
321 from .popen_spawn_win32 import Popen
--> 322 return Popen(process_obj)
323
324 class SpawnContext(BaseContext):
~\AppData\Local\Continuum\anaconda3\lib\multiprocessing\popen_spawn_win32.py in __init__(self, process_obj)
87 try:
88 reduction.dump(prep_data, to_child)
---> 89 reduction.dump(process_obj, to_child)
90 finally:
91 set_spawning_popen(None)
~\AppData\Local\Continuum\anaconda3\lib\multiprocessing\reduction.py in dump(obj, file, protocol)
58 def dump(obj, file, protocol=None):
59 '''Replacement for pickle.dump() using ForkingPickler.'''
---> 60 ForkingPickler(file, protocol).dump(obj)
61
62 #
~\AppData\Local\Continuum\anaconda3\lib\site-packages\tables\hdf5extension.cp37-win_amd64.pyd in tables.hdf5extension.Array.__reduce_cython__()
TypeError: self.dims,self.dims_chunk,self.maxdims cannot be converted to a Python object for pickling
what mistake did I make?
For data sets occasionally containing slides with too many regions or area > 4-byte INT_MAX, a runtime error will be reported from the lower level operations on PILs, while using cv2.imread.
In the script make_output_unet no picture is left after cropping away the padding if stride_size == patch_size.
Additionally, as padding with this setting was only applied at the outside, the inner pictures get cropped though nothing was padded here.
no edge is shown, although I would expect one. If I re - run the cell, sometimes an edge is shown, sometimes is not. Is this normal? I use edge_weight = 10 to help NN to separate better one region from the other. I apply the following transformations,
INPUT IMAGE TRANS
transforms.ToPILImage()
, transforms.RandomVerticalFlip()
, transforms.RandomHorizontalFlip()
# these need to be in a reproducible order, first affine transforms and then color
, transforms.RandomCrop(size=(patch_size,patch_size),pad_if_needed=True)
, transforms.RandomResizedCrop(size=patch_size)
, transforms.RandomAffine( 90, translate = (0.5, 0.5), scale = ( 0.5, 2.5))
, transforms.RandomRotation(180)
, transforms.ColorJitter(brightness=0, contrast=0, saturation=0, hue=.5)
, transforms.RandomGrayscale()
, transforms.ToTensor()
LABEL IMAGE TRANS
transforms.ToPILImage()
, transforms.RandomVerticalFlip()
, transforms.RandomHorizontalFlip()
# these need to be in a reproducible order, first affine transforms and then color
, transforms.RandomCrop( size = ( patch_size, patch_size), pad_if_needed = True)
, transforms.RandomResizedCrop( size = patch_size, interpolation = PIL.Image.NEAREST)
, transforms.RandomAffine( 90, translate = (0.5, 0.5), scale = ( 0.5, 2.5))
, transforms.RandomRotation( 180)
Thanks, happy July :)
Thank you for sharing this sophisticated script.
I got problems figuring out which exact changes to make in order to run it with data containing 7 classes of which I want to ignore the one containing background: first while making th hdf5 file and second during the training.
Is it possible you could explain the corresponding lines in detail?
E possivel rodar esse projeto no colab ?
The block_shape expect the mask to be 3-channel patches, while the squeeze operation only performs on the 1st channel only, which is also what is pushed into the h5 array.
I am loading my data into a pytable according to your code. Then, I am trying to train the U - net using your code as is. I get and IndexError: Index out of range at line
for ii, ( X, y, y_weight) in enumerate( dataLoader[ phase]):
How could I resolve this? When I am using the dataset[ phase] directly it works without any problem so far.
EDIT : I have solved the issue be resolving a bug in creating the pytable database. Previously the database was being created successfully without showing that bug. An indicator of the bug is when the amount of patch images is not the same as the amount of mask/label patch images.
Thanks.
Hi,
it appears that the slicing in numpy array would automatically remove the trailing singleton dimension.
The slice io_arr_out[:,:,:,0] is already npatches x patch_size x patch_size, given that the shape of io_arr_out is
npatches x patch_size x patch_size x 3 (for 3-channel inputs).
Also, in one of my slides, the annotated area without downsampling is already small enough, and the downsampled ROI yields a tile smaller than the patch_size, which makes its padded version of io_arr_out
to be 1x patch_size x patch_size x 3.
Using squeeze will incorrectly collapse the leading singleton dimension which we don't want to drop, and raise errors because the rank of the result will mismatch the rank of the hdf5 array.
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