File size: 9,193 Bytes
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Written so the code runs unchanged on another machine. Nothing here hardcodes a lab path:
each model is named, and resolution walks an ordered search path
1. ``$VERA_MODEL_ROOT/<relative path>`` -- an explicit, machine-local root
2. any directory in ``$VERA_MODEL_PATH`` -- colon-separated, like ``$PATH``
3. the Hugging Face cache, via the hub id -- downloaded on first use
so a new machine needs at most one environment variable, and none at all if it is willing
to download. `ensure_local` reports which rung it used, because "the model was silently
re-downloaded" and "the model was silently the wrong one" are both failures that look like
success.
Layout under a root is fixed and shallow, so a directory can be rsynced between machines
and still resolve::
$VERA_MODEL_ROOT/
c2s/celltype/ vandijklab/C2S-Pythia-410m-cell-type-prediction
dna/nucleotide-transformer/ InstaDeepAI/nucleotide-transformer-v2-500m-multi-species
dna/dnabert2/ zhihan1996/DNABERT-2-117M
"""
from __future__ import annotations
import os
from dataclasses import dataclass
from pathlib import Path
# Where a lab machine may already hold these, tried before any download. Extend rather
# than edit: an unreachable entry is skipped, so listing several machines is harmless.
FALLBACK_ROOTS = (
Path("/srv/disk00/sshfs/pengchx3/vera_models"),
Path("/tmp/galaxy_srv_disk00/pengchx3/vera_models"),
)
# Tasks a model can answer. Grouping by task rather than by model is deliberate: rbio1
# reports that *composing* several approximate verifiers beats any one of them, and a
# registry keyed by model cannot express "ask everything that speaks to this question".
CELL_TYPE = "cell_type"
DNA_SEQUENCE = "dna_sequence"
@dataclass(frozen=True)
class ModelSpec:
"""One callable pretrained model.
Attributes:
key: Short name used by callers and on the command line.
hub_id: Hugging Face id, used for download and as the cache key. Empty for
models that are not distributed through the hub (see `kind`).
relpath: Location under a model root, so roots stay rsync-compatible.
task: Which question this answers. Several models may share a task.
kind: How to load it -- ``"hf"`` for transformers weights, ``"celltypist"`` for a
CellTypist model resolved by name. New kinds are added here rather than by
special-casing at call sites.
description: What it answers, in the vocabulary of the benchmark's questions.
tokenizer_hub_id: Where to get the tokenizer when the weights directory has
none. Several HF repos ship weights only and expect the base model's
tokenizer; loading `AutoTokenizer` from such a directory does not raise --
it yields a tokenizer that encodes to ZERO tokens, and generation then fails
with an unrelated reshape error minutes later.
note: Anything a caller must know before trusting its output.
"""
key: str
hub_id: str
relpath: str
task: str
description: str
kind: str = "hf"
tokenizer_hub_id: str = ""
note: str = ""
REGISTRY: dict[str, ModelSpec] = {
"c2s-celltype": ModelSpec(
key="c2s-celltype",
hub_id="vandijklab/C2S-Pythia-410m-cell-type-prediction",
relpath="c2s/celltype",
task=CELL_TYPE,
description="cell type from a cell's ranked gene expression (Cell2Sentence)",
# The published repo ships weights without a tokenizer; C2S-Pythia is a Pythia
# derivative, so the base tokenizer is the correct one.
tokenizer_hub_id="EleutherAI/pythia-410m",
note="Cell2Sentence: input is gene symbols ordered by descending expression.",
),
# A second, independent opinion on the same question. CellTypist is a different model
# family (regression over marker genes, not a language model), so its agreement with
# Cell2Sentence is evidence rather than a restatement -- two models that fail the same
# way would agree confidently and teach nothing.
"celltypist": ModelSpec(
key="celltypist",
hub_id="",
relpath="celltypist",
task=CELL_TYPE,
description="cell type from an expression matrix (CellTypist, marker-based)",
kind="celltypist",
note="Resolved by CellTypist model name, e.g. Immune_All_Low.pkl.",
),
"nt-500m": ModelSpec(
key="nt-500m",
hub_id="InstaDeepAI/nucleotide-transformer-v2-500m-multi-species",
relpath="dna/nucleotide-transformer",
task=DNA_SEQUENCE,
description="embed or score a DNA sequence (Nucleotide Transformer v2)",
),
"dnabert2": ModelSpec(
key="dnabert2",
hub_id="zhihan1996/DNABERT-2-117M",
relpath="dna/dnabert2",
task=DNA_SEQUENCE,
description="embed a DNA sequence (DNABERT-2)",
),
}
def models_for_task(task: str) -> tuple[ModelSpec, ...]:
"""Every registered model that answers `task`, in registration order.
Callers that want a consensus iterate this rather than naming one model, so adding a
model to the registry widens the consensus without touching call sites.
"""
return tuple(m for m in REGISTRY.values() if m.task == task)
def search_roots() -> list[Path]:
"""Model roots to try, most explicit first."""
roots: list[Path] = []
explicit = os.environ.get("VERA_MODEL_ROOT")
if explicit:
roots.append(Path(explicit).expanduser())
for entry in (os.environ.get("VERA_MODEL_PATH") or "").split(os.pathsep):
if entry.strip():
roots.append(Path(entry.strip()).expanduser())
roots.extend(FALLBACK_ROOTS)
return roots
def _looks_like_a_model(path: Path) -> bool:
"""Whether `path` holds loadable weights, not just an empty placeholder.
Checked because an interrupted copy leaves a directory that exists and fails at load
time, several minutes into a run. Weights only -- the tokenizer is resolved separately
by `resolve_tokenizer`, because some repos legitimately ship without one.
"""
if not path.is_dir():
return False
if not (path / "config.json").is_file():
return False
return any(path.glob("*.safetensors")) or any(path.glob("*.bin"))
TOKENIZER_FILES = ("tokenizer.json", "tokenizer_config.json", "vocab.json",
"spiece.model", "merges.txt")
def has_tokenizer(path: Path) -> bool:
"""Whether a directory carries a usable tokenizer.
Note the doubled `any`: ``any(path.glob(p) for p in ...)`` tests the truthiness of
generator OBJECTS, which are always truthy, so that spelling returns True for an
empty directory. This guard silently passed before it was mutation-tested.
"""
return any(any(path.glob(name)) for name in TOKENIZER_FILES)
def resolve_tokenizer(key: str) -> tuple[str, str]:
"""Resolve where to load this model's tokenizer from.
Returns:
``(target, source)`` as `resolve` does. Falls back to `tokenizer_hub_id`, then to
the model's own hub id, when the local weights directory has no tokenizer files.
"""
spec = REGISTRY[key]
local = find_local(key)
if local is not None and has_tokenizer(local):
return str(local), "local"
return (spec.tokenizer_hub_id or spec.hub_id), "hub"
def find_local(key: str) -> Path | None:
"""First local directory holding this model, or None.
Raises:
KeyError: If `key` is not registered, so a typo fails loudly rather than
silently falling through to a download of nothing.
"""
spec = REGISTRY[key]
for root in search_roots():
candidate = root / spec.relpath
if _looks_like_a_model(candidate):
return candidate
return None
def resolve(key: str) -> tuple[str, str]:
"""Resolve a model to something loadable.
Args:
key: Registry key.
Returns:
``(target, source)`` where `target` is a local path or a hub id, and `source` is
``"local"`` or ``"hub"``. Callers should log `source`: a silent fall-through to
the hub is how a 15 GB re-download happens on a machine that already had the file.
Raises:
KeyError: If `key` is not registered.
"""
spec = REGISTRY[key]
if spec.kind != "hf":
raise ValueError(f"{key!r} is a {spec.kind} model; resolve() is for hub weights")
local = find_local(key)
if local is not None:
return str(local), "local"
return spec.hub_id, "hub"
def describe() -> str:
"""One line per registered model, for a prompt or a CLI listing."""
lines = []
for task in sorted({m.task for m in REGISTRY.values()}):
lines.append(f"[{task}]")
for spec in models_for_task(task):
if spec.kind == "hf":
target, source = resolve(spec.key)
where = f"{source}: {target}"
else:
where = spec.kind
lines.append(f" {spec.key:<14} {spec.description} [{where}]")
return "\n".join(lines)
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