The Gimerny AI Platform

Five integrated products that cover the full drug discovery pipeline, from target identification through clinical trial optimization. Each product stands alone, all work better together.

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GimernyDiscover

AI-Driven Target Identification

GimernyDiscover transforms target identification from a years-long endeavor into a weeks-long process. By constructing massive biomedical knowledge graphs spanning protein-protein interactions, gene expression data, GWAS associations, and literature-mined relationships, Discover applies heterogeneous graph neural networks (HGNNs) to surface non-obvious target-disease connections. The platform integrates data from over 40 public and proprietary databases, cross-referencing genomic, transcriptomic, and proteomic signals to rank targets by druggability, novelty, and clinical translatability. Causal inference algorithms distinguish correlation from causation, while counterfactual reasoning modules predict the downstream effects of target modulation.

Core Technologies

Heterogeneous Graph Neural NetworksTransformer-based NLPCausal Inference (MR/IV)Neo4j Knowledge GraphsPyTorch Geometric
28,000+
Targets Evaluated
3 weeks
Avg. Time to Target
73%
Validation Hit Rate
2.1B
Knowledge Graph Edges

Key Capabilities

Biomedical Knowledge Graph

A proprietary graph with 2.1B edges spanning proteins, genes, diseases, pathways, and compounds, updated weekly from 40+ data sources.

Heterogeneous GNN Engine

Custom message-passing neural networks that reason across node and edge types, capturing complex biological semantics that homogeneous models miss.

Causal Inference Module

Mendelian randomization and instrumental variable analysis to distinguish causal targets from mere correlations in observational data.

Druggability Scoring

Multi-factor scoring that evaluates binding site geometry, pocket dynamics, selectivity risk, and competitive landscape for each candidate target.

Literature Intelligence

NLP models trained on 35M+ PubMed abstracts and full-text articles, extracting structured relationships and identifying emerging targets before they trend.

GimernyGenome

Multi-Omics Intelligence Platform

GimernyGenome is a multi-omics analysis platform that breaks down data silos between sequencing, expression, and functional assay data. Built on a biological foundation model pre-trained on 4.2 petabytes of sequencing data, Genome learns universal representations of biological entities that transfer across organisms, tissues, and disease contexts. The platform supports single-cell RNA-seq, bulk RNA-seq, whole-genome sequencing, proteomics (mass spec), and metabolomics data, providing unified embeddings that enable cross-modal queries. Differential expression analysis, pathway enrichment, and cell-type deconvolution run in minutes rather than days.

Core Technologies

Foundation Models (1.2B params)Contrastive Multi-Modal LearningSingle-Cell TransformersFederated LearningApache Arrow/Parquet
4.2 PB
Training Data
5
Supported Modalities
10M/run
Cell Processing
0.96
Variant Prediction AUC

Key Capabilities

Biological Foundation Model

A 1.2B parameter transformer pre-trained on 4.2PB of multi-species sequencing data, learning universal biological representations.

Cross-Modal Embeddings

Contrastive learning aligns representations across genomics, transcriptomics, proteomics, and metabolomics into a shared latent space.

Single-Cell Analysis

Process up to 10M cells per run with automated cell-type annotation, trajectory inference, and perturbation response prediction.

Variant Effect Prediction

Zero-shot prediction of variant pathogenicity using evolutionary and structural features, outperforming CADD and REVEL on ClinVar benchmarks.

Federated Analysis

Run analyses across institutional boundaries without moving raw patient data, maintaining HIPAA and GDPR compliance by design.

GimernyMolecule

Generative Molecular Design

GimernyMolecule is a generative chemistry platform that designs novel molecular structures optimized for potency, selectivity, ADMET properties, and synthetic accessibility simultaneously. Unlike traditional virtual screening, which searches existing chemical space, Molecule generates entirely new scaffolds by operating in 3D conformational space using equivariant diffusion models. The platform generates molecules conditioned on target binding pockets (structure-based) or known active compounds (ligand-based), with a multi-objective reinforcement learning loop that balances competing design criteria. Every generated molecule is scored against physics-based free energy calculations and ADMET predictors before being prioritized for synthesis.

Core Technologies

SE(3) Equivariant DiffusionProximal Policy OptimizationGNN-based DockingMM-GBSA Free EnergyRetrosynthetic Analysis
2.8M+
Molecules Generated
0.82
Avg. QED Score
94%
Synth. Feasibility
6 weeks
Hit-to-Lead Time

Key Capabilities

3D Equivariant Diffusion

SE(3)-equivariant diffusion models that generate molecules in 3D space, respecting rotational and translational symmetry of molecular interactions.

Multi-Objective RL

Proximal policy optimization balances potency, selectivity, solubility, metabolic stability, and synthetic accessibility in a single generation loop.

Structure-Based Design

Pocket-conditioned generation that fills binding sites with optimal interactions, guided by molecular docking and MM-GBSA rescoring.

ADMET Prediction Suite

21 ADMET endpoints predicted simultaneously, including CYP inhibition, hERG liability, plasma protein binding, and blood-brain barrier permeation.

Synthesizability Scoring

Retrosynthetic-aware scoring ensures every generated molecule can be made in 3-5 synthetic steps using commercially available reagents.

GimernySynth

AI-Powered Synthesis Planning

GimernySynth closes the gap between computational design and laboratory reality. The platform takes any target molecule, whether designed by GimernyMolecule or drawn manually, and produces ranked synthesis routes with step-by-step instructions, reagent lists, and yield predictions. The core engine is a transformer model trained on 15M+ published reactions from the USPTO, Reaxys, and proprietary reaction databases. Unlike rule-based retrosynthesis tools, Synth learns reaction patterns end-to-end, capturing subtle regio- and stereoselectivity preferences that hand-coded rules miss. A Monte Carlo tree search algorithm explores the retrosynthetic space, pruning routes that require unavailable reagents or hazardous conditions.

Core Technologies

Seq2Seq TransformersMonte Carlo Tree SearchGNN Yield PredictorsSupplier API IntegrationReaction Informatics
15M+
Reactions in Training Set
91.3%
Top-5 Accuracy
4.2
Avg. Route Steps
340K+
Routes Planned

Key Capabilities

Transformer Retrosynthesis

A sequence-to-sequence transformer trained on 15M+ reactions that proposes single-step disconnections with >90% top-5 accuracy.

Route Search (MCTS)

Monte Carlo tree search explores millions of possible routes, scoring by step count, yield, cost, and environmental impact.

Yield Prediction

Graph neural networks predict reaction yield with <8% MAE, accounting for solvent, temperature, catalyst, and substrate effects.

Reagent Availability

Real-time integration with supplier catalogs (Sigma-Aldrich, Enamine, ChemBridge) ensures every proposed route uses purchasable starting materials.

Hazard Assessment

Automated flagging of routes involving explosive, highly toxic, or environmentally hazardous intermediates, with safer alternatives suggested.

GimernyTrial

Clinical Trial Intelligence

GimernyTrial applies machine learning to the most expensive phase of drug development: clinical trials. The platform ingests historical trial data, electronic health records, and real-world evidence to optimize every aspect of trial design. Patient stratification models identify subpopulations most likely to respond, reducing required enrollment by 30-40%. Digital twin simulations run thousands of virtual trials to test protocol variations before a single patient is recruited. Adaptive trial designs powered by Bayesian optimization adjust dosing, endpoints, and enrollment criteria in real-time based on interim data.

Core Technologies

Bayesian Adaptive DesignDigital Twin ModelsCausal ML (DoWhy)Real-World Evidence MiningSurvival Analysis
35%
Enrollment Reduction
1.2M+
Trial Simulations Run
89%
Endpoint Accuracy
28%
Avg. Cost Savings

Key Capabilities

Patient Stratification

Multi-modal classifiers combine genomic, clinical, and imaging biomarkers to identify responder subpopulations with 85% precision.

Digital Twin Simulation

Patient-level digital twins trained on 2M+ historical patient records simulate treatment responses under varying protocol conditions.

Adaptive Trial Design

Bayesian optimization dynamically adjusts dosing, arm allocation, and interim analyses to maximize statistical power while minimizing patient exposure.

Endpoint Selection

Causal models evaluate surrogate endpoints against long-term outcomes, identifying endpoints that accelerate approval timelines.

Site Selection

Predictive models rank clinical sites by enrollment speed, data quality, patient diversity, and geographic accessibility.

See the Full Platform in Action

Schedule a personalized demo with our team to see how the Gimerny AI platform can accelerate your drug discovery pipeline.