Genome-Wide Sequencing: A Key to Genetic Insights
Genome-Wide Sequencing is a method used to study an organism’s complete DNA sequence. This process involves decoding the entire genome, which includes all the genetic material found in a living being’s chromosomes. Human genomes, for instance, contain about 3 billion base pairs of DNA. By sequencing the entire genome, scientists can uncover valuable information about genes, genetic variations, and potential mutations.
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