EasyCAPS: A web tool for restriction-based genotyping and rational CRISPR-Cas9 donor design
Tracking Single Nucleotide Polymorphisms (SNPs) following CRISPR-Cas9 genome editing is a critical yet often labor-intensive step in modern genetic research. Although Sanger sequencing is the conventional method for definitive confirmation, it typically requires substantial time to generate results. In contrast, PCR-based restriction methods like CAPS (Cleaved Amplified Polymorphic Sequence) and dCAPS (derived CAPS) offer rapid and cost-effective alternatives. However, existing dCAPS primer design tools suffer from significant limitations and were largely developed for tracking polymorphisms in plant genomes. Concurrently, CRISPR-Cas9 gene editing requires strategies to prevent the re-cleavage of the edited allele, typically involving the modification of the Protospacer Adjacent Motif (PAM). To address these challenges, we developed EasyCAPS, a web-based tool that integrates dCAPS primer design with advanced functionalities for CRISPR experiments. EasyCAPS overcomes the shortcomings of previous software by enabling restriction enzyme pre-selection and optimizing designs for complex DNA sequences. Its key innovation is the "Hiding PAM" feature, which designs synonymous mutations to mask the Cas9 recognition site while accounting for codon usage bias, thereby facilitating one-step allelic exchange. The utility of the tool was demonstrated through practical applications targeting the HTA1, PHO84, and CAT5 genes, significantly accelerating both genotyping and gene editing processes. We conclude that EasyCAPS is an accessible solution that effectively streamlines molecular biology workflows.