Expert Consulting

Accelerate your
genomic research

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.

Email us at or schedule a free consultation to discuss your needs.

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30-minute videocall · No obligation · Pick a time that works for you

What We Can Help With

Biochemistry & Genomics Expertise

PhD-level expertise in molecular biology, computational genomics, protein biochemistry, structural biology, and bioinformatics pipeline development.

Rare Variant Discovery

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.

VCF Analysis & Annotation

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.

Pipeline and database Development

We can help you design custom bioinformatics workflows, optimize pipelines, and build and adapt databases for large cohorts—ensuring reproducible, automated, and efficient analysis.

Functional Genomics & Structural Biology

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.

Training & Mentorship

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.

Grant & Manuscript Support

Assistance with data analysis for grants, co-authorship, and manuscript preparation. Includes visualizations and result interpretation.

How It Works

Simple, transparent process

From initial consultation to final deliverables. Payment is made after each milestone is completed and delivered as agreed.

1
📞

Feasibility Call

Free consultation or email discussion to review your research objectives and define project scope. No obligation.

2
📋

Scope & Quote

Detailed proposal with timeline, deliverables, and fixed price or hourly estimate.

3
⚙️

Analysis

Secure data transfer, analysis, and regular progress updates.

4
📊

Delivery & Review

Results, interpretation, and revision rounds included.

Flexible Pricing

Choose what works for you

No long-term commitments. Pay only for what you need — hourly, per project, or retainer.

🎓 Academic discounts available. All rates are indicative only; personalized quotes will be provided based on specific needs and complexity.
Flexible

Hourly Consulting

$ 80 /hour

Perfect for ad-hoc questions, quick analyses, or troubleshooting.

  • 30-minute minimum
  • 24-48 hour response
  • Video call support
  • Pay as you go
Ideal for: Quick questions, method advice, interpretation help
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Best Value

Monthly Retainer

$ 350 +/month

Dedicated support with priority access and discounted hourly rate.

  • Starting at 5 hours/month (scalable)
  • Discounted overage rate
  • < 24h response
  • Monthly strategy call
Ideal for: Ongoing research, active projects, regular support needs
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Advanced Capabilities

Custom Genomic Databases & Analysis

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.

🧬

Frequency & Variant Databases

Custom datasets integrating multiple sources:

  • gnomAD, ClinVar, dbSNP with AC/AN from JSON
  • COSMIC integration (requires license)
  • Population-specific allele frequencies and constraints
  • Hardy-Weinberg equilibrium & quality filters

Machine Learning & Variant Scoring

Advanced computational scoring for pathogenicity prediction:

  • Train ML models on known benign and pathogenic variants
  • Threshold optimization for missense and loss-of-function variants
  • Aggregators of missense predictors (REVEL, SIFT, AlphaMissense, etc.)
  • Ensemble scoring at the variant level, adjusted by gene and disease context
📊

Functional Data Integration

Contextualize variants with functional genomics:

  • Tissue-specific expression (GTEx)
  • Protein domain annotations
  • Regulatory region mapping and variant impact scoring
  • Gene constraint, depletion, and disease relevance metrics
  • Structural biology integration using protein structures (PDB, AlphaFold) and cryo-EM data to assess variant impact in 3D context

Not sure what you need? Schedule a free consultation to discuss your specific requirements.

Ready to accelerate your research?

Schedule a free 30-minute consultation to discuss your project.

or reach out directly: to discuss your needs