We are building open-source tools that help rare-disease researchers reach answers faster. We start with fibrous dysplasia (FD/MAS), but the architecture is universal.
Research Canvas is an iterative AI–researcher collaboration platform - not an autonomous "AI scientist", not an ELN/LIMS, not yet another workflow builder for developers. AI proposes workflow variants and hypotheses; the researcher decides, modifies, clones; wet-lab results feed back into the AI. It is controlled autonomy: full AI freedom inside a block, deterministic skeleton between blocks, auditable trace of every run.
Agentic workflows for researchers: deterministic steps + AI blocks + a knowledge base (Karpathy-style wiki). The researcher defines the pipeline; the system executes it step by step with full control over each stage.
First use case: drug target prioritization for FD - ranking ~1000 molecular candidates down to the 5 most promising, with provenance for every score.
CLI MVP: June 2026
License: open-source (Apache 2.0)
AI monitors PubMed and drafts clinical-guideline updates. A clinician approves changes in a git-style PR review - every change is versioned and auditable.
Instead of a static PDF every few years - continuously updated, version-controlled clinical knowledge. Currently a post-MVP concept.
CRISPR / targeted editing - blocking the mutation in affected somatic cells.
Molecules blocking aberrant signaling - a preclinical direction with documented efficacy in mouse FD models. The path to clinical translation in humans.
Organoids / iPSC-derived models - tissue models for testing therapies in vitro.
Natural mechanisms - studying cases of spontaneous regression and natural protective mechanisms.
The plan has six parallel streams. Some are done, some are in progress, some are upcoming. We update this timeline live - no glossing over, with a concrete status on each item.
This roadmap is ambitious and may slip - especially milestones tied to the grant decision. We update each item's status on this page. If a specific stream interests you (CLI MVP, Live Guidelines, Patient Registry), get in touch - we'll happily share details and current progress.
After reviewing 13 AI-for-science platforms (Stanford Biomni, FutureHouse Kosmos, Google AI co-scientist, MIT ScienceClaw, HKU AI-Researcher, Benchling, and others) we identified a gap that nobody fills this way:
GeneQuest doesn't start from zero. The founder has 30 years of experience building enterprise systems, including commercial products deployed in large organizations.
A no-code tool automating work in BMC Helix ITSM / Remedy. Acquired by IBM, deployed at Telstra (savings on the order of 30 FTEs). Used in many countries, maintained for years.
A current portfolio product. A tool supporting ticket management in ITSM environments.
The same skills - building tools that solve real problems in large organizations - are now directed at rare diseases. Research Canvas and Live Guidelines aren't academic prototypes; they are products built by someone who knows how to ship software.
The first open release of Research Canvas is planned for June 2026. Leave your email - we will write when the repo goes public. Occasionally we will share progress in the meantime. No spam, no data trading.