Text Generation
Transformers
Safetensors
Upper Grand Valley Dani
llama
genomic
speculative-decoding
conversational
text-generation-inference
Instructions to use HuggingFaceBio/Carbon-500M with libraries, inference providers, notebooks, and local apps. Follow these links to get started.
- Libraries
- Transformers
How to use HuggingFaceBio/Carbon-500M with Transformers:
# Use a pipeline as a high-level helper from transformers import pipeline pipe = pipeline("text-generation", model="HuggingFaceBio/Carbon-500M") messages = [ {"role": "user", "content": "Who are you?"}, ] pipe(messages)# Load model directly from transformers import AutoTokenizer, AutoModelForCausalLM tokenizer = AutoTokenizer.from_pretrained("HuggingFaceBio/Carbon-500M") model = AutoModelForCausalLM.from_pretrained("HuggingFaceBio/Carbon-500M") messages = [ {"role": "user", "content": "Who are you?"}, ] inputs = tokenizer.apply_chat_template( messages, add_generation_prompt=True, tokenize=True, return_dict=True, return_tensors="pt", ).to(model.device) outputs = model.generate(**inputs, max_new_tokens=40) print(tokenizer.decode(outputs[0][inputs["input_ids"].shape[-1]:])) - Notebooks
- Google Colab
- Kaggle
- Local Apps
- vLLM
How to use HuggingFaceBio/Carbon-500M with vLLM:
Install from pip and serve model
# Install vLLM from pip: pip install vllm # Start the vLLM server: vllm serve "HuggingFaceBio/Carbon-500M" # Call the server using curl (OpenAI-compatible API): curl -X POST "http://localhost:8000/v1/chat/completions" \ -H "Content-Type: application/json" \ --data '{ "model": "HuggingFaceBio/Carbon-500M", "messages": [ { "role": "user", "content": "What is the capital of France?" } ] }'Use Docker
docker model run hf.co/HuggingFaceBio/Carbon-500M
- SGLang
How to use HuggingFaceBio/Carbon-500M with SGLang:
Install from pip and serve model
# Install SGLang from pip: pip install sglang # Start the SGLang server: python3 -m sglang.launch_server \ --model-path "HuggingFaceBio/Carbon-500M" \ --host 0.0.0.0 \ --port 30000 # Call the server using curl (OpenAI-compatible API): curl -X POST "http://localhost:30000/v1/chat/completions" \ -H "Content-Type: application/json" \ --data '{ "model": "HuggingFaceBio/Carbon-500M", "messages": [ { "role": "user", "content": "What is the capital of France?" } ] }'Use Docker images
docker run --gpus all \ --shm-size 32g \ -p 30000:30000 \ -v ~/.cache/huggingface:/root/.cache/huggingface \ --env "HF_TOKEN=<secret>" \ --ipc=host \ lmsysorg/sglang:latest \ python3 -m sglang.launch_server \ --model-path "HuggingFaceBio/Carbon-500M" \ --host 0.0.0.0 \ --port 30000 # Call the server using curl (OpenAI-compatible API): curl -X POST "http://localhost:30000/v1/chat/completions" \ -H "Content-Type: application/json" \ --data '{ "model": "HuggingFaceBio/Carbon-500M", "messages": [ { "role": "user", "content": "What is the capital of France?" } ] }' - Docker Model Runner
How to use HuggingFaceBio/Carbon-500M with Docker Model Runner:
docker model run hf.co/HuggingFaceBio/Carbon-500M
File size: 22,258 Bytes
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HybridDNATokenizer: Combines Qwen3 BPE tokenization with DNA 6-mer tokenization.
DNA sequences wrapped in <dna>...</dna> tags are tokenized as 6-mers.
All other text uses Qwen3's BPE tokenization.
Supports token_mask for Fine-grained Nucleotide Supervision (FNS):
-2: padding token
-1: text token (BPE)
0: DNA special token (<dna>, </dna>, <oov>)
1-5: partial 6-mer token — valid_length real bases at positions [0, valid_length),
right-padded with 'A' at positions [valid_length, k) so loss can supervise
positions 0..valid_len-1 via pos_mask = (valid_len > pos)
6: full 6-mer
"""
import os
import json
import warnings
import itertools
from typing import List, Optional, Tuple, Dict, Union, Any
from transformers import PreTrainedTokenizer, AutoTokenizer, BatchEncoding
class HybridDNATokenizer(PreTrainedTokenizer):
"""
Hybrid tokenizer combining Qwen3 BPE with DNA 6-mer tokenization.
DNA regions must be wrapped in <dna>...</dna> tags to be tokenized as 6-mers.
Without tags, DNA sequences are tokenized as regular BPE text.
For pure-DNA input (no metadata tokens), pass auto_dna_tags=True to have
<dna>...</dna> tags added automatically when they are absent. Do NOT set
this if the input may contain BPE metadata such as species tags
(<fungi_species> etc.) — those must appear outside <dna>...</dna> and would
be incorrectly k-mer encoded if auto-wrapping fired.
"""
model_input_names = ["input_ids", "attention_mask"]
def __init__(
self,
base_tokenizer_path: Optional[str] = None,
k: int = 6,
auto_dna_tags: bool = False,
**kwargs
):
self.k = k
# Load base tokenizer (Qwen3-4B-Base)
self._base_tokenizer = AutoTokenizer.from_pretrained("Qwen/Qwen3-4B-Base")
# Get base vocabulary
self._base_vocab = self._base_tokenizer.get_vocab()
self._base_vocab_size = len(self._base_vocab)
# Initialize DNA vocabulary
self._init_dna_vocab()
# Build combined vocabulary
self._build_combined_vocab()
# Set special tokens
self._eos_token = kwargs.pop('eos_token', None) or "<|endoftext|>"
self._pad_token = kwargs.pop('pad_token', None) or self._base_tokenizer.pad_token or "<|endoftext|>"
# Initialize parent class
super().__init__(
eos_token=self._eos_token,
pad_token=self._pad_token,
**kwargs
)
self.special_tokens = self.dna_special_tokens + [self._eos_token, self._pad_token]
self.auto_dna_tags = auto_dna_tags
def _init_dna_vocab(self):
"""Initialize DNA vocabulary (special tokens + k-mers + padding for 128 alignment)."""
bases = ['A', 'T', 'C', 'G']
# DNA special tokens
self.dna_special_tokens = ["<dna>", "</dna>", "<oov>"]
# Generate all k-mer combinations (4^k = 4096 for k=6)
self.kmers = [''.join(kmer) for kmer in itertools.product(bases, repeat=self.k)]
# DNA tokens start after base vocabulary
self.dna_start_id = self._base_vocab_size
# All DNA tokens get new IDs (no reuse of base vocab IDs, even for
# overlapping tokens like CCCCCC — they have different semantics in
# DNA context vs BPE context, per Qiuyi's recommendation)
base_dna_tokens = self.dna_special_tokens + self.kmers
# Calculate padding for 128 alignment
total_vocab_unpadded = self._base_vocab_size + len(base_dna_tokens)
target_vocab_size = ((total_vocab_unpadded + 127) // 128) * 128
num_padding_tokens = target_vocab_size - total_vocab_unpadded
# Add unused padding tokens
self.padding_tokens = [f"<unused_{i}>" for i in range(num_padding_tokens)]
# Create DNA token mappings — all get sequential new IDs
self.dna_token_to_id = {}
self.dna_id_to_token = {}
current_id = self.dna_start_id
for token in base_dna_tokens:
self.dna_token_to_id[token] = current_id
self.dna_id_to_token[current_id] = token
current_id += 1
# Add padding tokens
for token in self.padding_tokens:
self.dna_token_to_id[token] = current_id
self.dna_id_to_token[current_id] = token
current_id += 1
self.dna_vocab_size = len(base_dna_tokens) + len(self.padding_tokens)
# Set DNA special token IDs
self.dna_begin_token_id = self.dna_token_to_id["<dna>"]
self.dna_end_token_id = self.dna_token_to_id["</dna>"]
self.oov_token_id = self.dna_token_to_id["<oov>"]
def _build_combined_vocab(self):
"""Build combined vocabulary (base + DNA)."""
self._vocab = self._base_vocab.copy()
for token, token_id in self.dna_token_to_id.items():
if token not in self._vocab:
self._vocab[token] = token_id
self._id_to_token = {v: k for k, v in self._vocab.items()}
for token_id, token in self.dna_id_to_token.items():
if token_id not in self._id_to_token:
self._id_to_token[token_id] = token
@property
def vocab_size(self) -> int:
return max(self._vocab.values()) + 1
def get_vocab(self) -> Dict[str, int]:
return self._vocab.copy()
@property
def vocab(self) -> Dict[str, int]:
# Compatibility shim: fast tokenizers (PreTrainedTokenizerFast) expose
# `tokenizer.vocab` as a property; slow PreTrainedTokenizer subclasses
# like this one only expose `get_vocab()`. Some downstream tools
# (e.g. llama.cpp's convert_hf_to_gguf.py) read `.vocab` directly.
return self._vocab
def __len__(self):
# Override default (len(get_vocab())) because get_vocab() deduplicates
# CCCCCC which exists as both BPE (ID 91443) and DNA 6-mer (ID 154402).
return self.vocab_size
def _split_by_dna_tags(self, text: str) -> List[Tuple[str, bool]]:
segments = []
i = 0
n = len(text)
while i < n:
start_pos = text.find('<dna>', i)
end_pos = text.find('</dna>', i)
if start_pos == -1 and end_pos == -1:
remaining = text[i:]
if remaining:
segments.append((remaining, False))
break
if start_pos == -1 and end_pos != -1:
dna_region = text[i:end_pos + 6]
if dna_region:
segments.append((dna_region, True))
i = end_pos + 6
continue
if start_pos != -1 and end_pos == -1:
if i < start_pos:
normal_text = text[i:start_pos]
if normal_text:
segments.append((normal_text, False))
dna_region = text[start_pos:]
if dna_region:
segments.append((dna_region, True))
break
if start_pos < end_pos:
if i < start_pos:
normal_text = text[i:start_pos]
if normal_text:
segments.append((normal_text, False))
dna_region = text[start_pos:end_pos + 6]
if dna_region:
segments.append((dna_region, True))
i = end_pos + 6
else:
dna_region = text[i:end_pos + 6]
if dna_region:
segments.append((dna_region, True))
i = end_pos + 6
return segments
def _parse_dna_region(self, dna_region: str) -> Tuple[str, bool, bool]:
if dna_region == '<dna>':
return '', True, False
elif dna_region == '</dna>':
return '', False, True
has_start = dna_region.startswith('<dna>')
has_end = dna_region.endswith('</dna>')
content = dna_region
if has_start:
content = content[5:]
if has_end and content.endswith('</dna>'):
content = content[:-6]
return content.strip(), has_start, has_end
def _process_dna_sequence(self, dna_seq: str) -> Dict:
k = self.k
dna_seq = dna_seq.upper()
kmer_tokens = []
valid_bases = set('ATCG')
def is_valid_kmer(kmer):
return len(kmer) == k and all(base in valid_bases for base in kmer)
for i in range(0, len(dna_seq) - k + 1, k):
kmer = dna_seq[i:i+k]
if is_valid_kmer(kmer):
kmer_tokens.append(kmer)
else:
kmer_tokens.append("<oov>")
processed_length = len(kmer_tokens) * k
remaining = dna_seq[processed_length:]
padding_length = 0
valid_length = k
if remaining:
padding_needed = k - len(remaining)
# Right-pad with A: real bases occupy positions [0, valid_length).
# The hybrid BP loss supervises positions 0..valid_len-1 via
# pos_mask = (valid_len > pos)
# so padding must be at the END, not the start.
padded = remaining + 'A' * padding_needed
if is_valid_kmer(padded):
kmer_tokens.append(padded)
else:
kmer_tokens.append("<oov>")
padding_length = padding_needed
valid_length = len(remaining)
return {
"kmer_tokens": kmer_tokens,
"padding_length": padding_length,
"valid_length": valid_length,
}
def _tokenize(self, text: str, **kwargs) -> List[str]:
return list(text)
def _convert_token_to_id(self, token: str) -> int:
if token in self.dna_token_to_id:
return self.dna_token_to_id[token]
return self._base_vocab.get(token, self._base_tokenizer.unk_token_id or 0)
def _convert_id_to_token(self, index: int) -> str:
if index in self.dna_id_to_token:
return self.dna_id_to_token[index]
return self._id_to_token.get(index, "<oov>")
def convert_tokens_to_string(self, tokens: List[str]) -> str:
return "".join(tokens)
def encode(
self,
text: str,
add_special_tokens: bool = False,
return_token_mask: bool = False,
auto_dna_tags: Optional[bool] = None,
**kwargs
) -> Union[List[int], Tuple[List[int], List[int]]]:
use_auto = self.auto_dna_tags if auto_dna_tags is None else auto_dna_tags
if use_auto and '<dna>' not in text:
text = f'<dna>{text}</dna>'
segments = self._split_by_dna_tags(text)
token_ids = []
token_mask = [] if return_token_mask else None
for segment_content, is_dna in segments:
if is_dna:
dna_content, has_start, has_end = self._parse_dna_region(segment_content)
if has_start:
token_ids.append(self.dna_begin_token_id)
if return_token_mask:
token_mask.append(0)
if dna_content:
result = self._process_dna_sequence(dna_content)
for idx, kmer in enumerate(result["kmer_tokens"]):
token_id = self.dna_token_to_id.get(kmer, self.oov_token_id)
token_ids.append(token_id)
if return_token_mask:
if kmer == "<oov>":
token_mask.append(0)
elif idx == len(result["kmer_tokens"]) - 1 and result["padding_length"] > 0:
token_mask.append(result["valid_length"])
else:
token_mask.append(self.k)
if has_end:
token_ids.append(self.dna_end_token_id)
if return_token_mask:
token_mask.append(0)
else:
base_ids = self._base_tokenizer.encode(
segment_content,
add_special_tokens=add_special_tokens
)
token_ids.extend(base_ids)
if return_token_mask:
token_mask.extend([-1] * len(base_ids))
# Do NOT append EOS when add_special_tokens=True. Qwen3 doesn't add
# BOS/EOS either, and appending EOS here breaks lighteval's
# tok_encode_pair: it relies on
# len(encode(ctx)) + len(encode(answer)) == len(encode(ctx + answer))
# which the extra EOS violates by shifting the split by 1.
if return_token_mask:
return token_ids, token_mask
return token_ids
def decode(
self,
token_ids: Union[int, List[int]],
skip_special_tokens: bool = False,
**kwargs
) -> str:
if hasattr(token_ids, 'tolist'):
token_ids = token_ids.tolist()
if isinstance(token_ids, int):
token_ids = [token_ids]
if skip_special_tokens:
special_ids = {self.eos_token_id, self.pad_token_id}
token_ids = [tid for tid in token_ids if tid not in special_ids]
parts = []
i = 0
while i < len(token_ids):
tid = token_ids[i]
if tid == self.dna_begin_token_id:
dna_tokens = []
i += 1
while i < len(token_ids) and token_ids[i] != self.dna_end_token_id:
if token_ids[i] in self.dna_id_to_token:
dna_tokens.append(self.dna_id_to_token[token_ids[i]])
i += 1
dna_seq = ''.join(dna_tokens)
if skip_special_tokens:
parts.append(dna_seq)
else:
parts.append(f"<dna>{dna_seq}")
if i < len(token_ids) and token_ids[i] == self.dna_end_token_id:
parts.append("</dna>")
i += 1
elif tid in self.dna_id_to_token:
# This branch handles k-mer tokens that appear without a <dna>
# wrapper — the common generation case where <dna> was in the
# prompt but only the generated portion is being decoded.
# K-mer tokens are content, not special tokens, so always decode
# them. Only drop true DNA special tokens (<dna>, </dna>, <oov>)
# when skip_special_tokens=True.
is_dna_special = tid in (self.dna_begin_token_id, self.dna_end_token_id, self.oov_token_id)
if not (skip_special_tokens and is_dna_special):
parts.append(self.dna_id_to_token[tid])
i += 1
else:
text_ids = []
while i < len(token_ids):
curr_id = token_ids[i]
if curr_id in self.dna_id_to_token or curr_id == self.dna_begin_token_id:
break
text_ids.append(curr_id)
i += 1
if text_ids:
decoded = self._base_tokenizer.decode(text_ids, skip_special_tokens=skip_special_tokens)
parts.append(decoded)
return ''.join(parts)
def batch_decode(
self,
sequences: Union[List[int], List[List[int]], "torch.Tensor"],
skip_special_tokens: bool = False,
**kwargs
) -> List[str]:
return [
self.decode(
seq.tolist() if hasattr(seq, 'tolist') else list(seq),
skip_special_tokens=skip_special_tokens,
**kwargs
)
for seq in sequences
]
def __call__(
self,
text: Union[str, List[str]],
add_special_tokens: bool = False,
padding: bool = False,
truncation: bool = False,
max_length: Optional[int] = None,
return_tensors: Optional[str] = None,
return_token_mask: bool = False,
auto_dna_tags: Optional[bool] = None,
**kwargs
) -> Dict[str, Any]:
if add_special_tokens:
warnings.warn(
"HybridTokenizer does not support add_special_tokens=True, ignoring.",
UserWarning
)
add_special_tokens = False
is_batch = isinstance(text, list)
texts = text if is_batch else [text]
all_ids = []
all_masks = [] if return_token_mask else None
for t in texts:
if return_token_mask:
ids, mask = self.encode(t, add_special_tokens=add_special_tokens, return_token_mask=True, auto_dna_tags=auto_dna_tags)
all_ids.append(ids)
all_masks.append(mask)
else:
ids = self.encode(t, add_special_tokens=add_special_tokens, return_token_mask=False, auto_dna_tags=auto_dna_tags)
all_ids.append(ids)
if padding:
max_len = max(len(ids) for ids in all_ids)
if max_length:
max_len = min(max_len, max_length)
padded_ids = []
attention_masks = []
padded_token_masks = [] if return_token_mask else None
for idx, ids in enumerate(all_ids):
pad_len = max_len - len(ids)
if pad_len > 0:
ids = ids + [self.pad_token_id] * pad_len
attn = [1] * (max_len - pad_len) + [0] * pad_len
if return_token_mask:
mask = all_masks[idx] + [-2] * pad_len
else:
ids = ids[:max_len]
attn = [1] * max_len
if return_token_mask:
mask = all_masks[idx][:max_len]
padded_ids.append(ids)
attention_masks.append(attn)
if return_token_mask:
padded_token_masks.append(mask)
all_ids = padded_ids
all_masks = padded_token_masks
else:
attention_masks = [[1] * len(ids) for ids in all_ids]
result = {
"input_ids": all_ids if is_batch else all_ids[0],
"attention_mask": attention_masks if is_batch else attention_masks[0],
}
if return_token_mask:
result["token_mask"] = all_masks if is_batch else all_masks[0]
if return_tensors == "pt":
import torch
if is_batch:
result["input_ids"] = torch.tensor(result["input_ids"])
result["attention_mask"] = torch.tensor(result["attention_mask"])
if return_token_mask:
result["token_mask"] = torch.tensor(result["token_mask"])
else:
result["input_ids"] = torch.tensor([result["input_ids"]])
result["attention_mask"] = torch.tensor([result["attention_mask"]])
if return_token_mask:
result["token_mask"] = torch.tensor([result["token_mask"]])
return BatchEncoding(result, tensor_type=return_tensors)
def save_vocabulary(self, save_directory: str, filename_prefix: Optional[str] = None) -> Tuple[str]:
vocab_file = os.path.join(
save_directory,
(filename_prefix + "-" if filename_prefix else "") + "vocab.json"
)
with open(vocab_file, "w", encoding="utf-8") as f:
json.dump(self._vocab, f, ensure_ascii=False, indent=2)
return (vocab_file,)
def save_pretrained(self, save_directory: str, **kwargs):
os.makedirs(save_directory, exist_ok=True)
# Save base tokenizer files
self._base_tokenizer.save_pretrained(save_directory)
# Save DNA config
dna_config = {
"k": self.k,
"dna_start_id": self.dna_start_id,
"dna_vocab_size": self.dna_vocab_size,
"dna_special_tokens": self.dna_special_tokens,
"auto_dna_tags": self.auto_dna_tags,
}
dna_config_path = os.path.join(save_directory, "dna_config.json")
with open(dna_config_path, "w", encoding="utf-8") as f:
json.dump(dna_config, f, indent=2)
# Update tokenizer_config.json with auto_map
config_path = os.path.join(save_directory, "tokenizer_config.json")
if os.path.exists(config_path):
with open(config_path, "r") as f:
config = json.load(f)
else:
config = {}
config.update({
"tokenizer_class": "HybridDNATokenizer",
"auto_map": {
"AutoTokenizer": ["tokenizer.HybridDNATokenizer", None]
},
"k": self.k,
"auto_dna_tags": self.auto_dna_tags,
})
with open(config_path, "w", encoding="utf-8") as f:
json.dump(config, f, indent=2, ensure_ascii=False)
# Copy this tokenizer.py to save directory
import shutil
src_py = os.path.abspath(__file__)
dst_py = os.path.join(save_directory, "tokenizer.py")
if os.path.exists(src_py) and src_py != dst_py:
shutil.copy2(src_py, dst_py)
return (save_directory,)
@classmethod
def from_pretrained(cls, pretrained_model_name_or_path: str, **kwargs):
k = 6
auto_dna_tags = False
dna_config_path = os.path.join(pretrained_model_name_or_path, "dna_config.json")
tok_config_path = os.path.join(pretrained_model_name_or_path, "tokenizer_config.json")
if os.path.exists(dna_config_path):
with open(dna_config_path, "r") as f:
dna_config = json.load(f)
k = dna_config.get("k", 6)
auto_dna_tags = dna_config.get("auto_dna_tags", False)
elif os.path.exists(tok_config_path):
with open(tok_config_path, "r") as f:
tok_config = json.load(f)
k = tok_config.get("k", 6)
auto_dna_tags = tok_config.get("auto_dna_tags", False)
return cls(base_tokenizer_path=pretrained_model_name_or_path, k=k, auto_dna_tags=auto_dna_tags, **kwargs)
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