File size: 8,322 Bytes
b46126b
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
import numpy as np
import torch
import torch.nn as nn
import torch.nn.functional as F
from torch.utils.data import Dataset, DataLoader, RandomSampler

# =====================
# 1. SETUP & DATA LOADING
# =====================
print("Loading sequence / phyloP data...")

dna_path = "/home/n5huang/dna_token/SparseAE/chr1_dna.txt"
phy_path = "/home/n5huang/dna_token/SparseAE/chr1_phyloP_norm.npy"

with open(dna_path) as f:
    sequence = f.read().strip()

phy_norm = np.load(phy_path)

assert len(sequence) == len(phy_norm), "DNA and phyloP length mismatch!"
chrom_len = len(sequence)
print(f"Chromosome 1 length: {chrom_len:,} bp")

# =====================
# 2. DNA ENCODING (HANDLE 'N')
# =====================
print("Encoding DNA to one-hot (with N handling)...")

mapping = {'A': 0, 'C': 1, 'G': 2, 'T': 3}

# Map bases to ints, using 4 as "N/unknown"
dna_int = np.fromiter((mapping.get(b, 4) for b in sequence), dtype=np.int8)
num_N = np.sum(dna_int == 4)
print(f"Number of N bases: {num_N:,}")

# One-hot with an extra row for N
# 0=A,1=C,2=G,3=T,4=[0,0,0,0,1]
temp_onehot = np.eye(5, dtype=np.float32)[dna_int]

# Slice to first 4 columns: N -> [0,0,0,0]
dna_onehot = temp_onehot[:, :4]   # shape (chrom_len, 4)

# =====================
# 3. PHYLOP CHECK + COMBINE
# =====================
print("Preparing combined tensor...")

# Assume phy_norm is already in [-1,1]; warn if not.
max_abs_phy = np.max(np.abs(phy_norm))
if max_abs_phy > 1.1:
    print(f"WARNING: phy_norm max abs={max_abs_phy:.3f} > 1.1; "
          f"data may not be normalized as expected.")

phy_norm = phy_norm.astype(np.float32)
phy_col = phy_norm.reshape(-1, 1)          # (chrom_len, 1)

combined_np = np.concatenate([dna_onehot, phy_col], axis=1)  # (chrom_len, 5)
combined_tensor = torch.from_numpy(combined_np)              # CPU tensor

print(f"Master tensor shape: {combined_tensor.shape}")

# =====================
# 4. DATASET: CHUNKED WINDOWING
# =====================
L = 50

class ChunkedChr1Dataset(Dataset):
    def __init__(self, combined, L=50):
        self.combined = combined
        self.L = L
        self.N = combined.shape[0] - L   # number of valid start positions

    def __len__(self):
        return self.N

    def __getitem__(self, idx):
        # window: (L, 5)
        window = self.combined[idx : idx + self.L]
        dna = window[:, :4]          # (L, 4)
        phy = window[:, 4]           # (L,)
        return dna, phy

dataset = ChunkedChr1Dataset(combined_tensor, L=L)
print(f"Dataset length (#windows): {len(dataset):,}")

# =====================
# 5. DATALOADER WITH RANDOM SAMPLER
# =====================
BATCH_SIZE = 1024
SAMPLES_PER_EPOCH = 5_000_000  # number of windows per epoch (tunable)

sampler = RandomSampler(
    dataset,
    replacement=True,
    num_samples=SAMPLES_PER_EPOCH
)

loader = DataLoader(
    dataset,
    batch_size=BATCH_SIZE,
    sampler=sampler,
    drop_last=True,
    num_workers=0,       # safer on large dataset
    pin_memory=True
)

print("DataLoader ready.")

# =====================
# 6. MODEL: SPARSE AUTOENCODER
# =====================
INPUT_DIM = L * 5      # 4 DNA + 1 phyloP
LATENT_DIM = 2048
HIDDEN_DIM = 1024

class SparseAE(nn.Module):
    def __init__(self, input_dim=INPUT_DIM, latent_dim=LATENT_DIM, hidden_dim=HIDDEN_DIM):
        super().__init__()

        # Encoder
        self.encoder = nn.Sequential(
            nn.Linear(input_dim, hidden_dim),
            nn.ReLU(),
            nn.Linear(hidden_dim, latent_dim),
            nn.ReLU()  # ReLU helps sparsity with L1
        )

        # Decoder shared
        self.dec_hidden = nn.Linear(latent_dim, hidden_dim)

        # Decoder heads
        self.dec_dna = nn.Linear(hidden_dim, L * 4)
        self.dec_phy = nn.Linear(hidden_dim, L * 1)

    def forward(self, dna, phy):
        B = dna.size(0)

        x = torch.cat(
            [dna.reshape(B, -1), phy.reshape(B, -1)],
            dim=1
        )  # (B, INPUT_DIM)

        h = self.encoder(x)
        dec = F.relu(self.dec_hidden(h))

        recon_dna = self.dec_dna(dec).reshape(B, L, 4)      # (B, L, 4)
        recon_phy = torch.tanh(self.dec_phy(dec)).reshape(B, L)  # (B, L)

        return recon_dna, recon_phy, h

# =====================
# 7. TRAINING LOOP
# =====================
device = "cuda" if torch.cuda.is_available() else "cpu"
print(f"Training on device: {device}")

model = SparseAE().to(device)
optimizer = torch.optim.Adam(model.parameters(), lr=1e-4)

#lambda_l1 = 0.01      # slightly stronger sparsity
lambda_l1_start = 0.02
lambda_l1_end   = 0.005
phy_weight = 10.0
num_epochs = 5
PRINT_EVERY = 1000    # batches
beta_kl_schedule = [0.0, 0.01, 0.02, 0.05, 0.1]   # per epoch



print("Starting training...")

for epoch in range(num_epochs):
    model.train()
    total_loss = 0.0
    total_dna = 0.0
    total_phy = 0.0
    total_active = 0.0

    batch_count = 0
    for dna_batch, phy_batch in loader:
        batch_count += 1

        dna_batch = dna_batch.to(device, non_blocking=True).float()  # (B, L, 4)
        phy_batch = phy_batch.to(device, non_blocking=True).float()  # (B, L)

        optimizer.zero_grad()

        recon_dna, recon_phy, h = model(dna_batch, phy_batch)

        # Mask positions that are 'N' (all-zero one-hot)
        mask = dna_batch.sum(dim=-1) > 0   # (B, L), True where valid base

        # --- DNA loss (masked CE) ---
        true_dna_cls = dna_batch.argmax(dim=-1)              # (B, L)
        dna_logits = recon_dna.permute(0, 2, 1)              # (B, 4, L)
        loss_dna_raw = F.cross_entropy(dna_logits, true_dna_cls, reduction='none')  # (B, L)

        if mask.sum() > 0:
            loss_dna = (loss_dna_raw * mask).sum() / mask.sum()
        else:
            loss_dna = torch.tensor(0.0, device=device)

        # --- PhyloP loss (masked MSE) ---
        loss_phy_raw = F.mse_loss(recon_phy, phy_batch, reduction='none')  # (B, L)

        if mask.sum() > 0:
            loss_phy = (loss_phy_raw * mask).sum() / mask.sum()
        else:
            loss_phy = torch.tensor(0.0, device=device)

        # --- KL sparsity penalty ---
        rho = 0.02   # target sparsity 
        eps = 1e-12
        rho_hat = torch.mean(h, dim=0)
        rho_hat = torch.clamp(rho_hat, min=1e-6, max=1-1e-6)
        kl_per_unit = (
            rho * torch.log((rho + eps) / (rho_hat + eps)) +
            (1 - rho) * torch.log(((1 - rho) + eps) / ((1 - rho_hat) + eps))
        )
        beta_kl = beta_kl_schedule[min(epoch, len(beta_kl_schedule)-1)]
        #loss_kl = 1 * kl_per_unit.sum()   # β = 1 regularization weight
        loss_kl = beta_kl * kl_per_unit.sum()


        lambda_l1 = (
            lambda_l1_start
            + (lambda_l1_end - lambda_l1_start) * (epoch / (num_epochs - 1))
        )

        # --- L1 sparsity on latent ---
        loss_l1 = lambda_l1 * torch.mean(torch.abs(h))

        # Total loss
        loss = loss_dna + phy_weight * loss_phy + loss_l1 + loss_kl

        loss.backward()
        optimizer.step()

        # Logging accumulators
        B = dna_batch.size(0)
        total_loss += loss.item() * B
        total_dna  += loss_dna.item() * B
        total_phy  += loss_phy.item() * B

        # approximate number of active neurons (h > threshold)
        active_count = (h > 0.01).float().sum(dim=1).mean().item()
        total_active += active_count * B

        if batch_count % PRINT_EVERY == 0:
            print(
                f"Epoch {epoch+1} | Batch {batch_count} | "
                f"Loss={loss.item():.4f} | DNA_CE={loss_dna.item():.4f} | "
                f"Phy_MSE={loss_phy.item():.5f} | Active={active_count:.1f}"
            )

    # Epoch summary
    N = SAMPLES_PER_EPOCH  # effective number of samples this epoch
    avg_loss = total_loss / N
    avg_dna  = total_dna / N
    avg_phy  = total_phy / N
    avg_active = total_active / N

    print(f"\n=== Epoch {epoch+1}/{num_epochs} COMPLETE ===")
    print(
        f"Avg Loss={avg_loss:.4f} | Avg DNA_CE={avg_dna:.4f} | "
        f"Avg Phy_MSE={avg_phy:.5f} | "
        f"Avg Active Neurons={avg_active:.1f} / {LATENT_DIM} "
        f"({100.0 * avg_active / LATENT_DIM:.1f}%)"
    )

    # Save checkpoint
    ckpt_path = f"sparse_ae_50bp_epoch{epoch+1}.pt"
    torch.save(model.state_dict(), ckpt_path)
    print(f"Saved checkpoint to {ckpt_path}\n")