genomic variations

What Techniques are Used to Identify Genomic Variations?

Several techniques are utilized to identify genomic variations. These include:
Whole Genome Sequencing (WGS): Provides a comprehensive overview of an individual's entire genome.
Whole Exome Sequencing (WES): Focuses on sequencing the coding regions of the genome, which are most likely to contain disease-causing mutations.
Chromosomal Microarray Analysis (CMA): Detects copy number variations that can cause developmental disorders.
Polymerase Chain Reaction (PCR): Amplifies specific DNA sequences to identify known mutations.

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