Whether you need a curated database, custom bioinformatics analysis, or a prioritized target report — we deliver research-grade intelligence built on experimentally validated data.
Every gene in our database is classified into a druggability tier based on experimental validation, published evidence, and existing drug availability.
Strong experimental evidence, high druggability, existing approved/pipeline drugs. Highest confidence for therapeutic intervention.
Solid evidence base, known druggable domains, repurposing opportunities identified from existing pharmacopoeia.
Emerging evidence, potential druggable features, requires additional validation but showing strong biological rationale.
Preliminary associations, early-stage evidence. Included for completeness and to support exploratory research programs.
Illustrative example — actual database contains 5,000+ entries
| Gene | Tier | Druggable | Repurposing | Indication |
|---|---|---|---|---|
| EGFR | Diamond | Yes | Erlotinib, Gefitinib | Lung Adeno. |
| KRAS | Diamond | Yes | Sotorasib | Pancreatic |
| TP53 | Gold | Limited | Under investigation | Colorectal |
| FGFR2 | Gold | Yes | Erdafitinib | H&N Carcinoma |
| CDK12 | Diamond | Yes | Dinaciclib | SCLC |
Five high-impact solid tumor types with curated gene sets. Expanding to additional cancer types and therapeutic areas.
1,000+ genes
1,000+ genes
1,000+ genes
1,000+ genes
1,000+ genes
End-to-end analysis from raw sequencing files to prioritized therapeutic targets — with human validation at every stage.
FASTQ files, BAM/CRAM, or raw sequencer output from your NGS platform
Quality control, adapter trimming, and reference genome alignment
Variant calling, differential expression, pathway enrichment
Cross-reference with our 5,000-gene database for druggability and tier classification
Prioritized target list, repurposing candidates, publication-ready report
Every gene validated against published literature and experimental data. No automated scraping, no unverified predictions.
Our team brings hands-on experience from GMP pharmaceutical R&D environments — we understand what drug development teams actually need.
From reagent supply to sequencing analysis to target prioritization — a single partner across your entire discovery workflow.
Our drug repurposing maps accelerate timelines by identifying existing approved molecules with evidence for new indications.
Whether you need database access, a bioinformatics pipeline, or a custom target report — let's discuss how we can support your research.