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Targeted Panel Sequencing

Targeted gene sequencing panels are useful tools for analyzing specific mutations in a given sample.

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

Why do you need the targeted panel test?

To evaluate the genetic or hereditary threat advancement of overall survival through prior detection which eventually diminishes the cost of therapy and support the clinicians to decide on preventive measures.

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Covering nearly all kinds of disease areas including the rare ones using our latest next-generation sequencing technology.
Highest accuracy with exceptionally low error.

Covering the highest number of genes.
Cost-effective.

Covers disease-associated genes that are curated from the leading 5 databases

CCDS
Ensembl
ClinVar

RefSeq
GENCODE
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