Common Mutation Analysis by sanger/WGS.
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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.
Note : Our custom
analysis will provide valid solutions
and guarantee a high-quality report for
your research. Kindly share the
technical details of work for quotation
and lead time.
+ 91 9891 179928
info@allelelifesciences.com