Window the sequence
Overlapping windows preserve coverage across long DNA inputs.
Read the sequence. Question the prediction.
Assess long DNA sequences without hiding gaps in coverage.
Window the input; keep predictions and evidence checks separate.
A research interface that reports coverage, output and unknown evidence explicitly.
Follow the connections as you scroll, or select a stage to see what happens there.
Overlapping windows preserve coverage across long DNA inputs.
A Transformer produces representations; window outputs converge into a sequence assessment.
Reference-linked evidence passes through explicit biological and automata-inspired checks.
Capstone research & engineering
AI / ML + Research + Backend
Research capstone · private source
A long DNA sequence rarely fits in a model’s input window. Truncating it hides what was never evaluated; a confident prediction without supporting evidence can hide even more.
Overlapping windows cover the submitted sequence. A custom k-mer Transformer produces window outputs that are aggregated into a sequence-level assessment. Reserved references supply query-linked evidence when a match exists; explicit constraints and a pushdown-automaton guardrail check that evidence separately.
The research interface reports coverage, model output and evidence status independently. An absent evidence match remains unknown. The portfolio illustrates this mechanism without publishing private code, data or model artifacts.
Windowing and aggregation make the evaluated portion of a sequence explicit instead of silently truncating the input.
Evidence retrieval and learned classification answer different questions. Missing reference evidence is never presented as proof of safety.
CKKS-related linear evaluation is an experimental branch. The main model prediction path remains plaintext; the diagram keeps those boundaries visible.