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DNA Sequencing, as it pertains to Biomarkers within Genetics and Mutation, refers to the process of determining the order of nucleotide bases – adenine, guanine, cytosine, and thymine – in a DNA molecule. This technique provides important information about specific genes or regions of DNA, enabling the identification of genetic variations, mutations, and other biomarkers that can be linked to diseases or other biological conditions. In this context, DNA Sequencing serves as an essential tool for understanding genetic factors contributing to various health issues and facilitates the development of targeted treatments and diagnostic tests. By deciphering the precise arrangement of nucleotides in a DNA sequence, researchers gain valuable insights into the genetic makeup of individuals, populations, or organisms, paving the way for advancements in personalized medicine, gene therapy, and evolutionary biology.