Sanger sequencing, also known as chain-termination sequencing, is a method for determining the nucleotide sequence of DNA. It involves synthesizing a new DNA strand complementary to the template strand, but incorporating modified nucleotides (dideoxynucleotides) that terminate DNA synthesis. These terminated fragments are then separated by size, allowing the sequence to be read. It is commonly used for confirming DNA sequences, sequencing individual genes or small genomes, and for mutation detection.
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