Side-Info_Generation / src /visualize_features.py
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import os
import torch
import pandas as pd
import numpy as np
import matplotlib
matplotlib.use('Agg')
import matplotlib.pyplot as plt
import seaborn as sns
from sklearn.decomposition import PCA
from sklearn.metrics import silhouette_score
from torch.utils.data import DistributedSampler
from torchvision.datasets import ImageFolder
PLOTS_DIR = 'plots'
os.makedirs(PLOTS_DIR, exist_ok=True)
# 1. Reconstruct dataset file names matching the DistributedSampler order
print("Reconstructing dataset file list and sampler indices...")
dataset = ImageFolder('data/images/val')
sampler = DistributedSampler(dataset, num_replicas=1, rank=0)
indices = list(sampler)
# Get the list of file names in the exact sampler order
sampler_filenames = [dataset.imgs[idx][0] for idx in indices]
# Convert absolute/relative paths to match the parquet file_name column (e.g. val/class/file.jpg)
# dataset.imgs paths look like: 'data/images/val/03368_.../file.jpg'
cleaned_filenames = []
for p in sampler_filenames:
parts = p.split(os.sep)
# Find where 'val' starts
if 'val' in parts:
val_idx = parts.index('val')
cleaned_filenames.append('/'.join(parts[val_idx:]))
else:
cleaned_filenames.append(p)
# 2. Load metadata and align
print("Loading and aligning metadata...")
df = pd.read_parquet('metadata/inat_world_model_master.parquet')
df_val = df[df['split'] == 'val'].copy()
df_val.set_index('file_name', inplace=True)
# Reorder metadata to match the sampler order
aligned_meta = []
for fname in cleaned_filenames:
if fname in df_val.index:
# If there are duplicates, take the first one
row = df_val.loc[fname]
if isinstance(row, pd.DataFrame):
row = row.iloc[0]
aligned_meta.append(row.to_dict())
else:
# Fallback empty dict
aligned_meta.append({})
df_aligned = pd.DataFrame(aligned_meta)
# Drop rows where we have missing lifestyle/trophic level metadata
valid_mask = df_aligned['Primary.Lifestyle'].notna() & df_aligned['Trophic.Level'].notna()
print(f"Aligned metadata rows: {len(df_aligned)}, Valid rows for analysis: {valid_mask.sum()}")
# 3. Load embeddings
models_config = {
'DINOv3': {
'path': 'outputs/vit_large_patch16_dinov3/macro_val_30percent_rank_0.pt',
'safe_name': 'vit_large_patch16_dinov3'
},
'SigLIP2': {
'path': 'outputs/google_siglip2_so400m_patch14_384/macro_val_30percent_rank_0.pt',
'safe_name': 'google_siglip2_so400m_patch14_384'
},
'BioCLIP2': {
'path': 'outputs/hf_hub:imageomics_bioclip_2.5_vith14/macro_val_30percent_rank_0.pt',
'safe_name': 'hf_hub:imageomics_bioclip_2.5_vith14'
}
}
embeddings_data = {}
for name, cfg in models_config.items():
if os.path.exists(cfg['path']):
print(f"Loading {name} embeddings from {cfg['path']}...")
data = torch.load(cfg['path'], map_location='cpu')
embeddings = data['embeddings'].numpy()
embeddings_data[name] = embeddings
else:
print(f"Warning: {cfg['path']} does not exist!")
# Subset metadata to match the length of the 30% macro files
# The 30% macro file contains exactly the first 30% of the validation set batches
n_samples = None
for name, embs in embeddings_data.items():
n_samples = len(embs)
break
if n_samples is None:
print("Error: No embeddings loaded. Exiting.")
exit(1)
print(f"Analyzing first {n_samples} samples...")
df_subset = df_aligned.iloc[:n_samples].copy()
valid_mask_sub = valid_mask.iloc[:n_samples].values
# Filter out rows with invalid metadata from both embeddings and metadata
df_filtered = df_subset[valid_mask_sub].copy()
# Apply PCA and calculate Silhouette Scores
results = {}
for name, embs in embeddings_data.items():
embs_filtered = embs[valid_mask_sub]
# 2D PCA Projection
print(f"Running PCA for {name}...")
pca = PCA(n_components=2, random_state=42)
coords = pca.fit_transform(embs_filtered)
# Calculate Silhouette Scores on the full-dimensional embeddings
print(f"Calculating Silhouette Scores for {name}...")
sil_lifestyle = silhouette_score(embs_filtered, df_filtered['Primary.Lifestyle'].astype(str))
sil_trophic = silhouette_score(embs_filtered, df_filtered['Trophic.Level'].astype(str))
results[name] = {
'coords': coords,
'sil_lifestyle': sil_lifestyle,
'sil_trophic': sil_trophic
}
# 4. Generate the 2x3 Plot Grid
sns.set_theme(style="whitegrid")
fig, axes = plt.subplots(2, 3, figsize=(18, 11))
for col_idx, model_name in enumerate(results.keys()):
res = results[model_name]
coords = res['coords']
# Row 1: Primary Lifestyle
ax1 = axes[0, col_idx]
sns.scatterplot(
x=coords[:, 0], y=coords[:, 1],
hue=df_filtered['Primary.Lifestyle'],
palette='Set1', alpha=0.5, s=8, ax=ax1, legend=(col_idx == 2)
)
ax1.set_title(f"{model_name}\nLifestyle Silhouette: {res['sil_lifestyle']:.3f}")
if col_idx == 2:
ax1.legend(title='Primary Lifestyle', bbox_to_anchor=(1.05, 1), loc='upper left')
ax1.set_xlabel("PCA 1")
ax1.set_ylabel("PCA 2")
# Row 2: Trophic Level
ax2 = axes[1, col_idx]
sns.scatterplot(
x=coords[:, 0], y=coords[:, 1],
hue=df_filtered['Trophic.Level'],
palette='Dark2', alpha=0.5, s=8, ax=ax2, legend=(col_idx == 2)
)
ax2.set_title(f"Trophic Level Silhouette: {res['sil_trophic']:.3f}")
if col_idx == 2:
ax2.legend(title='Trophic Level', bbox_to_anchor=(1.05, 1), loc='upper left')
ax2.set_xlabel("PCA 1")
ax2.set_ylabel("PCA 2")
plt.suptitle("Model Feature Space Representation vs. Ecological Metadata", y=0.98, fontsize=16, fontweight='bold')
plt.tight_layout()
fig.savefig(os.path.join(PLOTS_DIR, 'feature_representation_comparison.png'), bbox_inches='tight', dpi=200)
plt.close(fig)
print("\n=== SILHOUETTE SCORE SUMMARY ===")
for name, res in results.items():
print(f"{name}:")
print(f" Primary Lifestyle Silhouette Score: {res['sil_lifestyle']:.4f}")
print(f" Trophic Level Silhouette Score: {res['sil_trophic']:.4f}")
print("\nPlots generated successfully at plots/feature_representation_comparison.png")