Introduction to the READIT^® SNP Genotyping System: Applications 

The READIT^® System can be used to detect and/or distinguish a variety of sequences. Its specificity allows it to be used to detect SNPs, deletions, insertions and translocations. Assays can also be designed to detect the presence of a particular sequence or determine the allelic frequency in mixed samples.

This summary will necessarily cover only a very small number of applications. It will give you some idea of what the READIT^® System might do for you.