Innovative Science and Technology Solutions

Your sequencing data holds the answers. We build the systems to find them.

✅ Genomics Analysis & Variant Discovery

🧬 End-to-end genomics services — WGS, WES, and targeted sequencing with full variant discovery, SNP/indel analysis, structural variant detection, and genome annotation

🤖 AI/ML-powered insights — Cutting-edge pipelines that translate raw sequencing data into actionable intelligence for precision medicine, agriculture, and fundamental research

🎯 From raw data to real answers — Comprehensive interpretation of complex DNA datasets for researchers, clinicians, and biotech companies

Every cell tells a story. We build the systems to read it.

🔬 Comprehensive RNA analysis — Bulk RNA-seq, single-cell RNA-seq, and long-read transcriptomics covering differential expression, alternative splicing, pathway analysis, and regulatory network inference

🤖 AI-powered pattern discovery — Machine learning integrated directly into transcriptional analysis to uncover hidden biological signals across tissues, conditions, and time points

🧠 Robust biological interpretation — From raw expression data to clear, actionable insights that empower confident research decisions
 

The genome tells you what's possible. The proteome tells you what's actually happening.

🔬 Deep protein-level insights — Mass spectrometry-based quantitative & qualitative proteomics covering PTM analysis, protein-protein interaction mapping, and functional characterization

🔗 Integrative multi-omics — Combining proteomics with genomics and transcriptomics to reveal the full functional consequences of molecular changes at the protein level

💡 From expression to mechanism — Translating complex protein data into clear biological understanding of disease processes, drug targets, and therapeutic opportunities

Precise gene editing starts with precise computation — we make sure your cuts go exactly where they should.

✂️ Multi-platform gene editing support — Comprehensive computational analysis for CRISPR/Cas, TALEN, and other genome-editing technologies covering guide RNA design, editing outcome prediction, and on/off-target evaluation

🎯 AI-powered off-target prediction — Advanced NGS-based off-target nomination and validation using Digenome-seq, ONE-seq, and GUIDE-seq for maximum editing accuracy, efficiency, and safety

🔬 Integrative omics for editing optimization — Combining AI prediction models with multi-omics analysis to help researchers and biotech companies de-risk and optimize genome-editing programs

Your data already contains the answer. We build the AI to find it.

• 🤖 Robust predictive modeling — Building and validating AI/ML models (Random Forest, XGBoost, SVM, Deep Learning) that identify patterns and forecast biological behavior across complex multi-omics datasets
• 🔗 Multi-omics driven intelligence — Integrating genomics, transcriptomics, proteomics & metabolomics data into unified predictive frameworks for disease risk, biomarker discovery & therapeutic target nomination
• 🎯 From data patterns to biological answers — Turning noisy, high-dimensional biological datasets into reliable, interpretable predictions that drive real research and clinical decisions

Transformer models trained on your biology — not generic benchmarks.

• 🧠 Custom deep learning architectures — CNNs, RNNs, and Transformer-based models (BERT, DNA-BERT, Protein-BERT) purpose-built for DNA, RNA, protein sequence, and biological image analysis
• 🔍 Advanced feature extraction & generation — Autoencoders for dimensionality reduction, GANs and diffusion models for generative biology, and 3D structure prediction for functional modeling
• 🎯 Biology-first AI engineering — Deep learning solutions designed not just to model — but to reveal biologically meaningful patterns that drive real research and therapeutic breakthroughs