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Lunit SCOPE GP

by Lunit@lunit_aiSeoul, Republic of KoreaNo ratings yet

AI genotype prediction from H&E pathology slides for research use

Visit lunit.io
Tool type
AI digital pathology genotype prediction software
Made for
Biopharma and translational research teams
Runs on
Digital pathology platforms with compatible scanners
Page describes compatibility with broad scanner and file types and deployment across digital pathology platforms and CRO partners; specific runtime environment not detailed.
Last checked
29 Oct 2026
3 product sources

What it does

Lunit SCOPE GP takes a single hematoxylin and eosin (H&E) tumor slide as input and predicts actionable tumor characteristics, including gene mutations such as EGFR and KRAS G12C and target protein expression. Its outputs include a genotype prediction probability score and a visualization of the predicted genotype area. Users can choose between high-sensitivity and high-specificity models for rule-out or rule-in testing.

Research teams use it to build customized pre-screening tools, screen for co-mutations from one slide, and generate AI-derived genomic signatures such as a TGFβ signature for biomarker and resistance discovery. It runs on Lunit's data-efficient foundation model, which is described as enabling faster development of new prediction models with reduced data requirements. A co-development with AstraZeneca for NSCLC driver mutation screening is described.

The product is aimed at biopharma and translational research teams and is labeled for Research Use Only, not for diagnostic procedures or decisions. A demo is requested through the Schedule a Demo link. Buyers should confirm commercial terms, supported scanners and file types, and detailed validation results directly with Lunit.

What it can do

  • Predicts gene mutations such as EGFR and KRAS G12C from a single H&E slide
  • Predicts target protein expression from H&E slides
  • Outputs a genotype prediction probability score
  • Visualizes the predicted genotype area on the slide
  • Supports high-sensitivity or high-specificity custom pre-screening models
  • Generates AI-derived genomic signatures such as TGFβ for biomarker discovery

Before you choose

  • Research Use Only; the page states it is not for use in diagnostic procedures or decisions.
  • No public pricing or plan details are listed; cost must be confirmed directly with Lunit.
  • Detailed validation results are not on the page and require contacting Lunit representatives.

Listed under

Get started

Start by requesting a demo from Lunit.

  1. Request a demo through the Schedule a Demo link on the SCOPE GP page.
  2. Confirm your H&E slide scanner and file type compatibility with Lunit's team, since the page cites broad scanner and file type support.
  3. Define whether you need a high-sensitivity or high-specificity model for your pre-screening or rule-in/rule-out use case.
Schedule a demo

Plans and prices

Cost basis, licensing model and any trial terms must be confirmed with Lunit through the demo request.

We couldn’t find published prices for Lunit SCOPE GP.

Sources for this overview

Product pages, documentation, and pricing checked 29 Oct 2026. Each source supports part of the overview; availability and prices can change.

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Last checked 29 Oct 2026. Every field keeps its source and date; unknown means we couldn’t confirm it.