Why is Sanger Sequencing Important in Studying Genetic Mutations?
Sanger sequencing has been pivotal in identifying and characterizing genetic mutations. Its high accuracy makes it an ideal method for detecting point mutations, insertions, deletions, and other small-scale genetic changes. By providing a precise nucleotide sequence, researchers can pinpoint the exact location and nature of a mutation, which is crucial for understanding the genetic basis of diseases and for developing targeted therapies.
