spacr 1.0.5__py3-none-any.whl → 1.0.7__py3-none-any.whl

This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
@@ -0,0 +1,384 @@
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+ %PDF-1.6
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+ 1 0 obj
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spacr/settings.py CHANGED
@@ -1022,7 +1022,7 @@ expected_types = {
1022
1022
 
1023
1023
  categories = {"Paths":[ "src", "grna", "barcodes", "custom_model_path", "dataset","model_path","grna_csv","row_csv","column_csv", "metadata_files", "score_data","count_data"],
1024
1024
  "General": ["cell_mask_dim", "cytoplasm", "cell_chann_dim", "cell_channel", "nucleus_chann_dim", "nucleus_channel", "nucleus_mask_dim", "pathogen_mask_dim", "pathogen_chann_dim", "pathogen_channel", "test_mode", "plot", "metadata_type", "custom_regex", "experiment", "channels", "magnification", "channel_dims", "apply_model_to_dataset", "generate_training_dataset", "train_DL_model", "delete_intermediate", "uninfected", ],
1025
- "Cellpose":["denoise","fill_in","from_scratch", "n_epochs", "width_height", "model_name", "custom_model", "resample", "rescale", "CP_prob", "flow_threshold", "percentiles", "invert", "diameter", "grayscale", "Signal_to_noise", "resize", "target_height", "target_width"],
1025
+ "Cellpose":["fill_in","from_scratch", "n_epochs", "width_height", "model_name", "custom_model", "resample", "rescale", "CP_prob", "flow_threshold", "percentiles", "invert", "diameter", "grayscale", "Signal_to_noise", "resize", "target_height", "target_width"],
1026
1026
  "Cell": ["cell_diamiter","cell_intensity_range", "cell_size_range", "cell_background", "cell_Signal_to_noise", "cell_CP_prob", "cell_FT", "remove_background_cell", "cell_min_size", "cytoplasm_min_size", "adjust_cells", "cells", "cell_loc"],
1027
1027
  "Nucleus": ["nucleus_diamiter","nucleus_intensity_range", "nucleus_size_range", "nucleus_background", "nucleus_Signal_to_noise", "nucleus_CP_prob", "nucleus_FT", "remove_background_nucleus", "nucleus_min_size", "nucleus_loc"],
1028
1028
  "Pathogen": ["pathogen_diamiter","pathogen_intensity_range", "pathogen_size_range", "pathogen_background", "pathogen_Signal_to_noise", "pathogen_CP_prob", "pathogen_FT", "pathogen_model", "remove_background_pathogen", "pathogen_min_size", "pathogens", "pathogen_loc", "pathogen_types", "pathogen_plate_metadata", ],
@@ -1039,7 +1039,7 @@ categories = {"Paths":[ "src", "grna", "barcodes", "custom_model_path", "dataset
1039
1039
  "Plot": ["split_axis_lims", "x_lim","log_x","log_y", "plot_control", "plot_nr", "examples_to_plot", "normalize_plots", "cmap", "figuresize", "plot_cluster_grids", "img_zoom", "row_limit", "color_by", "plot_images", "smooth_lines", "plot_points", "plot_outlines", "black_background", "plot_by_cluster", "heatmap_feature","grouping","min_max","cmap","save_figure"],
1040
1040
  "Timelapse": ["timelapse", "fps", "timelapse_displacement", "timelapse_memory", "timelapse_frame_limits", "timelapse_remove_transient", "timelapse_mode", "timelapse_objects", "compartments"],
1041
1041
  "Advanced": ["merge_edge_pathogen_cells", "test_images", "random_test", "test_nr", "test", "test_split", "normalize", "target_unique_count","threshold_multiplier", "threshold_method", "min_n","shuffle", "target_intensity_min", "cells_per_well", "nuclei_limit", "pathogen_limit", "background", "backgrounds", "schedule", "test_size","exclude","n_repeats","top_features", "model_type_ml", "model_type","minimum_cell_count","n_estimators","preprocess", "remove_background", "normalize", "lower_percentile", "merge_pathogens", "batch_size", "filter", "save", "masks", "verbose", "randomize", "n_jobs"],
1042
- "Beta": ["all_to_mip", "upscale", "upscale_factor", "consolidate", "distance_gaussian_sigma","use_sam_pathogen","use_sam_nucleus", "use_sam_cell"]
1042
+ "Beta": ["all_to_mip", "upscale", "upscale_factor", "consolidate", "distance_gaussian_sigma","use_sam_pathogen","use_sam_nucleus", "use_sam_cell", "denoise"]
1043
1043
  }
1044
1044
 
1045
1045
 
spacr/spacr_cellpose.py CHANGED
@@ -5,7 +5,6 @@ from cellpose import models as cp_models
5
5
  from IPython.display import display
6
6
  from multiprocessing import Pool
7
7
  from skimage.transform import resize as resizescikit
8
- from scipy.ndimage import binary_fill_holes
9
8
 
10
9
  def parse_cellpose4_output(output):
11
10
  """
spacr/utils.py CHANGED
@@ -1314,7 +1314,7 @@ def _get_cellpose_channels_v2(src, nucleus_channel, pathogen_channel, cell_chann
1314
1314
 
1315
1315
  return cellpose_channels
1316
1316
 
1317
- def _get_cellpose_channels(src, nucleus_channel, pathogen_channel, cell_channel):
1317
+ def _get_cellpose_channels_v1(src, nucleus_channel, pathogen_channel, cell_channel):
1318
1318
 
1319
1319
  cell_mask_path = os.path.join(src, 'masks', 'cell_mask_stack')
1320
1320
  nucleus_mask_path = os.path.join(src, 'masks', 'nucleus_mask_stack')
@@ -1346,6 +1346,56 @@ def _get_cellpose_channels(src, nucleus_channel, pathogen_channel, cell_channel)
1346
1346
 
1347
1347
  return cellpose_channels
1348
1348
 
1349
+ def _get_cellpose_channels(src, nucleus_channel, pathogen_channel, cell_channel):
1350
+ cell_mask_path = os.path.join(src, 'masks', 'cell_mask_stack')
1351
+ nucleus_mask_path = os.path.join(src, 'masks', 'nucleus_mask_stack')
1352
+ pathogen_mask_path = os.path.join(src, 'masks', 'pathogen_mask_stack')
1353
+
1354
+ if any(os.path.exists(p) for p in [cell_mask_path, nucleus_mask_path, pathogen_mask_path]):
1355
+ if any(c is None for c in [nucleus_channel, pathogen_channel, cell_channel]):
1356
+ print('Warning: Cellpose masks already exist. Unexpected behaviour if any channel is None while masks exist.')
1357
+
1358
+ # Enforced order: nucleus → cell → pathogen
1359
+ logical_order = []
1360
+ if nucleus_channel is not None:
1361
+ logical_order.append(('nucleus', nucleus_channel))
1362
+ if cell_channel is not None:
1363
+ logical_order.append(('cell', cell_channel))
1364
+ if pathogen_channel is not None:
1365
+ logical_order.append(('pathogen', pathogen_channel))
1366
+
1367
+ # Remove duplicate values while preserving first occurrence
1368
+ seen = set()
1369
+ ordered_channels = []
1370
+ for name, ch in logical_order:
1371
+ if ch not in seen:
1372
+ ordered_channels.append(ch)
1373
+ seen.add(ch)
1374
+
1375
+ # Map actual channel values to capped indices
1376
+ remap = {ch: min(i, 2) for i, ch in enumerate(ordered_channels)}
1377
+
1378
+ # Final channel assignments
1379
+ cellpose_channels = {}
1380
+
1381
+ if nucleus_channel is not None:
1382
+ c = remap[nucleus_channel]
1383
+ cellpose_channels['nucleus'] = [c, c]
1384
+
1385
+ if cell_channel is not None:
1386
+ c = remap[cell_channel]
1387
+ if nucleus_channel is not None:
1388
+ n = remap[nucleus_channel]
1389
+ cellpose_channels['cell'] = [n, c]
1390
+ else:
1391
+ cellpose_channels['cell'] = [c, c]
1392
+
1393
+ if pathogen_channel is not None:
1394
+ c = remap[pathogen_channel]
1395
+ cellpose_channels['pathogen'] = [c, c]
1396
+
1397
+ return cellpose_channels
1398
+
1349
1399
  def annotate_conditions(df, cells=None, cell_loc=None, pathogens=None, pathogen_loc=None, treatments=None, treatment_loc=None):
1350
1400
  """
1351
1401
  Annotates conditions in a DataFrame based on specified criteria and combines them into a 'condition' column.
@@ -1,6 +1,6 @@
1
1
  Metadata-Version: 2.1
2
2
  Name: spacr
3
- Version: 1.0.5
3
+ Version: 1.0.7
4
4
  Summary: Spatial phenotype analysis of crisp screens (SpaCr)
5
5
  Home-page: https://github.com/EinarOlafsson/spacr
6
6
  Author: Einar Birnir Olafsson