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import os
import re
import time
import numpy as np
import pandas as pd
import pydicom
import tensorflow as tf
import matplotlib.pyplot as plt
import matplotlib.animation as animation
from utils.layer_util import *
from skimage.measure import label, regionprops
import streamlit as st
import io, shutil, zipfile, time
os.environ["CUDA_DEVICE_ORDER"] = "PCI_BUS_ID"
os.environ["CUDA_VISIBLE_DEVICES"] = "" # Set the GPU to use, if available
if "artifacts" not in st.session_state:
st.session_state.artifacts = {} # {"gif_bytes": ..., "csv_bytes": ...}
if "processed" not in st.session_state:
st.session_state.processed = False
import os
output_root = os.path.join("/tmp", "DICOM_OUTPUTS")
# import neptune.new as neptune
# from neptune.new.integrations.tensorflow_keras import NeptuneCallback
# from neptune.types import File
# Root folder containing all uploaded DICOMs (across patients)
#dicom_path = '/workspaces/PhD/DICOMS'
# Where to write outputs users can download
#output_root = './DICOM_OUTPUTS'
gifs_dir = os.path.join(output_root, 'GIFs')
csv_dir = os.path.join(output_root, 'CSV')
os.makedirs(gifs_dir, exist_ok=True)
os.makedirs(csv_dir, exist_ok=True)
# Path to trained model
model_path = './models_final/SEG459.h5'
# Network input size and class map from training
SIZE_X = 256
SIZE_Y = 256
N_CLASSES = 3 # 0=background, 1=myocardium, 2=blood pool
# For myocardium mass (same constants)
myocardium_density = 1.05 # mg/mm^3 (≈1.05 g/ml)
# --- Island removal toggle & parameters ---
ENABLE_ISLAND_REMOVAL = True
ISLAND_MIN_SLICES = 2 # spans at least this many slices
ISLAND_MIN_AREA = 10 # per-slice minimum area
ISLAND_DISTANCE_THRESH = 40 # max centroid distance (voxels) from dominant component
# =========================================================
# GT-FREE MASK PREPROCESS
# =========================================================
def extract_details_for_sorting(filename):
"""
From your original code: parse filenames like ..._slXX_..._frYY...
Returns: (patient_id, slice_number, frame_number)
"""
base = filename.split('.')[0]
parts = re.split(r'[_-]', base)
slice_idx = next(i for i, p in enumerate(parts) if p.startswith('sl'))
frame_idx = next(i for i, p in enumerate(parts) if p.startswith('fr'))
patient_id = '_'.join(parts[:slice_idx])
slice_number = int(parts[slice_idx].replace('sl', ''))
frame_number = int(parts[frame_idx].replace('fr', ''))
return patient_id, slice_number, frame_number
def normalize_images(images):
"""
Per-image min-max normalization.
Accepts: array (N, H, W, 1) or similar; we use it per-slice.
"""
images = tf.cast(images, tf.float64)
min_val = tf.reduce_min(images, axis=[1, 2], keepdims=True)
max_val = tf.reduce_max(images, axis=[1, 2], keepdims=True)
normalized_images = tf.where(
max_val > min_val,
(images - min_val) / (max_val - min_val),
images
)
return normalized_images
def _tf_resize_pad(img, sx=SIZE_X, sy=SIZE_Y):
return tf.image.resize_with_crop_or_pad(img[:, :, np.newaxis], sx, sy).numpy()[:, :, 0]
def load_process_data_no_gt(dicom_path, SIZE_X, SIZE_Y):
"""
Build per-patient 4D stacks (H, W, S, F) from DICOMs only.
Returns:
- all_frames_test_images: { patient_id: (H, W, S, F) }
- per_patient_used_files: { patient_id: [filepaths in stack order] }
"""
file_names_DICOM = [f for f in os.listdir(dicom_path) if f.lower().endswith('.dcm')]
patients = {}
for f in file_names_DICOM:
try:
pid, sl, fr = extract_details_for_sorting(f)
except Exception:
# If a file doesn't match the pattern, skip it
continue
patients.setdefault(pid, {}).setdefault(fr, []).append((sl, f))
all_frames_test_images = {}
per_patient_used_files = {}
for pid, frames in patients.items():
per_frame_stacks = []
used_files = []
for fr in sorted(frames.keys()):
slices = sorted(frames[fr], key=lambda x: x[0])
imgs = []
for sl, fname in slices:
fp = os.path.join(dicom_path, fname)
ds = pydicom.dcmread(fp)
img = ds.pixel_array.astype(np.float32)
if img.shape[0] != SIZE_X or img.shape[1] != SIZE_Y:
img = _tf_resize_pad(img, SIZE_X, SIZE_Y)
imgs.append(img)
used_files.append(fp)
if imgs:
per_frame_stacks.append(np.stack(imgs, axis=-1)) # (H, W, S)
if per_frame_stacks:
all_frames_test_images[pid] = np.stack(per_frame_stacks, axis=-1) # (H, W, S, F)
per_patient_used_files[pid] = used_files
return all_frames_test_images, per_patient_used_files
# =========================================================
# VOLUME & MASS HELPERS
# =========================================================
def calculate_volume_from_mask(mask, row_mm, col_mm, slice_thickness):
pixel_area = row_mm * col_mm
blood_pool_area = np.sum(mask == 2)
return blood_pool_area * pixel_area * slice_thickness
def calculate_myocardium_mass(mask, row_mm, col_mm, slice_thickness, density):
pixel_area = row_mm * col_mm
myocardium_area = np.sum(mask == 1)
myocardium_volume = myocardium_area * pixel_area * slice_thickness
return myocardium_volume * density
# =========================================================
# DICOM SPACING & THICKNESS
# =========================================================
def read_spacing_thickness_from_files(filepaths):
"""
Return row_mm, col_mm, slice_thickness_mm from DICOM headers.
Fallback for thickness uses ImagePositionPatient z-steps.
"""
row_mm = None
col_mm = None
th = None
z_positions = []
for fp in filepaths:
try:
ds = pydicom.dcmread(fp, stop_before_pixels=True)
except Exception:
continue
if getattr(ds, 'PixelSpacing', None) is not None and row_mm is None and col_mm is None:
row_mm, col_mm = map(float, ds.PixelSpacing) # mm
if getattr(ds, 'SliceThickness', None) is not None and th is None:
th = float(ds.SliceThickness)
ipp = getattr(ds, 'ImagePositionPatient', None)
if ipp is not None and len(ipp) == 3:
z_positions.append(float(ipp[2]))
# Fallback thickness from z-distance
if th is None and len(z_positions) > 1:
z_positions = sorted(z_positions)
diffs = np.diff(z_positions)
diffs = [d for d in diffs if abs(d) > 1e-6]
if diffs:
th = float(np.median(np.abs(diffs)))
# Sensible defaults if missing
if row_mm is None: row_mm = 1.0
if col_mm is None: col_mm = 1.0
if th is None: th = 1.0
return row_mm, col_mm, th
# =========================================================
# MODEL LOAD (ISLAND REMOVAL & LOSS)
# =========================================================
def remove_inconsistent_slices(
segmentation_slices,
min_slices=2,
min_area=10,
distance_threshold=40
):
"""
Keeps components that span >= min_slices and lie within distance_threshold
of the dominant component’s centroid. Class-wise cleaning for labels {1,2}.
"""
H, W, S = segmentation_slices.shape
cleaned_segmentation = np.zeros_like(segmentation_slices, dtype=np.uint8)
for class_label, label_name in [(1, "myocardium"), (2, "blood_pool")]:
binary_mask = (segmentation_slices == class_label).astype(np.uint8)
labels_3d = label(binary_mask, connectivity=1)
regions = [r for r in regionprops(labels_3d) if r.area >= min_area]
if not regions:
continue
dominant_region = max(regions, key=lambda r: len(set(c[2] for c in r.coords)))
dominant_centroid = np.array(dominant_region.centroid)
for region in regions:
slices_present = set(c[2] for c in region.coords)
centroid = np.array(region.centroid)
distance = np.linalg.norm(centroid - dominant_centroid)
if len(slices_present) >= min_slices and distance <= distance_threshold:
for c in region.coords:
cleaned_segmentation[c[0], c[1], c[2]] = class_label
return cleaned_segmentation
def clean_predictions_per_frame(preds_4d,
min_slices=2,
min_area=10,
distance_threshold=40):
"""
Apply remove_inconsistent_slices() to each time frame (H, W, S) of preds_4d (H, W, S, F).
Returns a new array with the same dtype/shape as preds_4d.
"""
H, W, S, F = preds_4d.shape
cleaned = np.empty_like(preds_4d)
for f in range(F):
cleaned[..., f] = remove_inconsistent_slices(
preds_4d[..., f],
min_slices=min_slices,
min_area=min_area,
distance_threshold=distance_threshold
)
return cleaned
def dice(y_true, y_pred, smooth=1e-6):
y_true_f = tf.reshape(tf.cast(y_true, tf.float32), [-1])
y_pred_f = tf.reshape(tf.clip_by_value(y_pred, 0.0, 1.0), [-1])
intersection = tf.reduce_sum(y_true_f * y_pred_f)
union = tf.reduce_sum(y_true_f) + tf.reduce_sum(y_pred_f)
return (2. * intersection + smooth) / (union + smooth)
def dice_coef_class(class_index, name=None, smooth=1e-6):
def wrapped_dice(y_true, y_pred):
y_true_c = tf.cast(y_true[..., class_index], tf.float32)
y_pred_c = tf.clip_by_value(y_pred[..., class_index], 0.0, 1.0)
y_true_f = tf.reshape(y_true_c, [-1])
y_pred_f = tf.reshape(y_pred_c, [-1])
intersection = tf.reduce_sum(y_true_f * y_pred_f)
union = tf.reduce_sum(y_true_f) + tf.reduce_sum(y_pred_f)
return (2. * intersection + smooth) / (union + smooth)
return tf.keras.metrics.MeanMetricWrapper(wrapped_dice, name=name or f'dice_class_{class_index}')
def dice_coef_no_bkg(y_true, y_pred, smooth=1e-6):
y_true = tf.cast(y_true, tf.float32)
y_pred = tf.cast(y_pred, tf.float32)
y_true_fg = y_true[..., 1:]
y_pred_fg = y_pred[..., 1:]
y_true_f = tf.reshape(y_true_fg, [-1, tf.shape(y_true_fg)[-1]])
y_pred_f = tf.reshape(y_pred_fg, [-1, tf.shape(y_pred_fg)[-1]])
intersection = tf.reduce_sum(y_true_f * y_pred_f, axis=0)
denominator = tf.reduce_sum(y_true_f + y_pred_f, axis=0)
dice_vals = (2. * intersection + smooth) / (denominator + smooth)
return tf.reduce_mean(dice_vals)
def focal_tversky_loss(y_true, y_pred, alpha=0.5, beta=0.5, gamma=1.0, smooth=1e-6):
y_true = tf.cast(y_true, tf.float32)
y_pred = tf.clip_by_value(y_pred, smooth, 1.0 - smooth)
num_classes = 3
loss = 0.0
for c in range(num_classes):
y_true_c = y_true[..., c]
y_pred_c = y_pred[..., c]
true_pos = tf.reduce_sum(y_true_c * y_pred_c)
false_neg = tf.reduce_sum(y_true_c * (1 - y_pred_c))
false_pos = tf.reduce_sum((1 - y_true_c) * y_pred_c)
tversky_index = (true_pos + smooth) / (true_pos + alpha * false_neg + beta * false_pos + smooth)
loss += tf.pow((1 - tversky_index), gamma)
return loss / tf.cast(num_classes, tf.float32)
CUSTOM_OBJECTS = {
'focal_tversky_loss': focal_tversky_loss,
'dice_coef_no_bkg': dice_coef_no_bkg,
'ResizeAndConcatenate': ResizeAndConcatenate,
'dice_myo': dice_coef_class(1, name='dice_myo'),
'dice_blood': dice_coef_class(2, name='dice_blood'),
'dice': dice
}
# =========================================================
# PREDICTION
# =========================================================
def predict_patient_images(model, images_4d):
"""
Mirrors your original prediction shape logic:
- For each frame, feed (S,H,W,1)
- Use last deep-supervision head if list
- Argmax to labels {0,1,2}, then reshape back to (H,W,S,F)
"""
H, W, S, F = images_4d.shape
preds = np.zeros((H, W, S, F), dtype=np.uint8)
for f in range(F):
frame = images_4d[..., f] # (H,W,S)
batch = np.moveaxis(frame, -1, 0)[..., np.newaxis].astype(np.float32) # (S,H,W,1)
batch = normalize_images(batch).numpy()
out = model.predict(batch, verbose=0)
if isinstance(out, list):
out = out[-1]
lab = np.argmax(out, axis=-1).astype(np.uint8) # (S,H,W)
lab = np.moveaxis(lab, 0, -1) # (H,W,S)
preds[..., f] = lab
return preds
# =========================================================
# ED/ES PICKER FROM PRED
# =========================================================
def pick_ed_es_from_predictions(
preds_4d,
row_mm,
col_mm,
slice_thickness_mm,
prefer_frame0: bool = True,
rel_tolerance: float = 0.05, # keep frame 0 as ED if within 5% of argmax
abs_tolerance_uL: float = 0.0, # or within this absolute tolerance (µL); 0 = ignore
min_temporal_separation: int = 0 # ensure ES is at least this many frames away from ED
):
"""
ED/ES selection:
- Compute LV blood-pool volume per frame from predicted labels (class==2).
- If prefer_frame0=True, default ED=0 but validate vs argmax(volume):
* If volume(frame0) within tolerance of max(volume), keep ED=0.
* Else, ED=argmax(volume).
- ES = argmin(volume), with safeguards so ES != ED and (optionally) not too
close in time to ED.
Returns
-------
ed_idx : int
es_idx : int
frame_vols : list[float] (per-frame volumes in µL)
"""
import numpy as np
H, W, S, F = preds_4d.shape
frame_vols = []
for f in range(F):
v = calculate_volume_from_mask(preds_4d[..., f], row_mm, col_mm, slice_thickness_mm)
frame_vols.append(float(v))
# Physiologic candidates
ed_argmax = int(np.argmax(frame_vols))
es_argmin = int(np.argmin(frame_vols))
# --- ED selection---
if prefer_frame0 and F > 0:
v0 = frame_vols[0]
vmax = frame_vols[ed_argmax]
# If max is non-positive, just use frame 0
if vmax <= 0:
ed_idx = 0
ed_source = "frame0_fallback_vmax<=0"
else:
# Keep frame 0 if it's close enough to the argmax
close_by_rel = abs(vmax - v0) <= (rel_tolerance * vmax)
close_by_abs = (abs_tolerance_uL > 0.0) and (abs(vmax - v0) <= abs_tolerance_uL)
if close_by_rel or close_by_abs:
ed_idx = 0
ed_source = "frame0_within_tolerance"
else:
ed_idx = ed_argmax
ed_source = "argmax"
else:
ed_idx = ed_argmax
ed_source = "argmax"
# --- ES selection ---
# Start from pure argmin
es_idx = es_argmin
# Ensure ES != ED and optionally far enough from ED in time
# --- ES selection (with safeguards) ---
# Start from pure argmin
es_idx = es_argmin
if es_idx == ed_idx or (min_temporal_separation > 0 and abs(es_idx - ed_idx) < min_temporal_separation):
order = np.argsort(frame_vols)
chosen = None
for idx in order:
if idx == ed_idx:
continue
if min_temporal_separation > 0 and abs(int(idx) - ed_idx) < min_temporal_separation:
continue
chosen = int(idx)
break
es_idx = chosen if chosen is not None else int(order[0] if int(order[0]) != ed_idx else (order[1] if len(order) > 1 else ed_idx))
return int(ed_idx), int(es_idx), frame_vols
# =========================================================
# GIF MAKER (NO GT)
# =========================================================
def gif_animation_for_patient_pred_only(images_4d, preds_4d, patient_id, ed_idx, es_idx, output_dir):
import os
import matplotlib.pyplot as plt
from matplotlib import animation
os.makedirs(output_dir, exist_ok=True)
def overlay(ax, img, pred):
ax.imshow(img, cmap='gray')
ax.imshow((pred == 1), alpha=(pred == 1) * 0.5, cmap='Blues') # myocardium
ax.imshow((pred == 2), alpha=(pred == 2) * 0.5, cmap='jet') # blood pool
ax.axis('off')
H, W, S, F = images_4d.shape
fig, axarr = plt.subplots(1, 2, figsize=(8, 4))
plt.tight_layout(rect=[0, 0, 1, 0.92]) # leave space at top for patient ID
def update(slice_idx):
axarr[0].clear()
axarr[1].clear()
overlay(axarr[0], images_4d[:, :, slice_idx, ed_idx], preds_4d[:, :, slice_idx, ed_idx])
axarr[0].set_title(f'ED (frame {ed_idx}) | Slice {slice_idx}') # extra spaces before/after '|'
overlay(axarr[1], images_4d[:, :, slice_idx, es_idx], preds_4d[:, :, slice_idx, es_idx])
axarr[1].set_title(f'ES (frame {es_idx}) | Slice {slice_idx}')
# Large, centered patient ID at the top
fig.suptitle(f'Patient ID: {patient_id}', fontsize=14, y=0.98)
anim = animation.FuncAnimation(fig, update, frames=S, interval=700)
out_path = os.path.join(output_dir, f"{patient_id}_pred.gif")
anim.save(out_path, writer='pillow')
plt.close(fig)
return out_path
def _is_dicom_file(path):
if not os.path.isfile(path):
return False
# Fast + robust: try pydicom first; fall back to DICM preamble
try:
import pydicom
try:
pydicom.dcmread(path, stop_before_pixels=True, force=True)
return True
except Exception:
return False
except ImportError:
# fallback check: 128-byte preamble + 'DICM' marker (not guaranteed for all files)
try:
with open(path, "rb") as f:
f.seek(128)
return f.read(4) == b"DICM"
except Exception:
return False
def _count_dicoms_here(dir_path, max_check=500):
"""Count DICOM files directly inside dir_path (non-recursive), up to max_check files."""
count = 0
for name in os.listdir(dir_path):
fp = os.path.join(dir_path, name)
if os.path.isfile(fp) and _is_dicom_file(fp):
count += 1
if count >= max_check:
break
return count
def find_dicom_series_dirs(root, min_files=3):
"""
Walk the tree and collect directories that contain >= min_files DICOMs directly inside them.
Prunes descent once a directory is identified as a series dir.
"""
series = []
for curr, dirnames, filenames in os.walk(root, topdown=True):
# Ignore hidden/OS cruft
dirnames[:] = [d for d in dirnames if not d.startswith('.') and d != '__MACOSX']
dicom_count = _count_dicoms_here(curr)
if dicom_count >= min_files:
series.append((curr, dicom_count))
dirnames[:] = [] # don't descend further under a series dir
# sort by most DICOM files first
series.sort(key=lambda t: t[1], reverse=True)
return series
def clear_dir(path):
"""Remove all contents of a directory, but keep the directory itself."""
if os.path.exists(path):
for fname in os.listdir(path):
fpath = os.path.join(path, fname)
if os.path.isfile(fpath) or os.path.islink(fpath):
os.remove(fpath)
elif os.path.isdir(fpath):
shutil.rmtree(fpath)
else:
os.makedirs(path, exist_ok=True)
def process_zip_and_make_artifacts(uploaded_zip):
# ... your existing extraction + processing ...
# e.g., write GIF to a BytesIO and CSV to bytes
gif_buf = BytesIO()
# anim.save(gif_buf, writer="pillow", format="gif"); gif_buf.seek(0)
# For demo, pretend we have bytes:
# gif_buf.write(b"..."); gif_buf.seek(0)
csv_bytes = b"col1,col2\n1,2\n3,4\n"
return gif_buf.getvalue(), csv_bytes
# =========================================================
# MAIN
# =========================================================
def main():
import os
# os.makedirs(output_root, exist_ok=True)
# os.makedirs(gifs_dir, exist_ok=True)
# os.makedirs(csv_dir, exist_ok=True)
#os.makedirs("./DICOM_OUTPUTS", exist_ok=True)
# put this near the top of your app.py
clear_dir("/tmp/out_dicoms")
clear_dir("/tmp/DICOM_OUTPUTS/CSV")
clear_dir("/tmp/DICOM_OUTPUTS/GIFs")
st.header("Data Upload")
uploaded_zip = st.file_uploader("Upload ZIP file of MRI folders", type="zip")
def extract_zip(zip_path, extract_to):
import zipfile, os
os.makedirs(extract_to, exist_ok=True)
with zipfile.ZipFile(zip_path, 'r') as zip_ref:
valid_files = [
f for f in zip_ref.namelist()
if "__MACOSX" not in f and not os.path.basename(f).startswith("._")
]
zip_ref.extractall(extract_to, members=valid_files)
if uploaded_zip is not None and st.button("Process Data"):
with st.spinner("Processing ZIP..."):
extract_root = '/tmp/out_dicoms'
os.makedirs(extract_root, exist_ok=True)
zip_path = os.path.join(extract_root, "upload.zip")
with open(zip_path, "wb") as f:
f.write(uploaded_zip.read())
extract_zip(zip_path, extract_root)
# 1) Automatically find the best DICOM series directory
series = find_dicom_series_dirs(extract_root, min_files=3)
if not series:
st.error("No DICOM series found in the uploaded ZIP.")
st.stop()
# Choose the directory with the most DICOM files
dicom_dir, dicom_count = series[0]
st.success(f"Detected DICOM folder: {dicom_dir} (≈{dicom_count} files)")
all_frames_test_images, per_patient_used_files = load_process_data_no_gt(
dicom_dir, SIZE_X, SIZE_Y
)
print(f"Total patients found: {len(all_frames_test_images)}")
# 2) Load model
model = tf.keras.models.load_model(model_path, custom_objects=CUSTOM_OBJECTS)
print('Loaded model successfully')
print(f"Model input shape: {model.input_shape}")
print(f"Model output shape: {model.output_shape}")
# 3) For each patient: predict -> (optional clean) -> ED/ES -> GIF -> CSV row
rows = []
for pid, images_4d in sorted(all_frames_test_images.items()):
print(f"\nProcessing patient: {pid} | 4D shape: {images_4d.shape}")
# Spacing & thickness from headers of files used for this stack
used_files = per_patient_used_files.get(pid, [])
row_mm, col_mm, slice_thickness_mm = read_spacing_thickness_from_files(used_files)
print(f"Spacing/thickness: row={row_mm:.4f} mm, col={col_mm:.4f} mm, th={slice_thickness_mm:.4f} mm")
# Predict labels
preds_4d = predict_patient_images(model, images_4d)
# ✅ Optionally clean per-frame predictions to remove islands
if ENABLE_ISLAND_REMOVAL:
preds_4d = clean_predictions_per_frame(
preds_4d,
min_slices=ISLAND_MIN_SLICES,
min_area=ISLAND_MIN_AREA,
distance_threshold=ISLAND_DISTANCE_THRESH
)
# Choose ED/ES from predicted blood-pool volumes
ed_idx, es_idx, frame_vols = pick_ed_es_from_predictions(preds_4d, row_mm, col_mm, slice_thickness_mm)
print(f"Selected ED frame: {ed_idx}, ES frame: {es_idx}")
# Cardiac metrics from predictions only (mm^3 == µL)
EDV_uL = calculate_volume_from_mask(preds_4d[..., ed_idx], row_mm, col_mm, slice_thickness_mm)
ESV_uL = calculate_volume_from_mask(preds_4d[..., es_idx], row_mm, col_mm, slice_thickness_mm)
SV_uL = EDV_uL - ESV_uL
EF_pct = (SV_uL / EDV_uL * 100.0) if EDV_uL > 0 else 0.0
myo_mass_ED_mg = calculate_myocardium_mass(preds_4d[..., ed_idx], row_mm, col_mm, slice_thickness_mm, myocardium_density)
myo_mass_ES_mg = calculate_myocardium_mass(preds_4d[..., es_idx], row_mm, col_mm, slice_thickness_mm, myocardium_density)
# GIF (prediction-only overlays)
gif_path = gif_animation_for_patient_pred_only(images_4d, preds_4d, pid, ed_idx, es_idx, gifs_dir)
st.image(gif_path, caption="Generated GIF", use_container_width=True)
print(f"GIF saved: {gif_path}")
# CSV row (predictions only)
rows.append({
'Patient_ID': pid,
'EDV_uL': EDV_uL,
'ESV_uL': ESV_uL,
'SV_uL' : SV_uL,
'EF_%' : EF_pct,
'MyocardiumMass_ED_mg': myo_mass_ED_mg,
'MyocardiumMass_ES_mg': myo_mass_ES_mg,
'ED_frame_index': ed_idx,
'ES_frame_index': es_idx,
'PixelSpacing_row_mm': row_mm,
'PixelSpacing_col_mm': col_mm,
'SliceThickness_mm': slice_thickness_mm
})
# 4) Save CSV/Excel
df = pd.DataFrame(rows)
os.makedirs(csv_dir, exist_ok=True)
csv_path = os.path.join(csv_dir, 'Cardiac_Volumes_And_Mass_fromPredictions.csv')
xlsx_path = os.path.join(csv_dir, 'Cardiac_Volumes_And_Mass_fromPredictions.xlsx')
df.to_csv(csv_path, index=False)
df.to_excel(xlsx_path, index=False)
print(f"\nCSV written: {csv_path}")
print(f"Excel written: {xlsx_path}")
st.session_state.processed = True
if st.session_state.processed == True:
with open(gif_path, "rb") as f:
st.download_button(
label="📥 Download GIF",
data=f,
file_name="mask.gif",
mime="image/gif"
)
with open(csv_path, "rb") as f:
st.download_button(
label="Download CSV",
data=f,
file_name="/Cardiac_Volumes_And_Mass_fromPredictions.csv",
mime="text/csv"
)
if __name__ == '__main__':
main()