About Us

We provide end-to-end computational solutions for complex genomic challenges, specializing in high-precision pipeline development and advanced algorithm design. With a focus on CRISPR safety and Next-Generation Sequencing (NGS), we help biotech startups and research labs transform raw sequencing data into validated, publication-ready insights.

Core Technical Expertise

Custom Pipeline Development

Scalable, reproducible workflows built with Nextflow and Snakemake, with full support for all major sequencing platforms:

  • Illumina — High-throughput short-read analysis
  • Oxford Nanopore & PacBio — Long-read assembly and structural variant detection

CRISPR & Gene Editing Analysis

Comprehensive on-target and off-target analysis, including PAM mismatch and chromatin structure integration.

  • Formalized risk assessments for therapeutic candidates

Advanced Sequencing Modalities

  • Single-Cell Sequencing (scRNA-seq) — Cell clustering, trajectory analysis, and differential expression
  • Ribosome Profiling (Ribo-seq) — High-resolution mapping of translation
  • RNA-seq — Transcriptome assembly and isoform quantification

Machine Learning & Custom Algorithms

  • Training and fine-tuning deep learning models (e.g., DeepVariant) for site-specific sequencing artifact recognition
  • Developing customized statistical algorithms to solve niche biological problems

Deliverables You Can Expect

Validated Codebases

Fully documented, containerized (Docker/Singularity) pipelines ready for production.

Technical Reports

Rigorous statistical summaries (Fisher's Exact, FDR corrections) for regulatory or internal review.

Performance Optimization

Refactoring existing legacy scripts for speed and cloud scalability.

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