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141bacd | 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 | """zero-shot inference over every held-out target x (pca, marker) checkpoint."""
from pathlib import Path
import warnings, json, sys, pickle, argparse, numpy as np, pandas as pd, anndata as ad, scanpy as sc, scipy.sparse as sp, torch, torch.nn.functional as F
warnings.filterwarnings("ignore"); sc.settings.verbosity = 0
import os as _os
from pathlib import Path as _Path
PANDA_ROOT = _Path(_os.environ.get("PANDA_ROOT", str(_Path(__file__).resolve().parents[2])))
sys.path.insert(0, str(PANDA_ROOT))
from panda import PANDAEncoder
from sklearn.metrics import accuracy_score, f1_score, classification_report
ROOT = Path(str(PANDA_ROOT))
DEVICE = torch.device("cuda" if torch.cuda.is_available() else "cpu")
def infer(a, system, variant):
ck = torch.load(ROOT / f"checkpoints/{system}/{variant}/panda_final.pt",
map_location=DEVICE, weights_only=False)
classes = ck["classes"]; marker_genes = ck.get("marker_genes", [])
stats = np.load(ROOT / f"data/corpus/{system}/harmonized/corpus_stats.npz", allow_pickle=True)
pca = pickle.load(open(ROOT / f"data/corpus/{system}/harmonized/pca_basis.pkl", "rb"))
hvgs = [str(g) for g in stats["shared_hvgs"]]
hvg2i = {g: i for i, g in enumerate(hvgs)}
# human->mouse symbol case-fold (same heuristic as zero_shot.py): corpora + markers.yaml
# use mouse Title-case symbols; human targets (e.g. veres) ship ALL-CAPS HGNC symbols.
# Without this the HVG intersection collapses to ~0 and predictions are meaningless.
vn = a.var_names.astype(str)
n_upper = sum(1 for g in vn[:1000] if g.isupper() and len(g) > 1)
if n_upper > 500:
a = a.copy()
a.var_names = [g.capitalize() for g in vn]
a.var_names_make_unique()
print(f"[infer] case-folded {n_upper}/1000 uppercase symbols human->mouse", flush=True)
common = [g for g in a.var_names.astype(str) if g in hvg2i]
if len(common) < 0.2 * len(hvgs):
print(f"[infer] WARNING: only {len(common)}/{len(hvgs)} corpus HVGs present in target; "
f"predictions will be unreliable", flush=True)
a_c = a[:, common].copy()
sc.pp.normalize_total(a_c, target_sum=1e4); sc.pp.log1p(a_c)
X = a_c.X.toarray().astype(np.float32) if sp.issparse(a_c.X) else a_c.X.astype(np.float32)
Xf = np.zeros((a.n_obs, len(hvgs)), dtype=np.float32)
Xf[:, np.array([hvg2i[g] for g in common])] = X
Xz = np.clip((Xf - stats["mean"].astype(np.float32)) / stats["std"].astype(np.float32), -10, 10)
Xpca = pca.transform(Xz).astype(np.float32)
Xmark = None
if variant == "marker":
mv = np.zeros((a.n_obs, len(marker_genes)), dtype=np.float32)
for j, g in enumerate(marker_genes):
if g in a.var_names:
col = a[:, g].X
if sp.issparse(col): col = col.toarray()
mv[:, j] = col.flatten().astype(np.float32)
# prefer the training-corpus marker stats stored in the checkpoint; refitting on the
# target puts the marker channel on a target-dependent scale the model never saw
if ck.get("marker_mu") is not None and ck.get("marker_sig") is not None:
mmu = np.asarray(ck["marker_mu"], dtype=np.float32)
msig = np.asarray(ck["marker_sig"], dtype=np.float32)
else:
print("[infer] WARNING: checkpoint lacks marker_mu/sig; z-scoring markers on the "
"target itself (legacy behaviour, target-dependent scale)", flush=True)
mmu = mv.mean(axis=0, keepdims=True); msig = mv.std(axis=0, keepdims=True) + 1e-6
Xmark = np.clip((mv - mmu) / msig, -5, 5).astype(np.float32)
model = PANDAEncoder(variant=variant, n_pca=50,
n_markers=len(marker_genes) if variant == "marker" else 0,
n_classes=len(classes), n_sub=3,
n_datasets=len(ck["datasets"])).to(DEVICE).eval()
model.load_state_dict(ck["model"])
preds, probs, coss = [], [], []
with torch.no_grad():
for i in range(0, a.n_obs, 4096):
xb = torch.from_numpy(Xpca[i:i+4096]).to(DEVICE)
xmb = torch.from_numpy(Xmark[i:i+4096]).to(DEVICE) if Xmark is not None else None
aux = torch.zeros(len(xb), 2, device=DEVICE)
out = model(xb, aux, x_markers=xmb, lam_dann=0.0)
mc = model.max_sub_cos(out["z"])
preds.append(mc.argmax(dim=1).cpu().numpy())
coss.append(mc.max(dim=1).values.cpu().numpy())
probs.append(F.softmax(mc / 0.07, dim=1).cpu().numpy())
return (np.array([classes[i] for i in np.concatenate(preds)]),
np.concatenate(probs), np.concatenate(coss), classes)
TARGETS = {
"pan_skin": [
("dingwall", ROOT / "data/raw/GSE220977_combined.h5ad", None),
# WARNING: all 4,683 sulic cells (incl. this 4,183-cell "test" slice) are inside
# data/corpus/pan_skin/harmonized/corpus.h5ad (verified by barcode overlap 2026-08-19).
# Scoring the standard corpus checkpoint here is a TRAIN-SET evaluation, not held-out.
# Use scripts/pan_skin/92_retrain_with_sulic_anchor.py (500-cell anchor, rest held out)
# for an honest Sulic number.
("sulic", ROOT / "data/corpus/pan_skin/held_out_labeled/sulic_GSE212673_test.h5ad", "canonical_label"),
("belote", ROOT / "data/corpus/pan_skin/held_out_labeled/belote_GSE151091_test.h5ad", "canonical_label"),
],
"hematopoiesis": [
("nestorowa", ROOT / "data/corpus/hematopoiesis/held_out_labeled/nestorowa_GSE81682_test.h5ad", "cell_type"),
("dahlin", None, None), # loaded per-file via loader (61k cells across 8 samples)
],
"pancreas": [
("baron", ROOT / "data/corpus/pancreas/held_out_labeled/baron_GSE84133_mouse_test.h5ad", "canonical_label"),
("veres", ROOT / "data/corpus/pancreas/held_out_labeled/veres_GSE114412_test.h5ad", "canonical_label"),
],
}
def load_dahlin():
"""dahlin 61k held-out unlabeled hsc target, 8 sample files."""
D = ROOT / "data/corpus/hematopoiesis/held_out_unlabeled/dahlin_extract"
GT = {"SIGAB1":"WT","SIGAC1":"WT","SIGAD1":"WT","SIGAF1":"WT","SIGAG1":"WT",
"SIGAH1":"WT","SIGAG8":"Kit_W41","SIGAH8":"Kit_W41"}
parts = []
for f in sorted(D.glob("*.txt.gz")):
sample = f.name.split("_")[1].split(".")[0]
df = pd.read_csv(f, sep="\t", compression="gzip", index_col=0)
X = sp.csr_matrix(df.values.T.astype(np.float32))
obs = pd.DataFrame(index=[f"{sample}_{bc}" for bc in df.columns.astype(str)])
obs["sample"] = sample; obs["genotype"] = GT.get(sample, "unknown")
var = pd.DataFrame(index=df.index.astype(str))
parts.append(ad.AnnData(X=X, obs=obs, var=var))
a = ad.concat(parts, join="outer")
import mygene
mg = mygene.MyGeneInfo()
res = mg.querymany(a.var_names.astype(str).tolist(), scopes="ensembl.gene",
fields="symbol", species="mouse", verbose=False)
id2sym = {r["query"]: r["symbol"] for r in res if "symbol" in r}
syms = pd.Series(a.var_names.astype(str)).map(id2sym).values
keep = pd.notna(syms)
a = a[:, keep].copy(); a.var_names = syms[keep]; a.var_names_make_unique()
return a
def process(system, variant):
print(f"\n===== {system} / {variant} =====", flush=True)
for tgt_name, tgt_path, tgt_label in TARGETS[system]:
print(f"\n[{tgt_name}] loading", flush=True)
if tgt_name == "dahlin":
a = load_dahlin()
else:
a = ad.read_h5ad(tgt_path)
print(f"[{tgt_name}] {a.shape}", flush=True)
pred, probs, max_cos, classes = infer(a, system, variant)
out_dir = ROOT / f"discovery/{system}/{variant}"
out_dir.mkdir(parents=True, exist_ok=True)
# max_cos is the genuine prototype cosine; max_prob is softmax(max_cos/0.07).
# (earlier revisions wrote the softmax value under the name max_cos)
pd.DataFrame({
"cell_id": a.obs_names,
"pred_label": pred,
"max_cos": max_cos,
"max_prob": probs.max(axis=1),
}).to_csv(out_dir / f"{tgt_name}_predictions.csv", index=False)
summary = {
"system": system, "variant": variant, "target": tgt_name,
"n_cells": int(a.n_obs), "n_classes_model": len(classes),
"predicted_class_dist": pd.Series(pred).value_counts().head(30).to_dict(),
"max_cos_p50": float(np.median(max_cos)),
"max_cos_p05": float(np.quantile(max_cos, 0.05)),
"max_prob_p50": float(np.median(probs.max(axis=1))),
"max_prob_p05": float(np.quantile(probs.max(axis=1), 0.05)),
}
if tgt_label and tgt_label in a.obs.columns:
y_true = a.obs[tgt_label].astype(str).values
mask = np.isin(y_true, classes)
if mask.sum() > 0:
acc = accuracy_score(y_true[mask], pred[mask])
f1 = f1_score(y_true[mask], pred[mask], average="macro", zero_division=0)
rep = classification_report(y_true[mask], pred[mask],
zero_division=0, output_dict=True)
summary["labeled_eval"] = {
"n_eval": int(mask.sum()), "acc": float(acc),
"n_excluded_off_vocab": int((~mask).sum()),
"excluded_label_dist": pd.Series(y_true[~mask]).value_counts().head(20).to_dict(),
"macro_f1": float(f1), "per_class_report": rep,
}
print(f"[{tgt_name}] acc={acc:.4f} F1={f1:.4f} on {mask.sum()} labeled cells", flush=True)
(out_dir / f"{tgt_name}_summary.json").write_text(json.dumps(summary, indent=2, default=str))
print(f"[{tgt_name}] wrote {out_dir}/{tgt_name}_predictions.csv + summary.json", flush=True)
def main():
ap = argparse.ArgumentParser()
ap.add_argument("--systems", nargs="*", default=["pan_skin", "hematopoiesis", "pancreas"])
ap.add_argument("--variants", nargs="*", default=["pca", "marker"])
args = ap.parse_args()
for sys_ in args.systems:
for var in args.variants:
process(sys_, var)
if __name__ == "__main__":
main()
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