Mutations Analysis Services

Mutation analysis is the process of finding variations in DNA sequences that could be connected to drug reactions, malignancies, or hereditary illnesses. Determining whether these mutations are acquired or inherited is essential for diagnosis, treatment, and prevention.

Research Area:

» Diagnose genetic diseases
» Identify cancer-driving mutations
» Precision Medicine plans
» Predict drug response
» Reproductive decisions and carrier screening
» Assess hereditary disease risk in families

Mutations are genetic changes acquired in germ cells or non-germ (somatic) cells. Mutations can be expressed as insertions, deletions, or base pair changes in coding or non-coding regions..

- ARMS-PCR
- Southern blot
- Next-Generation Sequencing (NGS)

Sanger Sequencing: The gold standard for identifying specific gene mutations, especially when a particular mutation is suspected.

Example Results

What a Mutation Analysis Result Looks Like

Note: A representative Sanger sequencing trace used for mutation confirmation. Your report includes your actual trace files and variant calls.