"""Export all plotting CSVs for each figure into benchmark/figure_data/.""" from pathlib import Path import pandas as pd import numpy as np import shutil BENCH = Path(__file__).resolve().parents[1] FIGDATA = BENCH / "figure_data" FIGDATA.mkdir(exist_ok=True) TARGETS = ["PDL1", "MDM2", "IL23R"] def main(): # ── fig_ablation_bo_tradeoff ── ablation = pd.read_csv(BENCH / "ablation" / "ablation_summary_pose_filtered.csv") ablation.to_csv(FIGDATA / "fig_ablation_bo_tradeoff_ablation_summary.csv", index=False) tradeoff = pd.read_csv(BENCH / "ablation" / "ablation_tradeoff_pose_filtered.csv") tradeoff.to_csv(FIGDATA / "fig_ablation_bo_tradeoff_tradeoff.csv", index=False) bad = pd.read_csv(BENCH / "buried_pose_inventory.csv") # Ablation Tier-1 reuses the dl D-peptide designs, so the ablation bad-pose # counts are the D_peptide buried poses per core target. bad_ab = bad[bad["peptide_mode"] == "D_peptide"] bad_counts = ( bad_ab.groupby("target") .size() .reindex(TARGETS, fill_value=0) .rename("n_bad_poses") .reset_index() ) bad_counts.to_csv(FIGDATA / "fig_ablation_bo_tradeoff_bad_pose_counts.csv", index=False) print( f"fig_ablation: {len(ablation)} summary rows + " f"{len(tradeoff)} trade-off rows + {len(bad_counts)} pose counts" ) # ── fig_dl_score_distribution ── for t in TARGETS: for m in ["D_peptide", "L_peptide"]: src = BENCH / "dl_downsampled" / f"{t}_{m}_filtered.csv" dst = FIGDATA / f"fig_dl_score_dist_{t}_{m}.csv" shutil.copy2(src, dst) from scipy import stats as sp_stats rows = [] for t in TARGETS: d = pd.read_csv(FIGDATA / f"fig_dl_score_dist_{t}_D_peptide.csv") l = pd.read_csv(FIGDATA / f"fig_dl_score_dist_{t}_L_peptide.csv") ks, p = sp_stats.ks_2samp(d["score"], l["score"]) rows.append( { "target": t, "n": len(d), "D_median": d["score"].median(), "L_median": l["score"].median(), "D_mean": d["score"].mean(), "L_mean": l["score"].mean(), "KS_stat": ks, "KS_p": p, } ) pd.DataFrame(rows).to_csv(FIGDATA / "fig_dl_score_dist_summary.csv", index=False) print("fig_dl_score_dist: 6 CSVs + summary") # ── fig_dl_sequence_comparison (t-SNE top-100) ── from sklearn.decomposition import PCA from sklearn.manifold import TSNE AAS = list("ACDEFGHIKLMNPQRSTVWY") TOP_N = 100 aa2i = {a: i for i, a in enumerate(AAS)} def onehot(seqs, max_len): vecs = [] for s in seqs: v = np.zeros(max_len * len(AAS)) for pos, aa in enumerate(str(s)): if aa in aa2i: v[pos * len(AAS) + aa2i[aa]] = 1.0 vecs.append(v) return np.array(vecs) for t in TARGETS: d_df = pd.read_csv(FIGDATA / f"fig_dl_score_dist_{t}_D_peptide.csv") l_df = pd.read_csv(FIGDATA / f"fig_dl_score_dist_{t}_L_peptide.csv") d_top = d_df.nsmallest(TOP_N, "score").drop_duplicates("sequence").copy() l_top = l_df.nsmallest(TOP_N, "score").drop_duplicates("sequence").copy() ml = max(d_top["sequence"].str.len().max(), l_top["sequence"].str.len().max()) dv = onehot(d_top["sequence"], ml) lv = onehot(l_top["sequence"], ml) X = np.vstack([dv, lv]) npc = min(50, X.shape[1], X.shape[0] - 1) Xp = PCA(n_components=npc, random_state=42).fit_transform(X) Xt = TSNE( n_components=2, perplexity=30, random_state=42, learning_rate="auto", init="pca", ).fit_transform(Xp) nd = len(dv) d_out = d_top[["sequence", "score", "length", "pose"]].copy() d_out["tsne_1"] = Xt[:nd, 0] d_out["tsne_2"] = Xt[:nd, 1] d_out["type"] = "D" l_out = l_top[["sequence", "score", "length", "pose"]].copy() l_out["tsne_1"] = Xt[nd:, 0] l_out["tsne_2"] = Xt[nd:, 1] l_out["type"] = "L" combined = pd.concat([d_out, l_out], ignore_index=True) combined.to_csv(FIGDATA / f"fig_dl_tsne_{t}.csv", index=False) print(f"fig_dl_tsne_{t}: {nd} D + {len(l_out)} L = {len(combined)} rows") print(f"\nAll figure data saved to {FIGDATA}/") for f in sorted(FIGDATA.iterdir()): print(f" {f.name} ({f.stat().st_size/1024:.1f} KB)") if __name__ == "__main__": main()