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94 mutant individuals from F2 were used for primary mapping.
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One set of the RIL population consisting of 252 lines was used for primary QTL mapping.
The homogenate was used for primary screening.
Simple sequence repeat (SSR) markers located at the start of Chr. 5 were used for the primary mapping of NUDA.
The genetic linkage map is derived from 94 F2 mutant individuals for primary mapping and 882 F2 mutant individuals for fine mapping.
Haldane mapping function was used for all mapping calculations.
Sex-averaged linkage map distances were used for QTL mapping.
The previously described genetic map was used for QTL mapping.
Parameters used for the mapping module of the individual maps were same as the consensus map.
These data were used for QTL mapping.
Single-nucleotide polymorphisms (SNPs) are the primary molecular markers used for genetic map construction.
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