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In conclusion, the SynOpDH high-density map provides a large number of markers for wheat genome analysis and gene mapping.
It was expected that the study would identify important genes and functional markers for wheat yield improvement.
In this review, three markers for wheat grain weight genes were also mentioned; they were TaSus2-2B, Tand2-6A and TaCwi-A1[ 19, 41, 42], respectively.
We have shown that ESTs are a good source of SSRs that can be exploited to develop microsatellite markers for wheat, barley and rice.
Consequently, when developing EST-PCR markers for wheat, it is essential to eliminate EST sequences derived from paralogous genes and to establish a method to efficiently sort products derived from homoeologous genes.
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Glucose can be considered as a marker for wheat adulteration and fructose for soybean, respectively.
Data are used to assess the distribution of diversity among and within wheat genomes and to develop a panel of SNP markers for polyploid wheat.
Identification of unique SNP markers and knowledge of the locations of unique clusters can be used as a first step in the preparation of cultivar-specific markers for bread wheat.
The results indicated that there is strong agreement between the independent de novo linkage map and the POPSEQ mapping approach in mapping and ordering GBS markers for hexaploid wheat.
With this system, it is now possible to sort homoeologous genes using a low-cost and convenient separation method, thus allowing large-scale PCR-based marker development for wheat.
The main purpose of this study was to investigate the distribution of Puroindoline-D1 alleles in landraces and introduced cultivars of the Yellow and Huai Valley of China, in order to further characterize the molecular mechanism of PINA-null alleles, and to develop a robustly PCR-based molecular marker approach for wheat breeding.
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