Modifications of Kompetitive Allele-Specific PCR (KASP) Genotyping for Detection of Rare Alleles

Methods Mol Biol. 2023:2638:173-189. doi: 10.1007/978-1-0716-3024-2_12.

Abstract

KASP is commonly used to genotype bi-allelic SNPs and In/Dels, and the standard protocol works well when both alleles are nearly equally prevalent in the DNA template. To detect rare alleles in bulked samples or to distinguish more than three genotypes, such as tri-allelic loci or mutations across orthologous genes in polyploids, adjustments to the protocol and/or data analysis are required. In this chapter, we present modified protocols for these non-traditional applications, including reaction conditions that enhance the fluorophore signal from rare alleles, resulting in increased KASP assay sensitivity. We also describe alternative KASP data analysis approaches that increase statistical certainty of genotyping calls. Furthermore, this increased assay sensitivity enables high-throughput genotyping using KASP, as samples can be pooled and tested in a single reaction. For example, rare alleles can be detected in mixed seed pools when present in ratios as low as 1 in 200. The assay modifications presented here expand the options available for complex genotyping, and retain KASP's advantages of being cheap, fast, and accurate.

Keywords: Data transformation; FRET cassette; Genotyping; In/Del; KASP; Pooled DNA; Primer ratios; Rare alleles; SNP; Species identification.

MeSH terms

  • Alleles
  • Genotype
  • Humans
  • Nucleic Acid Amplification Techniques*
  • Polymerase Chain Reaction / methods
  • Polymorphism, Single Nucleotide
  • Polyploidy*