Expert bioinformatics consulting and data analysis for academic labs, biotech, and pharma.
We analyze WGS/WES data, perform variant annotation and prioritization, and develop custom bioinformatics pipelines, databases, and analytical models to support genomic research and discovery.
Open to collaborations, consulting projects, and long-term research partnerships.
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PhD-level expertise in molecular biology, computational genomics, protein biochemistry, structural biology, and bioinformatics pipeline development.
We help analyze WGS/WES data to identify rare variants. Includes filtering, population frequency assessment, and functional impact prediction—research-ready insights without diagnostic interpretation.
We provide custom variant annotation integrating multiple databases, gene prioritization, functional impact prediction, and research reporting. Includes publication-ready figures, tables, and prioritized variant summaries for academic and biotech projects.
We can help you design custom bioinformatics workflows, optimize pipelines, and build and adapt databases for large cohorts—ensuring reproducible, automated, and efficient analysis.
Integrate genomic variants with protein structure and function. Includes variant mapping, cryo-EM dataset analysis, protein stability assessment, and mechanistic interpretation for research and biotech applications.
One-on-one coaching and group training in bioinformatics, variant analysis, and computational genomics, supporting students, researchers, and teams in enhancing analytical skills and workflow organization.
Assistance with data analysis for grants, co-authorship, and manuscript preparation. Includes visualizations and result interpretation.
From initial consultation to final deliverables. Payment is made after each milestone is completed and delivered as agreed.
Free consultation or email discussion to review your research objectives and define project scope. No obligation.
Detailed proposal with timeline, deliverables, and fixed price or hourly estimate.
Secure data transfer, analysis, and regular progress updates.
Results, interpretation, and revision rounds included.
No long-term commitments. Pay only for what you need — hourly, per project, or retainer.
Perfect for ad-hoc questions, quick analyses, or troubleshooting.
Custom quotes based on scope, samples, and complexity.
Dedicated support with priority access and discounted hourly rate.
Tailored databases and analysis designed for your cohort, study, or research project. From population-specific frequency curation to machine learning-based variant scoring, we deliver ready-to-use databases in any format your pipeline requires — VCF, JSON, TSV, Parquet, BigWig, SQLite, and more.
Custom datasets integrating multiple sources:
Advanced computational scoring for pathogenicity prediction:
Contextualize variants with functional genomics:
Not sure what you need? Schedule a free consultation to discuss your specific requirements.
Schedule a free 30-minute consultation to discuss your project.