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import base64
import time
import cv2
import numpy as np
import torch
import torchvision.transforms as transforms
from PIL import Image
from pytorch_grad_cam import GradCAM
from pytorch_grad_cam.utils.model_targets import ClassifierOutputTarget
from pytorch_grad_cam.utils.image import show_cam_on_image
from model_loader import load_wbc_model, load_skin_model
# Class labels
WBC_CLASSES = ["Basophil", "Eosinophil", "Erythroblast", "IG", "Lymphocyte", "Monocyte", "Neutrophil", "Platelet"]
WBC_CLASSES_TF = ["Basophil", "Eosinophil", "Erythroblast", "IG", "Lymphocyte", "Monocyte", "Neutrophil", "Platelet", "RBC", "WBC", "Other"]
SKIN_CLASSES = [
"Benign keratosis-like lesions",
"Basal cell carcinoma",
"Actinic keratoses",
"Vascular lesions",
"Melanocytic nevi",
"Melanoma",
"Dermatofibroma"
]
# Image normalization parameters
IMAGE_SIZE = 224
NORM_MEAN = [0.485, 0.456, 0.406]
NORM_STD = [0.229, 0.224, 0.225]
def get_wbc_transforms():
return transforms.Compose([
transforms.Resize((IMAGE_SIZE, IMAGE_SIZE)),
transforms.ToTensor(),
transforms.Normalize(mean=NORM_MEAN, std=NORM_STD)
])
def generate_wbc_gradcam(model, input_tensor, target_class_idx, raw_image_np):
"""
Generates a Grad-CAM overlay for the WBC ResNet-18 model.
"""
try:
target_layers = [model[0][7][-1]]
cam = GradCAM(model=model, target_layers=target_layers)
targets = [ClassifierOutputTarget(target_class_idx)]
grayscale_cam = cam(input_tensor=input_tensor, targets=targets)[0, :]
rgb_img = cv2.resize(raw_image_np, (IMAGE_SIZE, IMAGE_SIZE)) / 255.0
cam_image = show_cam_on_image(rgb_img, grayscale_cam, use_rgb=True)
return cam_image
except Exception as e:
print(f"Error generating WBC Grad-CAM: {str(e)}")
return None
def generate_wbc_gradcam_tf(model, input_tensor, target_class_idx, raw_image_np):
"""
Generates a Grad-CAM overlay for the custom Keras WBC CNN model.
"""
try:
import tensorflow as tf
with tf.GradientTape() as tape:
x = tf.convert_to_tensor(input_tensor)
curr_x = x
conv_outputs = None
for layer in model.layers:
curr_x = layer(curr_x)
if isinstance(layer, tf.keras.layers.Conv2D):
conv_outputs = curr_x
predictions = curr_x
loss = predictions[:, target_class_idx]
if conv_outputs is None:
print("Error: No Conv2D layer found in Keras model.")
return None
grads = tape.gradient(loss, conv_outputs)
pooled_grads = tf.reduce_mean(grads, axis=(0, 1, 2))
conv_outputs_val = conv_outputs[0]
heatmap = conv_outputs_val @ pooled_grads[..., tf.newaxis]
heatmap = tf.squeeze(heatmap)
heatmap = tf.maximum(heatmap, 0.0)
max_val = tf.math.reduce_max(heatmap)
if max_val > 0:
heatmap = heatmap / max_val
heatmap = heatmap.numpy()
heatmap_resized = cv2.resize(heatmap, (128, 128))
rgb_img = cv2.resize(raw_image_np, (128, 128))
heatmap_color = cv2.applyColorMap(np.uint8(255 * heatmap_resized), cv2.COLORMAP_JET)
heatmap_color = cv2.cvtColor(heatmap_color, cv2.COLOR_BGR2RGB)
blend_image = cv2.addWeighted(rgb_img, 0.6, heatmap_color, 0.4, 0)
return blend_image
except Exception as e:
print(f"Error generating TensorFlow WBC Grad-CAM: {str(e)}")
return None
def generate_skin_attention_map(model, inputs, target_class_idx, raw_image_np):
"""
Generates a self-attention heatmap for the Vision Transformer skin cancer model.
"""
try:
with torch.no_grad():
outputs = model(**inputs, output_attentions=True)
attentions = outputs.attentions[-1]
mean_attn = attentions.mean(dim=1)[0]
cls_attn = mean_attn[0, 1:]
grid_size = int(np.sqrt(cls_attn.size(0)))
heatmap_grid = cls_attn.reshape(grid_size, grid_size).cpu().numpy()
heatmap_grid = (heatmap_grid - heatmap_grid.min()) / (heatmap_grid.max() - heatmap_grid.min() + 1e-8)
heatmap_resized = cv2.resize(heatmap_grid, (IMAGE_SIZE, IMAGE_SIZE))
heatmap_color = cv2.applyColorMap(np.uint8(255 * heatmap_resized), cv2.COLORMAP_JET)
heatmap_color = cv2.cvtColor(heatmap_color, cv2.COLOR_BGR2RGB)
rgb_img = cv2.resize(raw_image_np, (IMAGE_SIZE, IMAGE_SIZE))
blend_image = cv2.addWeighted(rgb_img, 0.6, heatmap_color, 0.4, 0)
return blend_image
except Exception as e:
print(f"Error generating Skin Attention Map: {str(e)}")
return None
def segment_cells(img_bgr, min_area=500):
lab = cv2.cvtColor(img_bgr, cv2.COLOR_BGR2LAB)
blur = cv2.GaussianBlur(lab[:,:,1],(7,7),0)
_,thresh = cv2.threshold(blur,0,255,
cv2.THRESH_BINARY_INV+cv2.THRESH_OTSU)
k = cv2.getStructuringElement(cv2.MORPH_ELLIPSE,(9,9))
cl = cv2.morphologyEx(thresh,cv2.MORPH_CLOSE,k,iterations=2)
cl = cv2.morphologyEx(cl,cv2.MORPH_OPEN,k,iterations=1)
cnts,_ = cv2.findContours(cl,cv2.RETR_EXTERNAL,
cv2.CHAIN_APPROX_SIMPLE)
boxes = []
for c in cnts:
if cv2.contourArea(c) < min_area: continue
x,y,w,h = cv2.boundingRect(c)
if 0.3 < w/max(h,1) < 3.0:
boxes.append((x,y,w,h))
return sorted(boxes, key=lambda b:b[2]*b[3], reverse=True)
def predict_image(image_bytes: bytes, filename: str, module_type: str):
"""
Performs inference and generates heatmaps.
"""
start_time = time.time()
try:
image = Image.open(io.BytesIO(image_bytes)).convert("RGB")
except Exception as e:
raise ValueError(f"Invalid image content: {str(e)}")
raw_image_np = np.array(image)
if module_type == "blood_cell":
wbc_model_data = load_wbc_model()
framework = wbc_model_data["framework"]
model = wbc_model_data["model"]
if framework == "tensorflow":
import tensorflow as tf
import matplotlib
matplotlib.use('Agg')
import matplotlib.pyplot as plt
from collections import Counter
# Setup class names list in the exact order as Colab training
CLASS_NAMES = ['basophil', 'eosinophil', 'erythroblast', 'ig', 'Lymphocyte',
'monocyte', 'neutrophil', 'platelet', 'RBC', 'WBC', 'other']
cmap_cls = plt.cm.tab10(np.linspace(0, 1, 11))
# Convert PIL image to BGR for OpenCV contour segmentation
img_bgr = cv2.cvtColor(raw_image_np, cv2.COLOR_RGB2BGR)
h, w = img_bgr.shape[:2]
# Run cell detection contours
# We use an adaptive threshold to handle small image dimensions (crops) as well
area_thresh = 100 if max(h, w) < 400 else 500
boxes = segment_cells(img_bgr, min_area=area_thresh)[:20] # Limit to top 20 cells
results = []
for (x, y, wb, hb) in boxes:
pad = 5
x1, y1 = max(0, x - pad), max(0, y - pad)
x2, y2 = min(img_bgr.shape[1], x + wb + pad), min(img_bgr.shape[0], y + hb + pad)
crop = img_bgr[y1:y2, x1:x2]
if crop.size == 0:
continue
# Preprocess crop (128x128, normalized RGB)
crop_rgb = cv2.cvtColor(crop, cv2.COLOR_BGR2RGB)
crop_128 = cv2.resize(crop_rgb, (128, 128))
crop_np = crop_128.astype(np.float32) / 255.0
input_tensor = np.expand_dims(crop_np, axis=0)
# Inference
preds = model(input_tensor, training=False)
probs = preds[0].numpy()
pred_idx = int(np.argmax(probs))
results.append({
'box': (x1, y1, x2, y2),
'label': WBC_CLASSES_TF[pred_idx],
'conf': float(probs[pred_idx]),
'probs': probs,
'crop': crop
})
if results:
# Draw bounding boxes and text
ann = img_bgr.copy()
for res in results:
x1, y1, x2, y2 = res['box']
i = WBC_CLASSES_TF.index(res['label'])
col = tuple(int(c*255) for c in cmap_cls[i][2::-1])
cv2.rectangle(ann, (x1, y1), (x2, y2), col, 2)
txt = f"{res['label']} {res['conf']*100:.1f}%"
(tw, th), _ = cv2.getTextSize(txt, cv2.FONT_HERSHEY_SIMPLEX, 0.4, 1)
cv2.rectangle(ann, (x1, y1 - th - 6), (x1 + tw + 4, y1), col, -1)
cv2.putText(ann, txt, (x1 + 2, y1 - 4), cv2.FONT_HERSHEY_SIMPLEX, 0.4, (255, 255, 255), 1, cv2.LINE_AA)
# Convert images to RGB for matplotlib
ann_rgb = cv2.cvtColor(ann, cv2.COLOR_BGR2RGB)
img_rgb = cv2.cvtColor(img_bgr, cv2.COLOR_BGR2RGB)
# Construct Colab-style matplotlib output figure
n = len(results)
n_cols = min(n, 5)
n_rows = (n + n_cols - 1) // n_cols
fig = plt.figure(figsize=(18, 5 + n_rows*3 + 4))
from matplotlib.gridspec import GridSpec
gs = GridSpec(3, 2, figure=fig,
height_ratios=[5, max(1, n_rows*3), 4],
hspace=0.5, wspace=0.3)
# Original Smear Plot
ax0 = fig.add_subplot(gs[0, 0])
ax0.imshow(img_rgb)
ax0.axis('off')
ax0.set_title('Original', fontweight='bold')
# Bounding Boxes Plot
ax1 = fig.add_subplot(gs[0, 1])
ax1.imshow(ann_rgb)
ax1.axis('off')
ax1.set_title(f'Detected: {n} cells', fontweight='bold')
# Cropped Cells Grid
sub = gs[1, :].subgridspec(n_rows, n_cols, hspace=0.7, wspace=0.35)
for idx_c, res in enumerate(results):
r, c = divmod(idx_c, n_cols)
ax = fig.add_subplot(sub[r, c])
cr = cv2.cvtColor(cv2.resize(res['crop'], (128, 128)), cv2.COLOR_BGR2RGB)
ax.imshow(cr)
col_idx = WBC_CLASSES_TF.index(res['label'])
col_plt = cmap_cls[col_idx]
ax.set_title(f"#{idx_c+1} {res['label']}\n{res['conf']*100:.1f}%",
fontsize=8, fontweight='bold', color=col_plt)
for sp in ax.spines.values():
sp.set_edgecolor(col_plt)
sp.set_linewidth(2)
ax.set_xticks([])
ax.set_yticks([])
# Confidence Score Bar Chart
ax3 = fig.add_subplot(gs[2, :])
lbls = [r['label'] for r in results]
confs = [r['conf']*100 for r in results]
bcols = [cmap_cls[WBC_CLASSES_TF.index(l)] for l in lbls]
bars = ax3.bar(range(n), confs, color=bcols, edgecolor='black', linewidth=0.5)
ax3.set_xticks(range(n))
ax3.set_xticklabels([f"#{i+1}\n{lbls[i]}" for i in range(n)], fontsize=8, rotation=30, ha='right')
ax3.set_ylabel('Confidence (%)')
ax3.set_ylim(0, 113)
ax3.axhline(40.0, color='red', ls='--', lw=1.2, label='Threshold (40%)')
ax3.legend(fontsize=9)
ax3.grid(axis='y', alpha=0.3)
ax3.set_title('Confidence per detected cell', fontweight='bold')
for bar, v in zip(bars, confs):
ax3.text(bar.get_x() + bar.get_width()/2, v + 1.5, f'{v:.1f}%', ha='center', fontsize=7, fontweight='bold')
# Summary Box at bottom
counts_cnt = Counter(lbls)
summary_str = " ".join([f"{cls}: {count}" for cls, count in sorted(counts_cnt.items())])
fig.text(0.5, 0.005, f"Cell count summary: {summary_str}",
ha='center', fontsize=11, fontweight='bold',
bbox=dict(boxstyle='round,pad=0.4', facecolor='lightyellow', edgecolor='orange'))
plt.suptitle(f'Results — {filename}', fontsize=13, fontweight='bold', y=1.01)
# Save figure to in-memory buffer
buf = io.BytesIO()
plt.savefig(buf, format='jpeg', dpi=120, bbox_inches='tight', facecolor='white')
buf.seek(0)
# Create base64 representation of the combined plot
base64_str = base64.b64encode(buf.read()).decode("utf-8")
plt.close(fig)
# Set prediction outputs
summary_label = ", ".join([f"{count} {cls}" for cls, count in counts_cnt.items()])
predicted_label = f"Detected {len(results)} cells: {summary_label}"
confidence = float(np.mean([res['conf'] for res in results]))
class_probabilities = {WBC_CLASSES_TF[i]: 0.0 for i in range(len(WBC_CLASSES_TF))}
for res in results:
class_probabilities[res['label']] += 1.0
for cls in class_probabilities:
class_probabilities[cls] /= len(results)
# Return the base64 plot directly back to the site
return predicted_label, confidence, class_probabilities, base64_str, time.time() - start_time
else:
# Fallback to single-cell prediction if no cells segmented
is_whole_smear = False
if not is_whole_smear:
img_128 = image.resize((128, 128))
img_np = np.array(img_128, dtype=np.float32) / 255.0
input_tensor = np.expand_dims(img_np, axis=0)
preds = model(input_tensor, training=False)
probs = preds[0].numpy()
pred_idx = int(np.argmax(probs))
confidence = float(probs[pred_idx])
predicted_label = WBC_CLASSES_TF[pred_idx]
class_probabilities = {WBC_CLASSES_TF[i]: float(probs[i]) for i in range(len(WBC_CLASSES_TF))}
heatmap_img = generate_wbc_gradcam_tf(model, input_tensor, pred_idx, raw_image_np)
else:
# Preprocess for PyTorch model
import matplotlib
matplotlib.use('Agg')
import matplotlib.pyplot as plt
from collections import Counter
# Setup class names list in the exact order as PyTorch training
CLASS_NAMES = ["Basophil", "Eosinophil", "Erythroblast", "IG", "Lymphocyte", "Monocyte", "Neutrophil", "Platelet"]
cmap_cls = plt.cm.tab10(np.linspace(0, 1, 8))
# Convert PIL image to BGR for OpenCV contour segmentation
img_bgr = cv2.cvtColor(raw_image_np, cv2.COLOR_RGB2BGR)
h, w = img_bgr.shape[:2]
# Run cell detection contours
# Using min_area=400 since that's what was used in the original notebook
area_thresh = 150 if max(h, w) < 400 else 400
boxes = segment_cells(img_bgr, min_area=area_thresh)[:20] # Limit to top 20 cells
results = []
transform = get_wbc_transforms()
for (x, y, wb, hb) in boxes:
pad = 5
x1, y1 = max(0, x - pad), max(0, y - pad)
x2, y2 = min(img_bgr.shape[1], x + wb + pad), min(img_bgr.shape[0], y + hb + pad)
crop = img_bgr[y1:y2, x1:x2]
if crop.size == 0:
continue
# Preprocess crop (transforms handles resizing to 224x224 and normalization)
crop_rgb = cv2.cvtColor(crop, cv2.COLOR_BGR2RGB)
crop_pil = Image.fromarray(crop_rgb)
input_tensor = transform(crop_pil).unsqueeze(0)
# PyTorch Inference
with torch.no_grad():
outputs = model(input_tensor)
probs = torch.softmax(outputs, dim=1)[0].cpu().numpy()
pred_idx = int(np.argmax(probs))
results.append({
'box': (x1, y1, x2, y2),
'label': CLASS_NAMES[pred_idx],
'conf': float(probs[pred_idx]),
'probs': probs,
'crop': crop
})
if results:
# Draw bounding boxes and text
ann = img_bgr.copy()
for res in results:
x1, y1, x2, y2 = res['box']
i = CLASS_NAMES.index(res['label'])
col = tuple(int(c*255) for c in cmap_cls[i][2::-1])
cv2.rectangle(ann, (x1, y1), (x2, y2), col, 2)
txt = f"{res['label']} {res['conf']*100:.1f}%"
(tw, th), _ = cv2.getTextSize(txt, cv2.FONT_HERSHEY_SIMPLEX, 0.4, 1)
cv2.rectangle(ann, (x1, y1 - th - 6), (x1 + tw + 4, y1), col, -1)
cv2.putText(ann, txt, (x1 + 2, y1 - 4), cv2.FONT_HERSHEY_SIMPLEX, 0.4, (255, 255, 255), 1, cv2.LINE_AA)
# Convert images to RGB for matplotlib
ann_rgb = cv2.cvtColor(ann, cv2.COLOR_BGR2RGB)
img_rgb = cv2.cvtColor(img_bgr, cv2.COLOR_BGR2RGB)
# Construct Colab-style matplotlib output figure
n = len(results)
n_cols = min(n, 5)
n_rows = (n + n_cols - 1) // n_cols
fig = plt.figure(figsize=(18, 5 + n_rows*3 + 4))
from matplotlib.gridspec import GridSpec
gs = GridSpec(3, 2, figure=fig,
height_ratios=[5, max(1, n_rows*3), 4],
hspace=0.5, wspace=0.3)
# Original Smear Plot
ax0 = fig.add_subplot(gs[0, 0])
ax0.imshow(img_rgb)
ax0.axis('off')
ax0.set_title('Original', fontweight='bold')
# Bounding Boxes Plot
ax1 = fig.add_subplot(gs[0, 1])
ax1.imshow(ann_rgb)
ax1.axis('off')
ax1.set_title(f'Detected: {n} cells', fontweight='bold')
# Cropped Cells Grid
sub = gs[1, :].subgridspec(n_rows, n_cols, hspace=0.7, wspace=0.35)
for idx_c, res in enumerate(results):
r, c = divmod(idx_c, n_cols)
ax = fig.add_subplot(sub[r, c])
cr = cv2.cvtColor(cv2.resize(res['crop'], (128, 128)), cv2.COLOR_BGR2RGB)
ax.imshow(cr)
col_idx = CLASS_NAMES.index(res['label'])
col_plt = cmap_cls[col_idx]
ax.set_title(f"#{idx_c+1} {res['label']}\n{res['conf']*100:.1f}%",
fontsize=8, fontweight='bold', color=col_plt)
for sp in ax.spines.values():
sp.set_edgecolor(col_plt)
sp.set_linewidth(2)
ax.set_xticks([])
ax.set_yticks([])
# Confidence Score Bar Chart
ax3 = fig.add_subplot(gs[2, :])
lbls = [r['label'] for r in results]
confs = [r['conf']*100 for r in results]
bcols = [cmap_cls[CLASS_NAMES.index(l)] for l in lbls]
bars = ax3.bar(range(n), confs, color=bcols, edgecolor='black', linewidth=0.5)
ax3.set_xticks(range(n))
ax3.set_xticklabels([f"#{i+1}\n{lbls[i]}" for i in range(n)], fontsize=8, rotation=30, ha='right')
ax3.set_ylabel('Confidence (%)')
ax3.set_ylim(0, 113)
ax3.axhline(40.0, color='red', ls='--', lw=1.2, label='Threshold (40%)')
ax3.legend(fontsize=9)
ax3.grid(axis='y', alpha=0.3)
ax3.set_title('Confidence per detected cell', fontweight='bold')
for bar, v in zip(bars, confs):
ax3.text(bar.get_x() + bar.get_width()/2, v + 1.5, f'{v:.1f}%', ha='center', fontsize=7, fontweight='bold')
# Summary Box at bottom
counts_cnt = Counter(lbls)
summary_str = " ".join([f"{cls}: {count}" for cls, count in sorted(counts_cnt.items())])
fig.text(0.5, 0.005, f"Cell count summary: {summary_str}",
ha='center', fontsize=11, fontweight='bold',
bbox=dict(boxstyle='round,pad=0.4', facecolor='lightyellow', edgecolor='orange'))
plt.suptitle(f'Results — {filename}', fontsize=13, fontweight='bold', y=1.01)
# Save figure to in-memory buffer
buf = io.BytesIO()
plt.savefig(buf, format='jpeg', dpi=120, bbox_inches='tight', facecolor='white')
buf.seek(0)
# Create base64 representation of the combined plot
base64_str = base64.b64encode(buf.read()).decode("utf-8")
plt.close(fig)
# Set prediction outputs
summary_label = ", ".join([f"{count} {cls}" for cls, count in counts_cnt.items()])
predicted_label = f"Detected {len(results)} cells: {summary_label}"
confidence = float(np.mean([res['conf'] for res in results]))
class_probabilities = {WBC_CLASSES[i]: 0.0 for i in range(len(WBC_CLASSES))}
for res in results:
class_probabilities[res['label']] += 1.0
for cls in class_probabilities:
class_probabilities[cls] /= len(results)
# Return the base64 plot directly back to the site
return predicted_label, confidence, class_probabilities, base64_str, time.time() - start_time
else:
# Fallback to single-cell prediction if no cells segmented
is_whole_smear = False
if not is_whole_smear:
transform = get_wbc_transforms()
input_tensor = transform(image).unsqueeze(0)
with torch.no_grad():
outputs = model(input_tensor)
probs = torch.softmax(outputs, dim=1)[0].cpu().numpy()
pred_idx = int(np.argmax(probs))
confidence = float(probs[pred_idx])
predicted_label = WBC_CLASSES[pred_idx]
class_probabilities = {WBC_CLASSES[i]: float(probs[i]) for i in range(len(WBC_CLASSES))}
heatmap_img = generate_wbc_gradcam(model, input_tensor, pred_idx, raw_image_np)
elif module_type == "skin_lesion":
# Load Skin ViT model
processor, model = load_skin_model() |