Marker is the band we cloned with the marker named glu-A3a from CS.
For HWA1 mapping, a total of 83 DNA markers distributed on the whole rice genome were used: 24 polymorphic indel markers in Fig. 2, an indel marker named S21074 designed by RGP, another indel marker named Knindel1 (Matsubara et al. 2007), a sequence characterized amplified region (SCAR) marker named d (Ueda et al. 2005), and 56 published SSR markers.
Based on the sequence variations, a CAPS (cleaved amplified polymorphic sequence) marker (named Pi2-LRR) was designed for Pi2.
Therefore, the InDel marker (named Pi9-Pro) can differentiate three different genotypes corresponding to the Pi2/Piz-t, Pi9 and non-Pi2/Piz-t/Pi9 alleles.
To select for gs3 allele from donor GKBR accurately, we developed a SNP marker, named SNP3 (Fig. 2), located within GS3 gene.
In the case of "Paliotto", 8 markers was attached to the canvas vertical edges, and one marker (named F in Fig. 6a, b) was placed on the fixed frame, close to the canvas.
Twenty-seven AFLP markers associated with CM were found and the most promising marker named CGIL4 was then further characterized and mapped to BTA22 q24.
To address this issue, we developed a molecular marker, named DIP STR that relies on pairing deletion insertion polymorphisms (DIP) with STR.
More recently another tumor marker, named CA 72-4 has been identified and characterized using two different monoclonal antibodies B72.3 and CC49.
Our initial mapping using the glossy leaf phenotype as a morphological marker (named Y) mapped the genetic lesion to linkage group A9 from an F2 population derived from a cross between WT and the glossy mutant.
