| import pandas as pd | |
| import numpy as np | |
| import requests | |
| import time | |
| import json | |
| from pathlib import Path | |
| import matplotlib.pyplot as plt | |
| from sklearn.metrics import (roc_auc_score, average_precision_score, | |
| roc_curve, precision_recall_curve) | |
| from sklearn.preprocessing import StandardScaler | |
| from sklearn.decomposition import PCA | |
| import torch | |
| import torch.nn as nn | |
| import warnings | |
| warnings.filterwarnings('ignore') | |
| BASE_PATH = Path('/content/IDP') | |
| PATHS = { | |
| 'features': BASE_PATH / 'features', | |
| 'embeddings': BASE_PATH / 'embeddings', | |
| 'benchmark': BASE_PATH / 'results' / 'benchmark', | |
| 'figures': BASE_PATH / 'results' / 'figures', | |
| } | |
| PATHS['benchmark'].mkdir(parents=True, exist_ok=True) | |
| PATHS['figures'].mkdir(parents=True, exist_ok=True) | |
| device = torch.device('cuda' if torch.cuda.is_available() else 'cpu') | |
| df = pd.read_parquet(PATHS['features'] / 'features_classical_full.parquet') | |
| id_cols = ['mutation_idx', 'uniprot_acc', 'gene_symbol', 'position', | |
| 'wt_aa', 'mut_aa', 'label'] | |
| feature_cols = [c for c in df.columns if c not in id_cols] | |
| X_features = np.nan_to_num(df[feature_cols].values.astype(np.float32), | |
| nan=0.0, posinf=0.0, neginf=0.0) | |
| X_emb_raw = np.load(PATHS['embeddings'] / 'embeddings_combined_full.npy').astype(np.float32) | |
| y = df['label'].values | |
| proteins = df['uniprot_acc'].values | |
| print(f" Variants: {len(df)} | Proteins: {df['uniprot_acc'].nunique()}") | |
| PP_SIFT_CACHE = PATHS['benchmark'] / 'polyphen_sift_filtered.parquet' | |
| if PP_SIFT_CACHE.exists(): | |
| print(" ✓ PolyPhen-2/SIFT cache found — loading") | |
| df_pp_sift = pd.read_parquet(PP_SIFT_CACHE) | |
| else: | |
| our_variants = {} | |
| for _, row in df.iterrows(): | |
| acc = row['uniprot_acc'].split('-')[0] | |
| key = (acc, int(row['position']) + 1, row['wt_aa'], row['mut_aa']) | |
| our_variants[key] = row['uniprot_acc'] | |
| print(f" Lookup: {len(our_variants)} variants across " | |
| f"{df['uniprot_acc'].nunique()} proteins\n") | |
| session = requests.Session() | |
| session.headers.update({ | |
| "Accept": "application/json", | |
| "User-Agent": "research-query/1.0" | |
| }) | |
| collected = [] | |
| unique_accs = df['uniprot_acc'].unique() | |
| PARTIAL = PATHS['benchmark'] / 'pp_sift_partial.parquet' | |
| if PARTIAL.exists(): | |
| done_df = pd.read_parquet(PARTIAL) | |
| done_accs = set(done_df['uniprot_acc'].str.split('-').str[0]) | |
| print(f" Resuming — {len(done_accs)} proteins already fetched, " | |
| f"{done_df['polyphen2_score'].notna().sum()} PP2 hits so far") | |
| collected = done_df.to_dict('records') | |
| else: | |
| done_accs = set() | |
| todo_accs = [a for a in unique_accs if a.split('-')[0] not in done_accs] | |
| print(f" Fetching {len(todo_accs)} proteins from UniProt variation API …") | |
| for i, acc in enumerate(todo_accs): | |
| acc_bare = acc.split('-')[0] | |
| url = f"https://www.ebi.ac.uk/proteins/api/variation/{acc_bare}" | |
| pp2_hits = sift_hits = 0 | |
| for attempt in range(4): | |
| try: | |
| r = session.get(url, timeout=30) | |
| if r.status_code == 200: | |
| data = r.json() | |
| for feat in data.get('features', []): | |
| if feat.get('type') != 'VARIANT': | |
| continue | |
| pos_begin = feat.get('begin') | |
| wt_aa = feat.get('wildType', '') | |
| mut_aa = feat.get('alternativeSequence', '') | |
| if not pos_begin or not wt_aa or not mut_aa: | |
| continue | |
| if len(wt_aa) != 1 or len(mut_aa) != 1: | |
| continue | |
| try: | |
| pos_1 = int(pos_begin) | |
| except (ValueError, TypeError): | |
| continue | |
| key = (acc_bare, pos_1, wt_aa, mut_aa) | |
| if key not in our_variants: | |
| continue | |
| pp2_score = None | |
| sift_score = None | |
| for pred in feat.get('predictions', []): | |
| algo = pred.get('predAlgorithmNameType', '') | |
| score = pred.get('score') | |
| if score is None: | |
| continue | |
| if 'PolyPhen' in algo or 'polyphen' in algo.lower(): | |
| pp2_score = float(score) | |
| pp2_hits += 1 | |
| elif 'SIFT' in algo or 'sift' in algo.lower(): | |
| sift_score = float(score) | |
| sift_hits += 1 | |
| collected.append({ | |
| 'uniprot_acc': our_variants[key], | |
| 'position': pos_1 - 1, | |
| 'wt_aa': wt_aa, | |
| 'mut_aa': mut_aa, | |
| 'polyphen2_score': pp2_score, | |
| 'sift_score': sift_score, | |
| }) | |
| break | |
| elif r.status_code == 404: | |
| break | |
| elif r.status_code == 429: | |
| time.sleep(5 * (attempt + 1)) | |
| else: | |
| time.sleep(2 ** attempt) | |
| except requests.exceptions.Timeout: | |
| time.sleep(3) | |
| except Exception as e: | |
| time.sleep(2) | |
| time.sleep(0.2) | |
| if (i + 1) % 50 == 0: | |
| partial_df = pd.DataFrame(collected).drop_duplicates( | |
| subset=['uniprot_acc', 'position', 'wt_aa', 'mut_aa']) | |
| partial_df.to_parquet(PARTIAL, index=False) | |
| n_pp = partial_df['polyphen2_score'].notna().sum() | |
| n_sift = partial_df['sift_score'].notna().sum() | |
| print(f" … {i+1}/{len(todo_accs)} proteins | " | |
| f"variants matched: {len(partial_df)} | " | |
| f"PP2: {n_pp} | SIFT: {n_sift}") | |
| df_pp_sift = pd.DataFrame(collected).drop_duplicates( | |
| subset=['uniprot_acc', 'position', 'wt_aa', 'mut_aa']) | |
| df_pp_sift.to_parquet(PP_SIFT_CACHE, index=False) | |
| print(f"\n Matched variants: {len(df_pp_sift)}") | |
| print(f" PolyPhen-2: {df_pp_sift['polyphen2_score'].notna().sum()}") | |
| print(f" SIFT: {df_pp_sift['sift_score'].notna().sum()}") | |
| print("\n" + "=" * 60) | |
| print(" MERGING SCORES") | |
| print("=" * 60) | |
| df_am = pd.read_parquet(PATHS['benchmark'] / 'alphamissense_filtered.parquet') | |
| df_bench = df[id_cols].copy() | |
| df_bench = df_bench.merge( | |
| df_am[['uniprot_acc','position','wt_aa','mut_aa','am_pathogenicity']], | |
| on=['uniprot_acc','position','wt_aa','mut_aa'], how='left') | |
| df_bench = df_bench.merge( | |
| df_pp_sift[['uniprot_acc','position','wt_aa','mut_aa', | |
| 'polyphen2_score','sift_score']], | |
| on=['uniprot_acc','position','wt_aa','mut_aa'], how='left') | |
| df_bench['sift_score_inv'] = 1 - df_bench['sift_score'] | |
| print(f" AlphaMissense: {df_bench['am_pathogenicity'].notna().sum()} " | |
| f"({100*df_bench['am_pathogenicity'].notna().mean():.1f}%)") | |
| print(f" PolyPhen-2: {df_bench['polyphen2_score'].notna().sum()} " | |
| f"({100*df_bench['polyphen2_score'].notna().mean():.1f}%)") | |
| print(f" SIFT: {df_bench['sift_score_inv'].notna().sum()} " | |
| f"({100*df_bench['sift_score_inv'].notna().mean():.1f}%)") | |
| df_bench.to_parquet(PATHS['benchmark'] / 'benchmark_merged.parquet', index=False) | |
| class SimpleMLP(nn.Module): | |
| def __init__(self, d, h=256): | |
| super().__init__() | |
| self.net = nn.Sequential( | |
| nn.Linear(d,h), nn.ReLU(), nn.Dropout(0.3), | |
| nn.Linear(h,h//2), nn.ReLU(), nn.Dropout(0.2), | |
| nn.Linear(h//2,1), nn.Sigmoid()) | |
| def forward(self, x): return self.net(x).squeeze() | |
| def prepare(Xf, Xe, tr, te, n=128): | |
| sf = StandardScaler() | |
| Xf_tr = sf.fit_transform(Xf[tr]); Xf_te = sf.transform(Xf[te]) | |
| pca = PCA(n_components=min(n, Xe[tr].shape[0]-1), random_state=42) | |
| Xp_tr = pca.fit_transform(Xe[tr]); Xp_te = pca.transform(Xe[te]) | |
| se = StandardScaler() | |
| Xe_tr = se.fit_transform(Xp_tr); Xe_te = se.transform(Xp_te) | |
| return (np.c_[Xf_tr,Xe_tr].astype(np.float32), | |
| np.c_[Xf_te,Xe_te].astype(np.float32)) | |
| def train_pred(Xtr, ytr, Xte, epochs=50): | |
| m = SimpleMLP(Xtr.shape[1]).to(device) | |
| opt = torch.optim.Adam(m.parameters(), lr=0.001, weight_decay=1e-4) | |
| crit = nn.BCELoss() | |
| Xt = torch.FloatTensor(Xtr).to(device) | |
| yt = torch.FloatTensor(ytr).to(device) | |
| Xv = torch.FloatTensor(Xte).to(device) | |
| m.train() | |
| for _ in range(epochs): | |
| opt.zero_grad(); crit(m(Xt), yt).backward(); opt.step() | |
| m.eval() | |
| with torch.no_grad(): return m(Xv).cpu().numpy() | |
| OUR_CACHE = PATHS['benchmark'] / 'our_model_lpocv_preds.npy' | |
| if OUR_CACHE.exists(): | |
| print("\n ✓ Model predictions cache found") | |
| our_preds = np.load(OUR_CACHE) | |
| else: | |
| our_preds = np.full(len(df), np.nan) | |
| ups = np.unique(proteins) | |
| print(f"\n Running LPOCV ({len(ups)} proteins) …") | |
| for i, p in enumerate(ups): | |
| te = proteins == p; tr = ~te | |
| if te.sum() < 2 or tr.sum() < 10: continue | |
| Xtr, Xte = prepare(X_features, X_emb_raw, tr, te) | |
| our_preds[te] = train_pred(Xtr, y[tr], Xte) | |
| if i % 50 == 0: print(f" … {i}/{len(ups)} proteins") | |
| np.save(OUR_CACHE, our_preds) | |
| print(" Saved") | |
| df_bench['our_score'] = our_preds | |
| tools = { | |
| 'Our model (MLP + ESM-2)': 'our_score', | |
| 'AlphaMissense': 'am_pathogenicity', | |
| 'PolyPhen-2': 'polyphen2_score', | |
| 'SIFT (inverted)': 'sift_score_inv', | |
| } | |
| results = {} | |
| for name, col in tools.items(): | |
| mask = df_bench[col].notna() & df_bench['our_score'].notna() | |
| sub = df_bench[mask] | |
| if len(sub) < 50: | |
| print(f" ⚠ {name}: only {len(sub)} variants — skipping") | |
| continue | |
| results[name] = { | |
| 'auc_roc': roc_auc_score(sub['label'], sub[col]), | |
| 'auc_pr': average_precision_score(sub['label'], sub[col]), | |
| 'n': len(sub), 'col': col, 'mask': mask} | |
| print(f" {name:<35} n={len(sub):>6,} " | |
| f"AUC-ROC={results[name]['auc_roc']:.3f} " | |
| f"AUC-PR={results[name]['auc_pr']:.3f}") |