About This Service
Next Generation Sequencing
Our bioinformatics pipelines and tools facilitate precise detection of single nucleotide polymorphisms (SNPs), insertions and deletions (indels), copy number variations (CNVs), and structural variants from whole genome sequencing, whole exome sequencing, and targeted panel data. We provide end-to-end NGS analysis from raw FASTQ files to annotated variant calls with clinical-grade quality metrics.
Key Features
Our Process
Data Reception
We receive your raw sequencing data and assess quality.
Pipeline Execution
Automated analysis with best-practice bioinformatics tools.
Quality Control
Multi-level QC at every stage of the pipeline.
Reporting
Comprehensive reports with annotated variants and visualizations.
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Related Services
Consultation
Expert bioinformatics consultation for experimental design and analysis strategy.
Scientific Reporting
Publication-ready figures, manuscript writing, and grant application support.