About
Tools between medicine, genomics and software.
PJ Labs develops native apps at the intersection of medical research, bioinformatics and software design. The focus is on tools for informed users: people who analyse their own raw data, want to understand their annotations, or work scientifically and value a calm, precise interface.
The first product is Genome: a macOS workbench for local genome-data analysis. Genome wraps samtools, bcftools, bwa, fastp and minimap2 in a native SwiftUI interface, with integrated HLA typing (HLA*LA, T1K), KIR, pharmacogenetics (Aldy), repeat expansion (ExpansionHunter), Lp(a) KIV-2 (KILDA), microarray extraction, haplogroup analysis and PDF reports in one window, without cloud and without an account.
The approach: software that does one thing well instead of everything halfway. Every feature stands on peer-reviewed evidence, not on marketing metrics.
What PJ Labs stands for
- Scientific substance
- Every feature is based on peer-reviewed evidence. Method and primary source are referenced in the report, traceable, not just formatted.
- Data ownership
- Processing entirely local on the Mac. No account, no telemetry, no cloud uploads. Genomic raw data never leaves the device.
- Focused tools
- One app that fully solves a workflow, rather than a platform that covers many superficially. The feature scope is determined by the domain, not by market breadth.
- Native, not hybrid
- SwiftUI on Apple Silicon. No webview, no Electron shell. Platform primitives are used, not worked around.
Contact
Questions, feedback, collaborations.
Write directly to info@pjlabs.dev. No forms, no support tickets. Usually a reply within a few days.
Send email