IDP-Pathogenicity-Model / scripts /models_comparaison.py
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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}")