Misc features

docs/Usage/Preprocessing.md

@@ -51,11 +51,11 @@ tomo_preprocessing <command> --help
 
 
 - **match_pixel_size**: Tomogram rescaling to specified pixel size. Example:  
-`tomo_preprocessing match_pixel_size --input_tomogram <path-to-tomo> --output_path <path-to-output> --pixel_size_out 10.0 --pixel_size_in <your-px-size>`
+`tomo_preprocessing match_pixel_size --input-tomogram <path-to-tomo> --output-path <path-to-output> --pixel-size-out 10.0 --pixel-size-in <your-px-size>`
 - **match_seg_to_tomo**: Segmentation rescaling to fit to target tomogram's shape. Example:  
-`tomo_preprocessing match_seg_to_tomo --seg_path <path-to-seg> --orig_tomo_path <path-to-tomo> --output_path <path-to-output>`
+`tomo_preprocessing match_seg_to_tomo --seg-path <path-to-seg> --orig-tomo-path <path-to-tomo> --output-path <path-to-output>`
 - **extract_spectrum**: Extracts the radially averaged amplitude spectrum from the input tomogram. Example:  
-`tomo_preprocessing extract_spectrum --input_path <path-to-tomo> --output_path <path-to-output>`
+`tomo_preprocessing extract_spectrum --input-path <path-to-tomo> --output-path <path-to-output>`
 - **match_spectrum**: Match amplitude of Fourier spectrum from input tomogram to target spectrum. Example:  
 `tomo_preprocessing match_spectrum --input <path-to-tomo> --target <path-to-spectrum> --output <path-to-output>`
 
@@ -64,18 +64,18 @@ tomo_preprocessing <command> --help
 Pixel size matching is recommended when your tomogram pixel sizes differs strongly from the training pixel size range (roughly 10-14&Aring;). You can perform it using the command
 
 ```shell
-tomo_preprocessing match_pixel_size --input_tomogram <path-to-tomo> --output_path <path-to-output> --pixel_size_out 10.0 --pixel_size_in <your-px-size>
+tomo_preprocessing match_pixel_size --input-tomogram <path-to-tomo> --output-path <path-to-output> --pixel-size-out 10.0 --pixel-size-in <your-px-size>
 ```
 
 after adjusting the paths to your respective tomograms.
-Afterwards, you can perform MemBrain's segmentation on the rescaled tomogram (i.e. the one specified in `--output_path`).  
+Afterwards, you can perform MemBrain's segmentation on the rescaled tomogram (i.e. the one specified in `--output-path`).  
 Now, this new segmentation does not have the same shape as the original non-pixel-size-matched tomogram. To rescale the new segmentation to the original tomogram again, you can use
 
 ```shell
-tomo_preprocessing match_seg_to_tomo --seg_path <path-to-seg> --orig_tomo_path <path-to-tomo> --output_path <path-to-output>
+tomo_preprocessing match_seg_to_tomo --seg_path <path-to-seg> --orig-tomo-path <path-to-tomo> --output-path <path-to-output>
 ```
 
-where the `--seg_path`is the segmentation created by MemBrain and the `--orig_tomo_path`is the original tomogram before rescaling to the new pixel size.  
+where the `--seg-path`is the segmentation created by MemBrain and the `--orig-tomo-path`is the original tomogram before rescaling to the new pixel size.  
 The output of this function will be MemBrain's segmentation, but matched to the pixel size of the original tomogram.
 
 
@@ -84,7 +84,7 @@ Fourier amplitude matching is performed in two steps:
 
 1. Extraction of the target Fourier spectrum:  
 ```shell
-tomo_preprocessing extract_spectrum --input_path <path-to-tomo> --output_path <path-to-output>
+tomo_preprocessing extract_spectrum --input-path <path-to-tomo> --output-path <path-to-output>
 ```  
 This extracts the radially averaged Fourier spectrum and stores it into a .tsv file.
 2. Matching of the input tomogram to the extracted spectrum:  

docs/Usage/Segmentation.md

@@ -83,6 +83,10 @@ You can also compute the connected components [after you have segmented your tom
 
 **--connected-component-thres**: Threshold for connected components. Components smaller than this will be removed from the segmentation. [default: None]
 
+**--test-time-augmentation / --no-test-time-augmentation**: Should 8-fold test time augmentation be used? If activated (default), segmentations tendo be slightly better, but runtime is increased.
+
+**--segmentation-threshold**: Set a custom threshold for thresholding your membrane scoremap to increase / decrease segmented membranes (default: 0.0).
+
 **--sliding-window-size** INTEGER Sliding window size used for inference. Smaller values than 160 consume less GPU, but also lead to worse segmentation results! [default: 160] 
 
 **--help** Show this message and exit.     
@@ -102,10 +106,17 @@ If you have segmented your tomograms already, but would still like to extract th
 ```shell
 membrain components --segmentation-path <path-to-your-segmentation> --connected-component-thres 50 --out-folder <folder-to-store-components>
 ```
-
 ### Note: 
 Computing the connected components, and particularly also removing the small components can be quite compute intensive and take a while.
 
+## Custom thresholding
+In some cases, the standard threshold ($0.0$) may not be the ideal value for segmenting your tomograms. In order to explore what threshold may be best, you can use the above segmentation command with the flag `--store-probabilities`. This will store a membrane scoremap that you can threshold using different values using the command:
+
+```
+membrain thresholds --scoremap-path <path-to-scoremap>
+        --thresholds -1.5 --thresholds -0.5 --thresholds 0.0 --thresholds 0.5
+```
+In this way, you can pass as many thresholds as you would like and the function will output one segmentation for each.
 
 
 ## Post-Processing

src/membrain_seg/annotations/extract_patches.py

@@ -193,7 +193,7 @@ def extract_patches(
                 min_coords[0] : min_coords[0] + 160,
                 min_coords[1] : min_coords[1] + 160,
                 min_coords[2] : min_coords[2] + 160,
-            ]
+            ].copy()
             cur_patch_labels = pad_labels(
                 cur_patch_labels, padding, pad_value=pad_value
             )

src/membrain_seg/annotations/merge_corrections.py

@@ -40,20 +40,25 @@ def get_corrections_from_folder(folder_name, orig_pred_file):
     for filename in os.listdir(folder_name):
         if not (
             filename.startswith("Add")
+            or filename.startswith("add")
             or filename.startswith("Remove")
+            or filename.startswith("remove")
             or filename.startswith("Ignore")
+            or filename.startswith("ignore")
         ):
             print("ATTENTION! Not processing", filename)
             print("Is this intended?")
             continue
         readdata = sitk.GetArrayFromImage(
             sitk.ReadImage(os.path.join(folder_name, filename))
         )
-        if filename.startswith("Add"):
+        print("Adding file", filename, "<--")
+
+        if filename.startswith("Add") or filename.startswith("add"):
             add_patch += readdata
-        if filename.startswith("Remove"):
+        if filename.startswith("Remove") or filename.startswith("remove"):
             remove_patch += readdata
-        if filename.startswith("Ignore"):
+        if filename.startswith("Ignore") or filename.startswith("ignore"):
             ignore_patch += readdata
         correction_count += 1
 
@@ -112,6 +117,8 @@ def convert_single_nrrd_files(labels_dir, corrections_dir, out_dir):
             token = label_file[:-7]
         elif label_file.endswith(".nrrd"):
             token = label_file[:-5]
+        elif label_file.endswith(".mrc"):
+            token = label_file[:-4]
         found_flag = 0
         for filename in os.listdir(corrections_dir):
             if not os.path.isdir(os.path.join(corrections_dir, filename)):
@@ -121,7 +128,7 @@ def convert_single_nrrd_files(labels_dir, corrections_dir, out_dir):
                 merged_corrections = get_corrections_from_folder(
                     cur_patch_corrections_folder, os.path.join(labels_dir, label_file)
                 )
-                out_file = os.path.join(out_dir, label_file)
+                out_file = os.path.join(out_dir, token + ".nii.gz")
                 print("Storing corrections in", out_file)
                 write_nifti(out_file, merged_corrections)
                 found_flag = 1

src/membrain_seg/segmentation/cli/segment_cli.py

@@ -1,4 +1,5 @@
 import os
+from typing import List
 
 from typer import Option
 
@@ -37,6 +38,17 @@ def segment(
         help="Threshold for connected components. Components smaller than this will \
             be removed from the segmentation.",
     ),
+    test_time_augmentation: bool = Option(  # noqa: B008
+        True,
+        help="Use 8-fold test time augmentation (TTA)? TTA improves segmentation \
+        quality slightly, but also increases runtime.",
+    ),
+    segmentation_threshold: float = Option(  # noqa: B008
+        0.0,
+        help="Threshold for the membrane segmentation. Only voxels with a \
+            membrane score higher than this threshold will be segmented. \
+                (default: 0.0)",
+    ),
     sliding_window_size: int = Option(  # noqa: B008
         160,
         help="Sliding window size used for inference. Smaller values than 160 \
@@ -58,6 +70,8 @@ def segment(
         store_connected_components=store_connected_components,
         connected_component_thres=connected_component_thres,
         sw_roi_size=sliding_window_size,
+        test_time_augmentation=test_time_augmentation,
+        segmentation_threshold=segmentation_threshold,
     )
 
 
@@ -95,3 +109,53 @@ def components(
         os.path.splitext(os.path.basename(segmentation_path))[0] + "_components.mrc",
     )
     store_tomogram(filename=out_file, tomogram=segmentation)
+
+
+@cli.command(name="thresholds", no_args_is_help=True)
+def thresholds(
+    scoremap_path: str = Option(  # noqa: B008
+        help="Path to the membrane scoremap to be processed.", **PKWARGS
+    ),
+    thresholds: List[float] = Option(  # noqa: B008
+        ...,
+        help="List of thresholds. Provide multiple by repeating the option.",
+    ),
+    out_folder: str = Option(  # noqa: B008
+        "./predictions",
+        help="Path to the folder where thresholdedsegmentations \
+            should be stored.",
+    ),
+):
+    """Process the provided scoremap using given thresholds.
+
+    Given a membrane scoremap, this function thresholds the scoremap data
+    using the provided threshold(s). The thresholded scoremaps are then stored
+    in the specified output folder. If multiple thresholds are provided,
+    separate thresholded scoremaps will be generated for each threshold.
+
+    Example
+    -------
+    membrain thresholds --scoremap-path <path-to-scoremap>
+        --thresholds -1.5 --thresholds -0.5 --thresholds 0.0 --thresholds 0.5
+
+    This will generate thresholded scoremaps for the provided scoremap at
+    thresholds -1.5, -0.5, 0.0 and 0.5.The results will be saved with filenames
+    indicating the threshold values in the default 'predictions' folder or
+    in the folder specified by the user.
+    """
+    scoremap = load_tomogram(scoremap_path)
+    score_data = scoremap.data
+    if not isinstance(thresholds, list):
+        thresholds = [thresholds]
+    for threshold in thresholds:
+        print("Thresholding at", threshold)
+        thresholded_data = score_data > threshold
+        segmentation = scoremap
+        segmentation.data = thresholded_data
+        out_file = os.path.join(
+            out_folder,
+            os.path.splitext(os.path.basename(scoremap_path))[0]
+            + f"_threshold_{threshold}.mrc",
+        )
+        store_tomogram(filename=out_file, tomogram=segmentation)
+        print("Saved thresholded scoremap to", out_file)

src/membrain_seg/segmentation/dataloading/data_utils.py

@@ -131,6 +131,7 @@ def store_segmented_tomograms(
     connected_component_thres: int = None,
     mrc_header: np.recarray = None,
     voxel_size: float = None,
+    segmentation_threshold: float = 0.0,
 ) -> None:
     """
     Helper function for storing output segmentations.
@@ -163,6 +164,8 @@ def store_segmented_tomograms(
     voxel_size: float, optional
         If given, this will be the voxel size stored in the header of the
         output segmentation.
+    segmentation_threshold : float, optional
+        Threshold for the segmentation. Default is 0.0.
     """
     # Create out directory if it doesn't exist yet
     make_directory_if_not_exists(out_folder)
@@ -178,7 +181,9 @@ def store_segmented_tomograms(
             data=predictions_np, header=mrc_header, voxel_size=voxel_size
         )
         store_tomogram(out_file, out_tomo)
-    predictions_np_thres = predictions.squeeze(0).squeeze(0).cpu().numpy() > 0.0
+    predictions_np_thres = (
+        predictions.squeeze(0).squeeze(0).cpu().numpy() > segmentation_threshold
+    )
     out_file_thres = os.path.join(
         out_folder,
         os.path.basename(orig_data_path)[:-4] + "_" + ckpt_token + "_segmented.mrc",

src/membrain_seg/segmentation/segment.py

@@ -21,6 +21,7 @@ def segment(
     store_connected_components=False,
     connected_component_thres=None,
     test_time_augmentation=True,
+    segmentation_threshold=0.0,
 ):
     """
     Segment tomograms using a trained model.
@@ -55,6 +56,9 @@ def segment(
     test_time_augmentation: bool, optional
         If True, test-time augmentation is performed, i.e. data is rotated
         into eight different orientations and predictions are averaged.
+    segmentation_threshold: float, optional
+        Threshold for the membrane segmentation. Only voxels with a membrane
+        score higher than this threshold will be segmented. (default: 0.0)
 
     Returns
     -------
@@ -133,5 +137,6 @@ def segment(
         connected_component_thres=connected_component_thres,
         mrc_header=mrc_header,
         voxel_size=voxel_size,
+        segmentation_threshold=segmentation_threshold,
     )
     return segmentation_file