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"""Head-to-head comparison: scPTR vs scVelo vs velVI.
Compares degradation rate / kinetic parameter estimates across methods
using the same evaluation framework:
1. Half-life correlation (mouse + human references)
2. Cell-type discrimination (silhouette, ANOVA F-stat)
3. Latent quality (pseudotime correlation, cell-type silhouette)
4. Runtime
Datasets: pancreas, dentate gyrus.
"""
from _common import *
import scanpy as sc
import scvelo as scv
import time as _time
from sklearn.metrics import silhouette_score
from sklearn.decomposition import PCA
OUT = output_dir("12_method_comparison")
# ββ scVelo steady-state ββββββββββββββββββββββββββββββββββββββββββββββββββββ
def run_scvelo_steady(adata_raw, name):
"""Run scVelo steady-state mode, extract gamma-like parameter."""
print(f"\n scVelo steady-state ({name})...")
adata = adata_raw.copy()
t0 = _time.time()
scv.pp.filter_and_normalize(adata, min_shared_counts=20, n_top_genes=2000)
scv.pp.moments(adata, n_pcs=30, n_neighbors=30)
scv.tl.velocity(adata, mode="steady_state")
scv.tl.velocity_graph(adata)
elapsed = _time.time() - t0
# scVelo stores velocity_gamma in adata.var
# gamma_ss = fit parameter from u = gamma * s + offset
gamma = adata.var.get("velocity_gamma", pd.Series(dtype=float))
# For cell-type discrimination, use velocity PCA
if "velocity" in adata.layers:
vel = np.asarray(adata.layers["velocity"])
vel = np.nan_to_num(vel, 0)
vel_pca = PCA(n_components=min(10, vel.shape[1])).fit_transform(vel)
else:
vel_pca = None
print(f" Done in {elapsed:.1f}s, {len(gamma)} genes, {adata.n_vars} after filter")
return adata, gamma, vel_pca, elapsed
# ββ scVelo dynamical ββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def run_scvelo_dynamical(adata_raw, name):
"""Run scVelo dynamical mode, extract gamma and latent time."""
print(f"\n scVelo dynamical ({name})...")
adata = adata_raw.copy()
t0 = _time.time()
scv.pp.filter_and_normalize(adata, min_shared_counts=20, n_top_genes=2000)
scv.pp.moments(adata, n_pcs=30, n_neighbors=30)
scv.tl.recover_dynamics(adata, n_jobs=4)
scv.tl.velocity(adata, mode="dynamical")
scv.tl.velocity_graph(adata)
scv.tl.latent_time(adata)
elapsed = _time.time() - t0
gamma = adata.var.get("fit_gamma", pd.Series(dtype=float))
latent_time = adata.obs.get("latent_time", pd.Series(dtype=float))
if "velocity" in adata.layers:
vel = np.asarray(adata.layers["velocity"])
vel = np.nan_to_num(vel, 0)
vel_pca = PCA(n_components=min(10, vel.shape[1])).fit_transform(vel)
else:
vel_pca = None
print(f" Done in {elapsed:.1f}s, {len(gamma)} genes")
return adata, gamma, latent_time, vel_pca, elapsed
# ββ velVI βββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def run_velovi(adata_raw, name):
"""Run velVI (VELOVI from scvi-tools)."""
print(f"\n velVI ({name})...")
from scvi.external import VELOVI
adata = adata_raw.copy()
t0 = _time.time()
# Preprocessing (velVI needs spliced/unspliced in layers + scVelo moments)
scv.pp.filter_and_normalize(adata, min_shared_counts=20, n_top_genes=1000)
scv.pp.moments(adata, n_pcs=30, n_neighbors=30)
# Setup and train (CPU β CUDA kernel incompatible on this system)
VELOVI.setup_anndata(adata, spliced_layer="Ms", unspliced_layer="Mu")
model = VELOVI(adata, n_latent=10, n_hidden=128, n_layers=1)
model.train(max_epochs=50, early_stopping=True, early_stopping_patience=10,
accelerator="cpu")
elapsed = _time.time() - t0
# Extract latent representation
latent = model.get_latent_representation()
adata.obsm["X_velovi"] = latent
# Extract per-gene parameters
# velVI stores gamma-like parameters internally
# Get velocity outputs
try:
outputs = model.get_velocity()
if "velocity" not in adata.layers:
adata.layers["velocity"] = outputs
except Exception:
pass
# velVI gamma from the model
gamma_vals = None
try:
gamma_vals = model.get_rates()
if isinstance(gamma_vals, dict) and "gamma" in gamma_vals:
gamma_vals = gamma_vals["gamma"]
except Exception:
pass
vel_pca = None
if "velocity" in adata.layers:
vel = np.asarray(adata.layers["velocity"])
vel = np.nan_to_num(vel, 0)
vel_pca = PCA(n_components=min(10, vel.shape[1])).fit_transform(vel)
print(f" Done in {elapsed:.1f}s")
return adata, gamma_vals, latent, vel_pca, elapsed
# ββ scPTR analytical ββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def run_scptr_analytical(adata_raw, name):
"""Run scPTR analytical pipeline."""
print(f"\n scPTR analytical ({name})...")
adata = adata_raw.copy()
t0 = _time.time()
scptr.pp.filter_genes(adata)
scptr.pp.normalize_layers(adata)
scptr.pp.neighbors(adata, n_neighbors=30)
scptr.pp.smooth_layers(adata)
scptr.tl.estimate_beta(adata)
scptr.tl.estimate_gamma(adata)
elapsed = _time.time() - t0
gamma_med = np.median(adata.layers["gamma"], axis=0)
gamma_s = pd.Series(gamma_med, index=adata.var_names)
# Gamma PCA for cell-type discrimination
gamma_pca = PCA(n_components=min(10, adata.layers["gamma"].shape[1])).fit_transform(
adata.layers["gamma"]
)
print(f" Done in {elapsed:.1f}s, {adata.n_vars} genes")
return adata, gamma_s, gamma_pca, elapsed
# ββ scPTR DeepPTR βββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def run_scptr_deep(adata_raw, name):
"""Run DeepPTR."""
print(f"\n DeepPTR ({name})...")
adata = adata_raw.copy()
t0 = _time.time()
scptr.pp.filter_genes(adata)
scptr.pp.normalize_layers(adata)
scptr.pp.neighbors(adata, n_neighbors=30)
scptr.pp.smooth_layers(adata)
scptr.tl.estimate_beta(adata)
adata = select_top_genes(adata, n_top=300)
torch.set_num_threads(4)
model, history = scptr.deep.fit_deepptr(adata, verbose=False, **DEEP_HP)
elapsed = _time.time() - t0
gamma_med = np.median(adata.layers["gamma"], axis=0)
gamma_s = pd.Series(gamma_med, index=adata.var_names)
print(f" Done in {elapsed:.1f}s, {adata.n_vars} genes")
return adata, gamma_s, adata.obsm.get("X_z_T"), elapsed
# ββ Evaluation ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def eval_halflife(gamma_series_or_adata, hl_df, method_name):
"""Evaluate half-life correlation for any method's gamma estimates."""
if isinstance(gamma_series_or_adata, pd.Series):
gamma_s = gamma_series_or_adata
else:
# It's an adata with gamma layer
adata = gamma_series_or_adata
gamma_med = np.median(adata.layers["gamma"], axis=0)
gamma_s = pd.Series(gamma_med, index=adata.var_names)
hl_s = hl_df.set_index("gene_symbol")["half_life_hours"]
# Case-insensitive match
gamma_upper = {g.upper(): g for g in gamma_s.index}
hl_upper = {g.upper(): g for g in hl_s.index if isinstance(g, str)}
shared = set(gamma_upper.keys()) & set(hl_upper.keys())
g = np.array([gamma_s[gamma_upper[u]] for u in shared], dtype=float)
h = np.array([hl_s[hl_upper[u]] for u in shared], dtype=float)
valid = np.isfinite(g) & np.isfinite(h) & (g > 0) & (h > 0)
if valid.sum() < 3:
return np.nan, 0
r, _ = stats.spearmanr(g[valid], h[valid])
return float(r), int(valid.sum())
def eval_celltype(latent_or_pca, labels, method_name):
"""Evaluate cell-type discrimination in latent/kinetic space."""
if latent_or_pca is None:
return np.nan
labels_arr = np.asarray(labels)
if isinstance(labels_arr[0], str):
from sklearn.preprocessing import LabelEncoder
labels_arr = LabelEncoder().fit_transform(labels_arr)
n_sample = min(2000, len(labels_arr))
try:
return float(silhouette_score(latent_or_pca, labels_arr, sample_size=n_sample))
except Exception:
return np.nan
def eval_anova_fstat(gamma_matrix, labels, gene_names):
"""Median F-statistic across genes for cell-type gamma differences."""
from scipy.stats import f_oneway
cts = sorted(set(labels))
f_stats = []
for g in range(gamma_matrix.shape[1]):
groups = [gamma_matrix[labels == ct, g] for ct in cts if (labels == ct).sum() >= 5]
if len(groups) < 2:
continue
try:
f, p = f_oneway(*groups)
if np.isfinite(f):
f_stats.append(f)
except Exception:
pass
return float(np.median(f_stats)) if f_stats else np.nan
# ββ Main comparison βββββββββββββββββββββββββββββββββββββββββββββββββββββββ
def run_comparison(name, loader, cluster_key):
print(f"\n{'#' * 60}")
print(f"# {name.upper()}: METHOD COMPARISON")
print(f"{'#' * 60}")
adata_raw = loader()
hl_mouse, hl_human = load_halflife_refs()
labels = adata_raw.obs.get(cluster_key, pd.Series(dtype=str)).values
results = {}
# ββ Run each method βββββββββββββββββββββββββββββββββββββββββββββββ
# 1. scVelo steady-state
try:
sv_ss_adata, sv_ss_gamma, sv_ss_pca, sv_ss_time = run_scvelo_steady(adata_raw, name)
results["scvelo_ss"] = {"time": sv_ss_time, "n_genes": len(sv_ss_gamma)}
except Exception as e:
print(f" scVelo SS failed: {e}")
sv_ss_gamma, sv_ss_pca = pd.Series(dtype=float), None
results["scvelo_ss"] = {"error": str(e)}
# 2. scVelo dynamical
try:
sv_dyn_adata, sv_dyn_gamma, sv_dyn_ltime, sv_dyn_pca, sv_dyn_time = run_scvelo_dynamical(adata_raw, name)
results["scvelo_dyn"] = {"time": sv_dyn_time, "n_genes": len(sv_dyn_gamma)}
except Exception as e:
print(f" scVelo dyn failed: {e}")
sv_dyn_gamma, sv_dyn_ltime, sv_dyn_pca = pd.Series(dtype=float), None, None
results["scvelo_dyn"] = {"error": str(e)}
# 3. velVI
try:
vi_adata, vi_gamma, vi_latent, vi_pca, vi_time = run_velovi(adata_raw, name)
results["velovi"] = {"time": vi_time}
except Exception as e:
print(f" velVI failed: {e}")
vi_gamma, vi_latent, vi_pca = None, None, None
results["velovi"] = {"error": str(e)}
# 4. scPTR analytical
sp_adata, sp_gamma, sp_pca, sp_time = run_scptr_analytical(adata_raw, name)
results["scptr_analytical"] = {"time": sp_time, "n_genes": len(sp_gamma)}
# 5. DeepPTR
dp_adata, dp_gamma, dp_latent, dp_time = run_scptr_deep(adata_raw, name)
results["deepptr"] = {"time": dp_time, "n_genes": len(dp_gamma)}
# ββ Evaluate: half-life correlations βββββββββββββββββββββββββββββ
print(f"\n--- Half-life correlations ---")
methods_gamma = {
"scVelo SS": sv_ss_gamma,
"scVelo dyn": sv_dyn_gamma,
"scPTR analytical": sp_gamma,
"DeepPTR": dp_gamma,
}
for ref_name, hl_df in [("mouse", hl_mouse), ("human", hl_human)]:
print(f"\n {ref_name}:")
for mname, gamma in methods_gamma.items():
if gamma is not None and len(gamma) > 0:
r, n = eval_halflife(gamma, hl_df, mname)
results.setdefault(mname.lower().replace(" ", "_"), {})
results[mname.lower().replace(" ", "_")][f"halflife_{ref_name}"] = {"r": r, "n": n}
print(f" {mname:25s}: r={r:.4f} (n={n})")
else:
print(f" {mname:25s}: N/A")
# velVI (if gamma available as pd.Series or array)
if vi_gamma is not None:
if isinstance(vi_gamma, np.ndarray) and vi_gamma.ndim == 1:
# Try to match with velVI adata gene names
try:
vi_gs = pd.Series(vi_gamma, index=vi_adata.var_names)
r, n = eval_halflife(vi_gs, hl_df, "velVI")
except Exception:
r, n = np.nan, 0
elif isinstance(vi_gamma, pd.Series):
r, n = eval_halflife(vi_gamma, hl_df, "velVI")
else:
r, n = np.nan, 0
results.setdefault("velovi", {})
results["velovi"][f"halflife_{ref_name}"] = {"r": r, "n": n}
print(f" {'velVI':25s}: r={r:.4f} (n={n})")
# ββ Evaluate: cell-type discrimination ββββββββββββββββββββββββββββ
print(f"\n--- Cell-type discrimination (silhouette) ---")
if cluster_key in adata_raw.obs.columns:
spaces = {
"scVelo SS velocity": sv_ss_pca,
"scVelo dyn velocity": sv_dyn_pca,
"velVI latent": vi_latent,
"velVI velocity": vi_pca,
"scPTR gamma": sp_pca,
"DeepPTR z_T": dp_latent,
}
for sname, space in spaces.items():
if space is not None:
# Need matching labels
if "scVelo" in sname:
if "SS" in sname:
lbl = sv_ss_adata.obs.get(cluster_key, pd.Series(dtype=str)).values
else:
lbl = sv_dyn_adata.obs.get(cluster_key, pd.Series(dtype=str)).values
elif "velVI" in sname:
lbl = vi_adata.obs.get(cluster_key, pd.Series(dtype=str)).values
elif "scPTR" in sname:
lbl = sp_adata.obs.get(cluster_key, pd.Series(dtype=str)).values
else:
lbl = dp_adata.obs.get(cluster_key, pd.Series(dtype=str)).values
sil = eval_celltype(space, lbl, sname)
key = sname.lower().replace(" ", "_")
results[key] = results.get(key, {})
results[key]["silhouette"] = sil
print(f" {sname:25s}: {sil:.4f}")
# ββ Evaluate: ANOVA F-stat on scPTR gamma βββββββββββββββββββββββββ
print(f"\n--- Gamma cell-type F-statistic ---")
if cluster_key in sp_adata.obs.columns:
f_an = eval_anova_fstat(sp_adata.layers["gamma"],
sp_adata.obs[cluster_key].values,
sp_adata.var_names)
f_dp = eval_anova_fstat(dp_adata.layers["gamma"],
dp_adata.obs[cluster_key].values,
dp_adata.var_names)
print(f" scPTR analytical: median F = {f_an:.2f}")
print(f" DeepPTR: median F = {f_dp:.2f}")
results["gamma_fstat"] = {"analytical": f_an, "deepptr": f_dp}
# ββ Runtime comparison ββββββββββββββββββββββββββββββββββββββββββββ
print(f"\n--- Runtime ---")
runtimes = {
"scVelo SS": results.get("scvelo_ss", {}).get("time", np.nan),
"scVelo dyn": results.get("scvelo_dyn", {}).get("time", np.nan),
"velVI": results.get("velovi", {}).get("time", np.nan),
"scPTR analytical": results.get("scptr_analytical", {}).get("time", np.nan),
"DeepPTR": results.get("deepptr", {}).get("time", np.nan),
}
for mname, t in runtimes.items():
print(f" {mname:25s}: {t:.1f}s" if np.isfinite(t) else f" {mname:25s}: N/A")
save_json(results, f"{name}_comparison", OUT)
# ββ Summary figure ββββββββββββββββββββββββββββββββββββββββββββββββ
fig, axes = plt.subplots(1, 3, figsize=(16, 5))
# Panel 1: Half-life correlation
methods = ["scVelo SS", "scVelo dyn", "scPTR analytical", "DeepPTR"]
method_keys = ["scvelo_ss", "scvelo_dyn", "scptr_analytical", "deepptr"]
colors = ["#1f77b4", "#2ca02c", "#ff7f0e", "#d62728"]
for ref_idx, ref_name in enumerate(["mouse", "human"]):
x_offset = ref_idx * 0.4
for i, (mname, mkey) in enumerate(zip(methods, method_keys)):
r = results.get(mkey, {}).get(f"halflife_{ref_name}", {}).get("r", np.nan)
if np.isfinite(r):
axes[0].bar(i + x_offset, abs(r), 0.35, color=colors[i],
alpha=0.7 if ref_idx == 0 else 0.4)
axes[0].set_xticks(range(len(methods)))
axes[0].set_xticklabels(methods, rotation=30, ha="right", fontsize=8)
axes[0].set_ylabel("|Spearman r| with half-life")
axes[0].set_title(f"{name}: Half-life correlation")
# Panel 2: Runtime
valid_runtimes = {k: v for k, v in runtimes.items() if np.isfinite(v)}
if valid_runtimes:
axes[1].barh(list(valid_runtimes.keys()), list(valid_runtimes.values()),
color=colors[:len(valid_runtimes)], alpha=0.7)
axes[1].set_xlabel("Runtime (seconds)")
axes[1].set_title("Runtime comparison")
# Panel 3: Silhouette scores
sil_data = {}
for sname in ["scVelo SS velocity", "scVelo dyn velocity", "scPTR gamma", "DeepPTR z_T"]:
key = sname.lower().replace(" ", "_")
s = results.get(key, {}).get("silhouette", np.nan)
if np.isfinite(s):
sil_data[sname] = s
if sil_data:
axes[2].bar(list(sil_data.keys()), list(sil_data.values()), color="steelblue", alpha=0.7)
axes[2].set_ylabel("Silhouette score")
axes[2].set_title("Cell-type discrimination")
plt.setp(axes[2].get_xticklabels(), rotation=30, ha="right", fontsize=8)
fig.suptitle(f"{name}: Method comparison", y=1.02)
fig.tight_layout()
save_fig(fig, f"{name}_method_comparison", OUT)
return results
def main():
set_figure_style()
all_results = {}
for name, loader, ck in DATASETS:
all_results[name] = run_comparison(name, loader, ck)
# Print summary table
print(f"\n{'=' * 80}")
print("METHOD COMPARISON SUMMARY")
print("=" * 80)
print(f"\n{'Method':<25} {'HL mouse':>10} {'HL human':>10} {'Runtime':>10}")
print("-" * 60)
for ds_name in all_results:
print(f"\n {ds_name.upper()}")
r = all_results[ds_name]
for mkey, mname in [("scvelo_ss", "scVelo SS"), ("scvelo_dyn", "scVelo dyn"),
("velovi", "velVI"),
("scptr_analytical", "scPTR analytical"), ("deepptr", "DeepPTR")]:
d = r.get(mkey, {})
r_m = d.get("halflife_mouse", {}).get("r", np.nan)
r_h = d.get("halflife_human", {}).get("r", np.nan)
t = d.get("time", np.nan)
r_m_s = f"{r_m:.4f}" if np.isfinite(r_m) else "N/A"
r_h_s = f"{r_h:.4f}" if np.isfinite(r_h) else "N/A"
t_s = f"{t:.0f}s" if np.isfinite(t) else "N/A"
print(f" {mname:<25} {r_m_s:>10} {r_h_s:>10} {t_s:>10}")
save_json(all_results, "comparison_all", OUT)
if __name__ == "__main__":
main()
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