Every claim.Every source.Every time.
Helixor turns millions of PubMed Central articles into verified, traceable variant evidence — instantly.
Helixor Turns Millions OfPubMed Central Articles IntoVerified, Traceable VariantEvidence, Instantly.
01 / The Dig
You read the whole paper to find one number in Table S12.
02 / The Spreadsheet
You lost which row that snippet was from.
03 / The Notation
The search returned nothing.
The paper existed. It used a different notation.
c.5266dupC
04 / The Summary
None of this is negligence. It's the workflow.
Helixor was built to fix the workflow.
What is Helixor
We find the signal. You classify.
See it in action
Search. Filter. Trace to source.
Watch a real search against indexed PubMed Central articles.
Features
Built for the rigor curators demand
Multi-notation Search
HGVS coding, protein, rsID, legacy names — search all notation forms simultaneously. Never miss a paper because it used a different format.
Supplement & Table Mining
Tables and supplementary files surface first. The evidence curators need most is often the hardest to find — until now.
ACMG Evidence Mapping
Claims categorized by evidence type: PS3 functional, PP1 segregation, PM2 population frequency, and more.
Context-aware Results
Germline, somatic, mosaic — or "unknown" when the paper doesn't state it. Helixor never guesses.
Smart Alerts
Save a search. Get notified when new PubMed Central papers match your variant.
Filter by Evidence Type
Functional, segregation, frequency, case report — drill down to exactly what you need for classification.
Why Helixor
Built on trust, not promises.
Launching at InSight 2026
Singapore
Live demo with real curator workflows. Request early access below.
Built on PubMed Central
Full-text open access
The same trusted source curators already rely on — indexed, structured, and searchable.
100% traceable
No hallucinations
Every displayed claim links to an exact verbatim snippet. No paraphrases. No guesses.