Request
Generate a canonical ATCG semantic trace, then explain what canonical means.
Maple Brain Lab · DNA Research
DOGMA and Hermon DNA are separate research programs. DOGMA asks whether regulated local computation can replace the transformer. Hermon DNA asks how far genome-native encoders can learn transferable biological sequence representations. Neither project claims AGI; both publish the evidence required to move toward it.
Start Here
A 509-page undergraduate guide connects molecular biology, DNA computing, machine learning, the canonical non-transformer DOGMA architecture, recursive evaluation, laboratories, and open research questions.
Measured DOGMA
Cycle 129Measured Hybrid Sample
This is a replay of a held-out evaluation, not simulated typing. The bootstrap compiler emits a canonical 64-base trace; a compact realization adapter produces the answer.
Generate a canonical ATCG semantic trace, then explain what canonical means.
Generate a canonical ATCG se
Canonical refers to a standardized, consistent sequence of A/T/C/G in DNA/RNA strands, ensuring uniformity in molecular structure and function. It defines expected patterns in genetic sequences, enabling accurate comparison and analysis across different biological contexts.
Non-transformer genomic computation network
Can intelligence emerge from regulated local structure, persistent state, and expression instead of self-attention?
DNA encoder and transformer research line
How far can genome-native representations support reliable sequence understanding and scientific reasoning?
The Boundary
DOGMA borrows organization principles such as local structure, regulation, persistent marks, transcription, and expression to define a new computational architecture. Its primary benchmark substrate can be text, code, symbolic sequences, or genomic data.
Hermon DNA models actual nucleotide sequences and scientific tasks. Its architecture is allowed to use transformers, bidirectional encoders, state-space models, and retrieval. The biology is in the data and evaluation target, not in a metaphor for the network.
Research Ladder
The phrase is a research direction, not a product claim. Progress means clearing increasingly difficult evidence gates while retaining prior capability, calibration, and diversity.
Learn compact sequence states that transfer across tasks and lengths.
Linear probes, retrieval, reverse-complement consistency, out-of-distribution transfer.Maintain and revise latent state under changing rules and delayed consequences.
Long-horizon recall, rule switches, counterfactual interventions, causal ablations.Build reusable programs from local operators, memory, and conditional expression.
Systematic generalization to unseen combinations and lengths.Turn diagnosed failures into better curricula or bounded architecture proposals.
Multi-cycle improvement against frozen suites without loss of diversity or prior skills.Form hypotheses, select experiments, and revise models under explicit resource and safety constraints.
Independent replication on new environments; no AGI claim before this evidence exists.Recursive Learning
Every cycle starts from measured failures, trains an isolated candidate, and ends at a frozen evaluation gate. Real-data anchors remain in the corpus; synthetic data is provenance-labeled and capped.
Primary Literature
These papers are references and baselines, not evidence that MapleAI has reproduced their results.
BPE tokenization, efficient multi-species pretraining, and the Genome Understanding Evaluation benchmark.
A family of DNA foundation encoders evaluated across human and multi-species genomic tasks.
Single-nucleotide, long-context genomic modeling using implicit convolutions instead of dense attention.
Bidirectional state-space modeling with reverse-complement equivariance for DNA.
Selective state-space sequence modeling with linear scaling in sequence length.
A long-context biological sequence model based on StripedHyena, spanning nucleotide to genome scales.