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Kai9987kai/supermix-expanse
supermix-expanse is a text generation model from Kai9987kai. Use it when you need the model to write or continue text. It is set up for pytorch. The card lists the license as other.
Supermix Expanse grafts, distils and fine-tunes five sources into one 132.6M-parameter PyTorch model:
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Updated Sep 24, 2026
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From the Hugging Face model README
Supermix Expanse grafts, distils and fine-tunes five sources into one 132.6M-parameter PyTorch model:
| Source | How it enters Expanse |
|---|---|
| Archimedes final (v93 trunk + v87 experts + FlyCore + Omni v48/v38) | the trunk everything is grafted onto; a frozen copy is the anti-forgetting teacher |
| Omni Collective v7 Frontier (77.6M) | frozen branch bridged into the residual stream + intent/domain distillation |
| Qwen2.5-Coder-7B-Instruct | 1,500 sandbox-verified code rows + 16 grafted MoE experts from its layer-0/1 MLP neurons |
| BioMedLM 2.7B | ~1,400 filtered biomedical rows + 16 grafted MoE experts from its layer-0/1 MLP neurons |
| Janelia male CNS v1.0 connectome (natverse/malecns, male-cns.janelia.org) | a per-token recurrent core wired as the whole male fly CNS at cell-type resolution + 6,000 connectome fact rows |
Status: experimental research model. Expanse keeps and improves Archimedes' own skills, but its new code and biomedical abilities are weak after one CPU training run (see Results). "Qwen3-Coder 7B/8B" was requested; Qwen has no Qwen3-Coder at that size, so the official Qwen2.5-Coder-7B-Instruct was used. BioMedLM replaced BioMistral-7B at the owner's request.
| file | what | recommended |
|---|---|---|
supermix_expanse_v3.pt | v1 re-tokenised with a byte-level BPE (8,864 tokens, no <unk>) and trained 5,000 more steps on ~42k rows incl. ~18k fresh verified problems, 5,150 verified Qwen code rows and 12k connectome facts | yes |
supermix_expanse.pt | v1: the original grafted + distilled model (word-level vocabulary) | baseline |
Compared on the same held-out rows (v1's dev split; loss per reply character, comparable across tokenizers) — full tables in compare_v1_v2_v3.md:
| v1 | v2 (not uploaded) | v3 | |
|---|---|---|---|
| replay (science / code tracing / arithmetic), nats/char | 0.166 | 0.132 | 0.033 |
| code, nats/char | 1.146 | 1.118 | 0.473 |
| male-CNS connectome (held-out cell types), nats/char | 0.181 | 0.176 | 0.124 |
| fly, nats/char | 0.393 | 0.369 | 0.314 |
| bio, nats/char (all rows) | 0.996 | 0.973 | 1.370 |
| fresh-number problems, exact answer (25) | 20% | 28% | 32% |
| connectome exact match / token-F1 (25) | 16% / 0.674 | 16% / 0.674 | 36% / 0.814 |
| biomedical token-F1 (25) | 0.285 | 0.343 | 0.220 |
| code pass rate, PubMedQA | 0% | 0% | 0% |
v3 is the strongest on replay, code loss, fly and connectome, and writes code in the right one-line shape, though not yet correctly enough to pass tests. It regressed on biomedical answers (connectome rows outnumber bio rows 5:1). v2 (native latent-consolidation blocks, code in code/expanse/src/consolidation_v2.py) was slightly better than v1 only because of extra training — zeroing its new blocks removes almost none of the gain — so it is not uploaded.
flowchart TD
P[Prompt] --> T[Word tokenizer + embeddings<br/>10,951 words, 320-d]
T --> L02[Trunk layers 0-2<br/>attention + MoE, 88 slots in L1-L2]
L02 --> G{{Graft site after layer 2<br/>each graft writes through a gate that starts at 0}}
G --> F[FlyCore<br/>22 fly brains, causal]
G --> O[Omni v48/v38<br/>prompt encoders]
G --> O7[Omni v7<br/>frozen 77.6M branch]
G --> C[Male CNS core<br/>11,751 cell types, 3.83M edges]
F & O & O7 & C --> L35[Trunk layers 3-5<br/>global attention + MoE]
L35 --> K[Thinking core + v93 CNS] --> N[Next word]
Male CNS core. Every token's layer-2 state drives the 1,277 sensory / visual / ascending cell types; activity runs 4 recurrent steps through all 3,830,931 type→type edges of the male CNS v1.0 (122.3M typed synapses), each edge weighted by its measured input fraction and signed by its presynaptic neurotransmitter (Dale's law); the 713 descending / motor / efferent types are read out, RMS-normalised and written back through a zero-initialised gate. Wiring and signs are fixed from the data; only per-type gain, bias and leak (plus in/out projections) are learned. It runs per position, so it is causal and KV-cache exact. |W| spectral radius 0.90.
Grafted experts. New MoE slots (72 → 88 in layers 1-2) hold 96-neuron experts carved from Qwen-Coder and BioMedLM layer-0/1 MLPs: ridge maps between single-token states of teacher and student, neuron selection by domain-weighted contribution, fold-in initialisation (SwiGLU for Qwen; GELU emulated exactly as silu(1.702z)/1.702 for BioMedLM), local function-fit refinement, load-matched wake biases, and 0.1× write strength for experts whose held-out fit is weak. They were born dormant and woken over 10-50% of training.
Honest graft numbers: the teacher→student representation maps are weak (held-out R² 0.05-0.15), and only 1 of 32 grafted experts reproduces its teacher neuron group on held-out tokens (Qwen layer 0, R² 0.21); the other 31 started at 0.1× write. Most of the transferred knowledge therefore comes from distillation, not from weights.
FlyCore.sense mean-pooled the hidden state over all positions (future tokens and padding included) and broadcast one write to every position; with the trained gate that leaks the future into every logit and makes KV-cached decoding differ from a full forward. Expanse senses per position.supermix_expanse_grafted.receipt.json).Dev loss per source (nats/token on reply tokens, held-out dev rows; connectome dev = held-out cell types):
| source | step 0 (= Archimedes + closed grafts) | final Expanse |
|---|---|---|
| Archimedes replay (science / code tracing / arithmetic) | 0.787 | 0.418 |
| Qwen code rows | 9.86 | 4.04 |
| BioMedLM bio rows | 8.25 | 4.95 |
| male-CNS connectome facts | 5.13 | 0.61 |
| fly rows | 4.62 | 1.20 |
Agreement with Omni v7: intent 72.7%, domain 73.1% (from 4% / 10%). Final gate magnitudes: CNS core 0.086, Omni v7 0.076.
Sample answers (greedy):
whats the impulse from 25 N acting for 4 s → impulse = force x time, 20 x 4 = 80, 5 x 4 = 20, the impulse is 100 newton seconds, total 100 ✅Python: r = sum(range(1, 6)) What is r? → range counts from 1 up to 5, … r is 15, total 15 ✅Which neurotransmitter does the cell type LC4 use in the male CNS? → answers a different connectome question (synapse count) ❌What is a hepatocyte? / Write a Python function that returns the sum of a list. → not usable ❌Held-out generation (greedy, 150 items per metric; full report eval_report.md):
| metric | Archimedes | Expanse |
|---|---|---|
| replay-style problems with freshly drawn numbers (exact answer) | 21.3% | 22.0% |
| code pass rate (sandbox tests) | 0% | 0% |
| biomedical token-F1 vs BioMedLM's answers | 0.088 | 0.313 |
| PubMedQA accuracy (always-yes baseline 60.5%) | 0% | 0% |
| connectome exact match (held-out cell types) | 0% | 17.3% |
| connectome token-F1 | 0.340 | 0.681 |
Ablations (Expanse dev loss with one component removed at inference):
| removed | replay | fly | code | connectome |
|---|---|---|---|---|
| nothing (Expanse) | 0.418 | 1.198 | 4.006 | 0.571 |
| male-CNS core gate → 0 | 0.447 | 1.233 | 4.088 | 0.596 |
| male-CNS core on the degree/sign-preserving rewired graph | 0.437 | 1.229 | 4.075 | 0.592 |
| Omni v7 gate → 0 | 0.429 | 1.217 | 4.025 | 0.583 |
| donor experts dead | 0.419 | 1.199 | 4.005 | 0.570 |
| FlyCore off | 0.419 | 1.198 | 4.006 | 0.571 |
The male-CNS core is the component the model relies on most, on every source including code, and a matched random graph loses 65-90% of its contribution — the trained model depends on the fly's specific wiring. Omni v7 helps slightly; the grafted donor experts and FlyCore contribute nothing measurable (the new knowledge came from distillation).
What is and is not shown. A gate opening shows training uses the connectome core; it does not show that the fly's wiring matters. The proper test is a matched training run on the degree/sign-preserving rewired graph (code included: connectome_full.rewired_graph) and a no-core control.
git clone https://huggingface.co/Kai9987kai/supermix-expanse
cd supermix-expanse/code/expanse
pip install torch sympy gradio
python expanse_chat.py --checkpoint ../../supermix_expanse_v3.pt # local chat UI (v3)
import sys, torch; sys.path.insert(0, "src") # from code/expanse
import expanse_core as ec
model, tok, payload = ec.load_expanse("../../supermix_expanse_v3.pt") # v3 (BPE) or v1 (word)
q = "whats the impulse from 40 N acting for 6 s"
ids, _ = tok.encode_turn(q, None)
out = ec.greedy_decode(model, torch.tensor([ids]), max_new_tokens=80,
omni_features=ec.arch.OmniCore.featurize([q]),
omni7_state=model.omni7_state_for([q]))
print(tok.decode(out))
The checkpoint is a pickled PyTorch payload (torch.load(weights_only=False)), not a Transformers model; load only if you trust it. Single-turn, 128-token context; v3 uses a byte-level BPE tokenizer, v1 a word-level vocabulary.
supermix_expanse_v3.pt — v3, recommended (schema supermix-expanse-v1 with a BPE tokenizer); supermix_expanse.pt — v1. Both self-contained (frozen Omni v7 net and connectome CSR buffers included)compare_v1_v2.md, compare_v1_v2_v3.md (+ .json) — same-row comparisons; supermix_expanse_v3*.receipt.json — v3 retokenisation and training receiptssupermix_expanse.receipt.json, supermix_expanse_grafted.receipt.json — training and build receipts (per-expert graft fits, vocabulary lift R², function-preservation check, full training history)code/expanse/ — build, train, eval, teacher-data, chat and connectome code (DESIGN.md is the spec); code/supermix-archimedes/ and code/external/omni_v7/ — the source it depends ondata/ — the teacher corpora actually used (code, cleaned bio, connectome facts), data/v3/ (fresh verified problems + connectome v3 rows), the unbiased PubMedQA eval set, and data receiptsComposite — see LICENSE.md. In short: code MIT (Kai Piper); the weights contain parameters derived from BioMedLM and were trained on its outputs, so the BigScience OpenRAIL-M use restrictions apply to this model and its derivatives — in particular it must not be used to provide medical advice or medical results interpretation; Qwen2.5-Coder-7B-Instruct is Apache-2.0; the male CNS connectome data (Janelia FlyEM and collaborators) is CC BY 4.0; PubMedQA is MIT.
malecns R package.