Genomics & Variant Analysis
Precision Genomics and Variant Analysis for Research and Beyond.
Whole Genome Sequencing (WGS) and Whole Exome Sequencing (WES)
Comprehensive analysis of an individual’s entire genome or exome to identify rare and common variants associated with diseases, traits, and ancestry.
Single-Cell Genomics
High-resolution analysis of genetic variation at the single-cell level, enabling insights into cellular heterogeneity, cancer evolution, and developmental biology.
Long-Read Sequencing (PacBio, Oxford Nanopore)
Advanced sequencing technologies that provide highly accurate, long-read data for resolving complex genomic regions, structural variants, and epigenetic modifications.
AI-Driven Variant Interpretation
Leveraging machine learning and artificial intelligence to prioritize clinically relevant variants, predict pathogenicity, and uncover novel disease associations.
Multi-Omics Integration
Combining genomics with transcriptomics, proteomics, and metabolomics data to provide a holistic view of biological systems and disease mechanisms.
Pharmacogenomics
Identifying genetic variants that influence drug response, enabling personalized medicine and optimizing therapeutic strategies.
CRISPR and Gene Editing Analysis
Supporting gene editing research with tools for off-target detection, editing efficiency quantification, and functional validation of edited variants.
Population Genomics
Large-scale genomic studies to uncover population-specific variants, evolutionary insights, and genetic determinants of complex traits.
Epigenomics and Methylation Analysis
Profiling DNA methylation and other epigenetic modifications to understand gene regulation, aging, and disease.
Rare Variant Discovery and Annotation
Advanced pipelines for detecting and annotating rare variants, including novel insertions, deletions, and structural variants.
Cancer Genomics
Tumor-normal paired sequencing to identify somatic mutations, copy number variations, and fusion genes driving cancer progression.
Microbiome Genomics
Analyzing host-microbiome interactions and microbial genomic variation to understand their role in health and disease.
Polygenic Risk Scoring (PRS)
Calculating personalized risk scores for complex diseases based on the cumulative effect of multiple genetic variants.
Real-Time Sequencing and Analysis
Offering rapid turnaround times for sequencing and analysis, particularly for infectious disease surveillance and outbreak tracking.
Genoma Bioinformatics 