Medical Genomics
Whole Exome Sequencing (Somatic)
19,433 genes, 300X Coverage, 18-20Gb Data, Clinical Report.
₹28,500per sample
TAT: 3 weeks
- Clinical-grade reporting
- High-coverage target regions
- Actionable genetic insights
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About this service
Detailed description for Whole Exome Sequencing (Somatic). This service includes comprehensive analysis and a detailed report delivered to you securely.
Service Workflow
- 1Sample CollectionPeripheral blood or tissue block collected and transported securely.
- 2Target EnrichmentSpecific capture of coding regions or disease-associated panel genes.
- 3High-Depth SequencingUltra-deep coverage sequencing on the Illumina NovaSeq X Plus.
- 4Variant CallingDetection of SNVs, indels, and CNVs with thorough clinical interpretation.
Frequently asked questions
What are the specimen requirements?
For most panels, we require peripheral blood in EDTA tubes (5ml volume). FFPE blocks are required for somatic panels.
Are the reports clinically actionable?
Yes, our bioinformatics pipeline generates comprehensive clinical reports detailing relevant pathogenic variants.
