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Development of high-density genetic markers in the QTL regions of specific mapping populations is essential for fine-mapping and map-based cloning of economically important genes.
The main limitation with QTL detection in these mapping populations is the large size of the confidence interval.
So, before using these QTLs/genes in MAS further validation on a large panel of high Zn donor lines and Zn specific biparental mapping populations is essential.
The extension to other experimental mapping populations is straightforward.
Linkage disequilibrium (LD) in linkage mapping populations is caused by genetic linkage [ 9].
Segregation distortion in mapping populations is a well-documented phenomenon in different crops [ 41, 42].
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The genotypic data for the two mapping populations were downloaded from http://ricediversity.org/data.org/data
The parental lines of two mapping populations were exposed to a pulse stress of 1,000 mg L−1 Fe2+ in hydroponics.
Two mapping populations were used for linkage mapping in this study.
The commonality is that all the individuals in the mapping populations are inbred lines.
Two mapping populations were used to map the polymorphic markers.
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