From Complex Data to Actionable Discovery
Transforming genomic data into meaningful insights for academic, clinical, and pharmaceutical research. Accelerating discoveries that matter.
How We Simplify Bioinformatics
Our streamlined process ensures you get from data to discovery, faster and more efficiently than ever before.
Data Submission
Securely upload your raw data through our easy-to-use portal with automated validation.
Analysis & Interpretation
Our experts use proprietary pipelines and AI algorithms to analyze and interpret your data.
Actionable Reports
Receive comprehensive, publication-ready reports with clear insights and visualizations.
Our Bioinformatics Services
Comprehensive analysis solutions tailored to your research needs
Genomics
Whole genome, exome, and targeted sequencing analysis with advanced variant calling and annotation.
- Variant Discovery & Annotation
- Family-based Analysis
- CNV/SV Detection
Transcriptomics
RNA-Seq analysis for differential expression, pathway enrichment, and functional annotation.
- Differential Expression
- Pathway Analysis
- Alternative Splicing
Metagenomics
Microbial community profiling and functional analysis from 16S and shotgun sequencing data.
- Taxonomic Classification
- Functional Profiling
- Diversity Analysis
Epigenomics
Analysis of DNA methylation, histone modifications, and chromatin accessibility data.
- DNA Methylation Analysis
- ChIP-Seq Analysis
- ATAC-Seq Processing
Single-Cell Analysis
Single-cell RNA-Seq analysis for cellular heterogeneity and developmental trajectories.
- Cell Clustering
- Trajectory Inference
- Differential Expression
Custom Solutions
Tailored bioinformatics pipelines and analysis workflows for specific research questions.
- Pipeline Development
- Script Optimization
- Cloud Integration
Our Platform Suite
Proprietary platforms designed to accelerate your research workflow
GeneAssure Platform
Cloud-based NGS analysis platform
An integrated platform for streamlined NGS data analysis, visualization, and collaborative research management.
- Automated pipeline execution with version control
- Interactive visualization dashboard
- Team collaboration tools
- Secure data storage and sharing
RareVarDB
Curated rare variant database
A comprehensive database of clinically annotated rare genetic variants with population frequency data and pathogenicity predictions.
- Clinically annotated variants from global populations
- 20+ in-silico prediction scores
- Real-time updates from literature
- API access for integration
Our Impact in Numbers
Driving discoveries through data since 2020
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Research Institutions
Start Your Discovery Journey Today
Ready to transform your data into discoveries? Get in touch with our expert team.