Figure 2From: A high-throughput method for the detection of homoeologous gene deletions in hexaploid wheatAlignment of TaPFT1 homoeologues. 'A', 'B' and 'D' TaPFT1 homoeologue sequences in regions used for design of the probe assay (A) and the CAPS assay (B), respectively (see Figure 1) were aligned. Forward and reverse primers used in the probe assay are highlighted in blue. Polymorphisms are highlighted in red. In (A), homoeologue specific probe sequences and in (B), restriction enzyme (Hpy166II) cleavage sites are highlighted in yellow.Back to article page