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A CAPS (cleaved amplified polymorphic sequence) marker was developed to detect the Ara h 1.02 truncation mutant in succeeding generations.
A CAPS screening cut-off score of ≥45 was used to dichotomize the population, as suggested in the literature [ 64].
A CAPS assay of nineteen individuals segregating for the presence of the candidate y11 SNP found that the SNP perfectly cosegregated with the foliage phenotype.
A CAPS marker was developed generating TaqI recognition fragments of 167 and 218 bp in cultivars with Hap-6A-A and Hap-6A-G, respectively.
A CAPS assay of seventeen individuals segregating for the presence of CD-5 showed prefect cosegregation of the candidate SNP with the mutant phenotype.
A CAPS marker was developed based on the -593 A/G polymorphism and association analysis indicated that Hap-6A-A increased TKW by more than 3.1 g [ 19].
A CAPS markers designed to the promoter VRN-1 region allowed us to reveal the three most frequent allelic variants in diploids, while avoiding a large scale sequencing approach.
A CAPS marker A3-0200), homologous to Bra038794 at 24.02 Mb, was developed for further analysis of the 19 recombinants, and showed an approximate distance of 0.57 cM from Rcr1, which was closer to the CR gene than sR6340I.
One of these polymorphisms resulted in loss of a HincII restriction site in the Marquis sequence and was used to develop a CAPS marker (GLP-1/2 CAPs).
Don't adopt a caps bay bee if you are a non-caps, or a non-caps bay bee if you are a caps.
In fact, there's not even a Caps Lock key.
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