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Marker verification A group of markers are verified together for a control transfer instruction.
The highest number of alleles were detected for the loci RM316 (7) and the lowest was detected for a group of markers viz., RM171, RM284, RM455, RM514, RM277, RM 5795, HvSSR0247, RM 559, RM416 and RM1227.
Furthermore, a group of markers were selected as they were quite stably and highly expressed in all 49 blastomeres, namely DPPA5, FOXD3, HDAC2, RPL19, RPL4, TERT, THY1 and UTF (Table S2).
The LD relationship of haplotypes 4, 5 and 6 10 with markers in the extended PTPN22 haplotype block was examined; all these haplotypes coalesce with the major allele of a group of markers exhibiting very strong inter-marker LD (Figure 1; rs7529353rs11102691, rs11102691 rs11102691).
A prototype represents a group of markers (cluster) assigned to the corresponding array position.
A large inversion of a group of markers was detected in LG7 of Pic.
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In addition, we identified a group of marker genes individuating the japonica and indica subspecies.
This model emphasizes that a group of marker genes is specific to one class.
Each prototype represents a group of marker candidates and corresponds to an average intensity profile of that group.
Based on equations (1), (2), and (3), the first gene in a group of marker genes (the gene associated with g = 1) has the strongest relevance among the members of that group of marker genes.
Accordingly, the gene with the weakest relevance is the last gene in a group of marker genes (the gene associated with g = G).
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