Sentence examples for peak markers from inspiring English sources

Sequences corresponding to the peak markers for qBK1_628091 and qBK4_31750955 are here provided (Additional file 6: Figure S5).

Based on this initial genotyping, plants possessing the peak markers were selected and all the remaining foreground SSR markers were ran on selected plants.

The selection process started with foreground genotyping where the qDTY loci were monitored by three peak markers, with one peak marker for each qDTY locus.

During the 2011 WS, 734 F1(3) plants from seeds of the three plants (IR 97978, IR 97982, and IR 97989) were genotyped using three peak markers.

This interval was also located between the two peak markers identified in a previously reported anaerobic germination-associated QTL (qAG1-2, 26.04–32.03 Mb) (Angaji et al. 2010).

The peak markers linked to the three qDTY regions on chromosome 2, 3, and 12 were RM12460, RM520, and RM511, respectively (Table 4).

Peak marker Flanking markers IM LOD IM R2 Add.

The peak marker was at 31.0 Mb (Fig. 3a and Table 1).

We determined mean residence time (MRT) and peak marker concentration using the original profile observations and regressions.

Mean residence and peak marker concentration times, which reflect marker profile shape, did not strongly differ by diet (P=0.434, 0.0824) or site (P=0.113, 0.0824), though they did by cow (P=0.036, 0.004).

However, the reported peak marker RM236 for qDTY 2.2 (Swamy et al. 2013) was replaced with RM12460 (the closest polymorphic marker in the qDTY 2.2 region) as RM236 was monomorphic among MRQ74 and the qDTY 2.2 donor.