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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

Why should you choose us

  • Achieves uniform coverage of ≥90% and accurate detection and analysis.
  • Produces a shorter and better manageable data set for quicker and easier data analysis.

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