Image-Text-to-Text
PEFT
Safetensors
English
Turkish
early_diagnosis
reasoning
diagnosis
health
healthcare
alzheimer
athropy
dementia
biomarkers
biology
academic
lora
mri
Instructions to use Neurazum/VLbai-2.6AD with libraries, inference providers, notebooks, and local apps. Follow these links to get started.
- Libraries
- PEFT
How to use Neurazum/VLbai-2.6AD with PEFT:
Task type is invalid.
- Notebooks
- Google Colab
- Kaggle
File size: 9,550 Bytes
1013007 | 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 | """
Feature extraction — step 1 of the LLM integration
==================================================
Runs Vbai-2.6AD FROZEN and writes everything the LLM will need into a single
file. Because the encoder is frozen this is a one-off: every later projector or
LoRA experiment reads this cache and never touches the 3D CNN again.
Stored per visit:
fused_features (512) the representation behind the 0.895 accuracy; the
projector's main input
mri_features (512) imaging branch
tab_features (256) biomarker branch
class_probs (3) CN/MCI/AD — the LLM's ANCHOR, also written as text
will_progress (1) MCI -> AD risk score
label, ptid, split, nifti_path
bio_values (13) + bio_mask (13) raw values for the text template
(mask = 0 means "not measured" and must be
stated, never silently skipped)
NOTE — no spatial tokens. token_probe.py showed the post-ASPP 3x3x3 grid is
degenerate (attention entropy at 98.9% of maximum), i.e. the 27 tokens carry
nothing beyond the pooled vector. The pooled representation itself is sound
(fresh probe macro-F1 0.464, MCI F1 0.474).
Run:
python extract_features.py --tbm --ckpt Vbai-2.6AD.pt --out features.pt
"""
from __future__ import annotations
import argparse
import os
import sys
# --- The modality must be chosen BEFORE config is imported: config decides at
# import time which visit manifest to read.
_ap = argparse.ArgumentParser(add_help=False)
_ap.add_argument("--tbm", action="store_true")
_ap.add_argument("--t1", action="store_true")
_known, _ = _ap.parse_known_args()
if _known.tbm == _known.t1:
sys.exit("ERROR: pass exactly one of --tbm / --t1 "
"(match whichever modality the checkpoint was trained on).")
os.environ["VBAI_USE_TBM"] = "1" if _known.tbm else "0"
MODALITY = "TBM" if _known.tbm else "raw T1"
def _bootstrap_model_path() -> str:
"""
Locate config.py / model.py / dataset.py.
YOU MUST SET YOUR OWN PATH if they do not sit next to this script: point
VBAI_MODEL_DIR at the directory holding them.
"""
env = os.environ.get("VBAI_MODEL_DIR")
cands = ([env] if env else []) + [
os.path.dirname(os.path.abspath(__file__)),
os.path.join(os.path.dirname(os.path.abspath(__file__)), "Vbai-2.6AD"),
]
for c in cands:
if c and os.path.isfile(os.path.join(c, "config.py")):
if c not in sys.path:
sys.path.insert(0, c)
return c
raise ImportError(
f"Could not locate the model modules (config.py). Tried: {cands}\n"
"YOU MUST SET YOUR OWN PATH: point VBAI_MODEL_DIR at the directory "
"holding config.py / model.py / dataset.py."
)
MODEL_DIR = _bootstrap_model_path()
import numpy as np
import torch
from tqdm import tqdm
import config as C
from model import Vbai26ADModel
from dataset import (PairedVisitDataset, TabularNormalizer, collate_pad,
subject_split, load_paired)
def remap_paths(df):
"""
Re-root the volume paths stored in the manifest.
A manifest built on one machine carries that machine's absolute paths. Rather
than forcing a rebuild, the tail of each path is re-attached to the roots
configured here.
"""
def _fix(p):
p0 = str(p)
if os.path.exists(p0):
return p0
q = p0.replace("\\", "/")
i = q.find("/Datasets/")
if i >= 0:
cand = os.path.join(C.DATASET_ROOT, q[i + len("/Datasets/"):])
if os.path.exists(cand):
return cand
# Volume root: the manifest tail may or may not include the top folder,
# so both spellings are tried.
j = q.find("/volumes/")
if j >= 0:
rest = q[j + len("/volumes/"):]
for cand in (os.path.join(C.TBM_ROOT, rest),
os.path.join(C.TBM_ROOT, "volumes", rest)):
if os.path.exists(cand):
return cand
return p0
df = df.copy()
df["nifti_path"] = df["nifti_path"].map(_fix)
ok = int(sum(os.path.exists(str(p)) for p in df["nifti_path"]))
print(f"[path] reachable images ({MODALITY}): {ok}/{len(df)}")
if ok == 0:
raise FileNotFoundError(
f"No image is reachable.\n DATASET_ROOT={C.DATASET_ROOT}\n"
f" VOLUME_ROOT={C.TBM_ROOT}\n"
"YOU MUST SET YOUR OWN PATHS: see VBAI_DATASET_ROOT / "
"VBAI_VOLUME_ROOT in config.py."
)
return df[df["nifti_path"].map(lambda p: os.path.exists(str(p)))].reset_index(drop=True)
def main():
ap = argparse.ArgumentParser()
ap.add_argument("--ckpt", default="Vbai-2.6AD.pt", help="Vbai-2.6AD checkpoint")
ap.add_argument("--out", required=True, help="output .pt path")
ap.add_argument("--tbm", action="store_true")
ap.add_argument("--t1", action="store_true")
ap.add_argument("--batch-size", type=int, default=4)
ap.add_argument("--workers", type=int, default=2)
args = ap.parse_args()
dev = torch.device("cuda" if torch.cuda.is_available() else "cpu")
print(f"[device] {dev} | [modality] {MODALITY} | "
f"[manifest] {os.path.basename(C.PAIRED_PARQUET)}")
sd = torch.load(args.ckpt, map_location=dev, weights_only=False)
mcfg = C.ModelConfig()
for k, v in sd.get("model_cfg", {}).items():
if hasattr(mcfg, k):
setattr(mcfg, k, v)
model = Vbai26ADModel(mcfg).to(dev)
res = model.load_state_dict(sd["model"], strict=False)
# Loading with strict=False and ignoring the result is how a silently wrong
# checkpoint slips through, so any key mismatch is fatal here.
if res.missing_keys or res.unexpected_keys:
raise RuntimeError(
f"Checkpoint does not match the architecture: "
f"{len(res.missing_keys)} missing / {len(res.unexpected_keys)} "
f"unexpected keys. Wrong model file?")
model.eval()
for p in model.parameters():
p.requires_grad_(False)
print(f"[ckpt] {len(sd['model'])} keys matched | {sd.get('extra', {}).get('metrics')}")
norm = TabularNormalizer()
norm.load_state_dict(sd["norm"])
feat_names = sd.get("feature_names", C.FEATURE_NAMES)
df = remap_paths(load_paired())
train_ids, val_ids, test_ids = subject_split(df)
split_of = {}
for s, ids in (("train", train_ids), ("val", val_ids), ("test", test_ids)):
for i in ids:
split_of[i] = s
df["split"] = df["ptid"].map(split_of)
ds = PairedVisitDataset(df, norm, mode="multi", augment=False, mcfg=mcfg)
dl = torch.utils.data.DataLoader(ds, batch_size=args.batch_size, shuffle=False,
collate_fn=collate_pad, num_workers=args.workers)
acc = {k: [] for k in ["fused_features", "mri_features", "tab_features",
"class_probs", "will_progress", "label"]}
n_seen = 0
with torch.no_grad():
for b in tqdm(dl, desc="extracting features"):
if "mri" not in b or "tab" not in b:
raise RuntimeError("Batch is missing mri or tab — "
"modality dropout must be off here.")
out = model(mri=b["mri"].to(dev), tab=b["tab"].to(dev))
acc["fused_features"].append(out["fused_features"].cpu())
acc["mri_features"].append(out["mri_features"].cpu())
acc["tab_features"].append(out["tab_features"].cpu())
acc["class_probs"].append(torch.softmax(out["fused_logits"], -1).cpu())
acc["will_progress"].append(out["progression"]["will_progress"].cpu())
acc["label"].append(b["label"])
n_seen += b["label"].size(0)
store = {k: torch.cat(v).float() for k, v in acc.items()}
store["label"] = store["label"].long()
# DataLoader order matches df order (shuffle=False), so metadata lines up.
assert n_seen == len(df), f"sample count mismatch: {n_seen} vs {len(df)}"
store["ptid"] = df["ptid"].tolist()
store["split"] = df["split"].tolist()
store["nifti_path"] = df["nifti_path"].tolist()
# RAW (un-normalised) biomarker values plus their mask, for the text template.
vals = np.stack([np.where(np.isnan(df[f].values.astype(np.float32)), 0.0,
df[f].values.astype(np.float32)) for f in feat_names], axis=1)
mask = np.stack([df[f"feat_mask_{f}"].values.astype(np.float32) for f in feat_names], axis=1)
store["bio_values"] = torch.from_numpy(vals)
store["bio_mask"] = torch.from_numpy(mask)
store["feature_names"] = list(feat_names)
store["class_names"] = sd.get("class_names", C.CLASS_NAMES)
store["modality"] = MODALITY
store["ckpt"] = os.path.abspath(args.ckpt)
os.makedirs(os.path.dirname(os.path.abspath(args.out)) or ".", exist_ok=True)
torch.save(store, args.out)
from collections import Counter
print(f"\n[saved] {args.out}")
print(f" visits : {len(df)} | patients: {df['ptid'].nunique()}")
print(f" split : {Counter(store['split'])}")
print(f" fused_features: {tuple(store['fused_features'].shape)}")
print(f" bio_values : {tuple(store['bio_values'].shape)} (with mask)")
print(" measured rate : " + ", ".join(
f"{n}={store['bio_mask'][:, i].mean():.2f}" for i, n in enumerate(feat_names)))
print("\nNext: train the projector on this cache (the LLM stays frozen).")
if __name__ == "__main__":
main()
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