Services · NGS Sequencing & Analysis
NGS Sequencing & Analysis
From sample intake to raw data analysis — NGS + full bioinformatics
Service description
Our NGS service has two parts: (1) Sequencing — we receive your sample, run library prep and next-generation sequencing on a standard platform; (2) Analysis — raw FASTQ data goes through a standard pipeline: QC, reference mapping, variant calling (SNP/InDel), annotation and prioritization. Already have data? We can handle analysis only.
What's included:- Sample intake & QC
- Library prep & sequencing
- Raw data QC (FASTQ)
- Reference genome mapping
- Variant calling SNP / InDel
- Annotation & prioritization
- Send sample or raw data
- Consultation on the right assay
- Run & data generation
- Full analysis & report
- Delivery: report + VCF/BAM
Deliverables
Complete analysis report + variant table + VCF/BAM + interpretation consult
Contact us to start
Send your project details and samples via the contact page or email — the first consultation is free.