File size: 7,613 Bytes
7747544
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
"""
HNE2Cell — Step 2: Patch Extraction

Extract overlapping patches from color-normalized H&E images for cell detection.
Supports both 20x and 40x magnification (40x recommended for best results).

Usage:
    # 40x (recommended)
    python patchify.py \
        --input_dir /path/to/slides \
        --patch_size 256 \
        --overlap 64 \
        --magnification 40 \
        --workers 8

    # 20x (supported but 40x preferred)
    python patchify.py \
        --input_dir /path/to/slides \
        --patch_size 256 \
        --overlap 64 \
        --magnification 20 \
        --workers 8

Notes:
    - 40x magnification is recommended for optimal cell detection accuracy.
    - 20x is supported and functional, but fine-grained cell boundaries
      (especially small immune cells) may be less precise.
    - Input: Aligned-hne.tif (output of normalize.py)
    - Output: <section>/patches_<mag>x_p<patch>_o<overlap>/<name>_<x>_<y>.png
"""

import os
import argparse
import glob
import time
from multiprocessing import Pool

import numpy as np
from PIL import Image
from tqdm import tqdm

Image.MAX_IMAGE_PIXELS = None


# ========================== Utility functions ==============================


def black_to_white(pil_img: Image.Image) -> Image.Image:
    """Replace pure-black (0,0,0) pixels with white — avoids dark-border artifacts."""
    arr = np.array(pil_img)
    if arr.ndim == 3 and arr.shape[2] >= 3:
        mask = (arr[..., :3] == 0).all(axis=-1)
        arr[mask] = 255
    return Image.fromarray(arr)


def make_start_positions(length: int, patch_size: int, stride: int) -> list[int]:
    """Generate start positions so the last patch always reaches the edge."""
    if length < patch_size:
        return [0]
    starts = list(range(0, length - patch_size + 1, stride))
    last = length - patch_size
    if starts[-1] != last:
        starts.append(last)
    return starts


# ========================== Core patching ==================================


def extract_patches(
    image_path: str,
    output_dir: str,
    patch_size: int = 256,
    overlap: int = 64,
    prefix: str = "patch",
) -> int:
    """Crop overlapping patches from a single image and save as PNG.

    Returns the number of patches saved.
    """
    os.makedirs(output_dir, exist_ok=True)

    stride = patch_size - overlap
    assert stride > 0, f"overlap ({overlap}) must be < patch_size ({patch_size})"

    img = Image.open(image_path).convert("RGB")
    width, height = img.size

    xs = make_start_positions(width, patch_size, stride)
    ys = make_start_positions(height, patch_size, stride)

    count = 0
    with tqdm(total=len(xs) * len(ys), desc=prefix, unit="patch", leave=False) as pbar:
        for x0 in xs:
            for y0 in ys:
                patch = img.crop((x0, y0, x0 + patch_size, y0 + patch_size))
                patch = black_to_white(patch)
                patch.save(
                    os.path.join(output_dir, f"{prefix}_{x0}_{y0}.png"),
                    format="PNG",
                )
                count += 1
                pbar.update(1)
    return count


# =================== Per-section processing (for Pool) =====================

# These will be set once in main() before the pool is created
_ARGS = {}


def _process_section(section_dir: str) -> str:
    """Process a single section directory. Designed for multiprocessing.Pool."""

    patch_size = _ARGS["patch_size"]
    overlap = _ARGS["overlap"]
    magnification = _ARGS["magnification"]
    input_filename = _ARGS["input_filename"]

    # Locate input file
    candidates = [
        os.path.join(section_dir, f"{input_filename}.tif"),
        os.path.join(section_dir, f"{input_filename}.tiff"),
    ]
    image_path = next((p for p in candidates if os.path.exists(p)), None)

    if image_path is None:
        return f"[SKIP] {section_dir}: {input_filename}.tif not found"

    stride = patch_size - overlap
    out_dir = os.path.join(
        section_dir,
        f"patches_{magnification}x_p{patch_size}_o{overlap}",
    )

    section_name = os.path.basename(section_dir)

    t0 = time.time()
    n = extract_patches(
        image_path=image_path,
        output_dir=out_dir,
        patch_size=patch_size,
        overlap=overlap,
        prefix=section_name,
    )
    dt = time.time() - t0

    return (
        f"[OK] {section_name} | {magnification}x | "
        f"stride={stride} | {n} patches | {dt:.1f}s → {out_dir}"
    )


# =============================== CLI =======================================


def main():
    parser = argparse.ArgumentParser(
        description="Extract overlapping patches from normalized H&E images"
    )
    parser.add_argument(
        "--input_dir",
        type=str,
        required=True,
        help="Root directory containing section folders with Aligned-hne.tif files",
    )
    parser.add_argument(
        "--input_filename",
        type=str,
        default="Aligned-hne",
        help="Base filename of the normalized image (default: Aligned-hne)",
    )
    parser.add_argument(
        "--patch_size", type=int, default=256, help="Patch size in pixels (default: 256)"
    )
    parser.add_argument(
        "--overlap", type=int, default=64, help="Overlap in pixels (default: 64)"
    )
    parser.add_argument(
        "--magnification",
        type=int,
        default=40,
        choices=[20, 40],
        help="Slide magnification. 40x recommended; 20x supported. (default: 40)",
    )
    parser.add_argument(
        "--pattern",
        type=str,
        default="*",
        help="Glob pattern to match section folders (default: '*')",
    )
    parser.add_argument(
        "--workers", type=int, default=8, help="Number of parallel workers (default: 8)"
    )

    args = parser.parse_args()

    if args.magnification == 20:
        print(
            "⚠️  20x magnification is supported but 40x is recommended for best "
            "cell detection accuracy (especially small immune cells)."
        )

    # Collect section directories
    section_dirs = sorted(
        p
        for p in glob.glob(os.path.join(args.input_dir, args.pattern))
        if os.path.isdir(p)
    )

    if not section_dirs:
        # Maybe input_dir itself contains the image directly
        candidates = [
            os.path.join(args.input_dir, f"{args.input_filename}.tif"),
            os.path.join(args.input_dir, f"{args.input_filename}.tiff"),
        ]
        if any(os.path.exists(c) for c in candidates):
            section_dirs = [args.input_dir]
        else:
            raise SystemExit(
                f"No section folders matching '{args.pattern}' found in {args.input_dir}"
            )

    print(f"Found {len(section_dirs)} section(s) | {args.magnification}x | "
          f"patch={args.patch_size} overlap={args.overlap}")

    # Set global args for worker processes
    global _ARGS
    _ARGS = {
        "patch_size": args.patch_size,
        "overlap": args.overlap,
        "magnification": args.magnification,
        "input_filename": args.input_filename,
    }

    if args.workers <= 1 or len(section_dirs) == 1:
        results = [_process_section(d) for d in tqdm(section_dirs, desc="Sections")]
    else:
        with Pool(processes=min(args.workers, len(section_dirs))) as pool:
            results = list(
                tqdm(
                    pool.imap_unordered(_process_section, section_dirs),
                    total=len(section_dirs),
                    desc="Sections",
                )
            )

    print("\n".join(results))


if __name__ == "__main__":
    main()