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Identifying heterozygous base positions or small insertions or deletions in genomic DNA is often employed to locate mutations or polymorphisms in diploid organisms, detect genetic rearrangements, and uncover rare variants.
Sanger sequencing is the gold standard of sequencing technology: it provides high accuracy, long-read capabilities, and flexibility to support a diverse range of applications. Sanger sequencing is mostly known for DNA sequencing applications, but also supports applications in RNA sequencing and epigenetic analysis.
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