Research Driven.
Cloud Native Genomics.
Democratizing access to high-quality, reproducible, and production-ready sequencing analysis for researchers, clinicians, and biotech organizations. Our approach is practical, research-driven, and rooted in the challenges faced by working scientists.
Powering workflows with
Our Capabilities
Current Technical Initiatives
Production WES
A comprehensive variant calling workflow optimized for cancer genomics. Identifies clinically actionable mutations with precision.
- Somatic & Germline calling
- ACMG Classification
End-to-End NGS Pipeline Development
We engineer robust, scalable pipelines using Nextflow and Snakemake that are ready for clinical and research production. Our workflows are containerized (Docker/Singularity) and built with automated testing to ensure reproducibility across any infrastructure.
- ✓ Custom WGS, WES, and RNA-seq workflows
- ✓ nf-core best practices implementation
- ✓ Automated quality control & reporting
Translation & Variant Interpretation
Turn raw sequencing data into biological insights. We integrate advanced annotation frameworks and machine learning models to prioritize variants, identify biomarkers, and interpret complex genomic landscapes.
- ✓ Clinical variant prioritization (ACMG/AMP)
- ✓ Multi-omics data integration
- ✓ Custom annotation database creation
Cloud-Native Infrastructure
We design and deploy secure, cost-optimized cloud environments for bioinformatics. Whether on AWS, Azure, or Google Cloud, we ensure your data and compute scale efficiently to meet demand without breaking the bank.
- ✓ Serverless & Batch architecture design
- ✓ Spot instance optimization (up to 70% savings)
- ✓ Infrastructure as Code (Terraform/CDK)