Whole Exome Sequencing (WES)
Whole-exome sequencing is a widely used next-generation sequencing (NGS) method that involves sequencing the protein-coding regions of the genome.
Features of our test
- Single nucleotide variants (SNVs)
- Insertions and deletions (Indels)
- Structural variants (SVs)
- Copy number variants (CNVs)
- Repeat expansions
- Mitochondrial DNA (mtDNA) variants
- Paralogs
Sample Requirement
- Blood
- Swabs
- FFPE Tissue
- DNA Samples
Advance detection of almost all variants in a single test and analysis of:
- Copy Number Variants (CNVs)
- Greater lInsertions-Deletions (Indels)
- Single Nucleotide Polymorphisms (SNPs)
- Germline Variants
- Loss of Heterozygosity (LOH)
- Somatic Variants
Workflow: