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A F2 population derived from the RHL was used for fine mapping.
836 individuals with yellow-green leaf phenotype in F2 population were used for fine mapping.
This segregating population was used for fine mapping of the GNS4 locus.
Then a larger F2 population with 4213 mutant individuals was used for fine mapping.
To narrow the candidate region for sor1, 647 F2 plants were used for fine mapping.
Molecular markers used for fine mapping of the sug-h mutant.
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VDR, CYP27B1 and all SNPs used for finer mapping were assayed with the Sequenom MassArray platform [7].
Increasing the number of meioses within a mapping population by generating advanced-generation crosses can be used for finer mapping of QTL, but this approach is impractical with perennial plants because of the length of time required to produce and collect phenotypic data from each generation.
Single nucleotide polymorphisms (SNPs) have emerged as genetic markers of choice because of their high density and relatively even distribution in the human genomes [ 3, 4], and are being using for fine mapping of disease loci and for candidate gene association studies.
The full F2 mapping population of 1599 individuals was used for fine-mapping.
F2 3 families were used for QTL identification, and the other populations were used for fine-mapping of the major QTL qRgls2.
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used for fine image
used for fine control
used for fine ritual
used for further mapping
used for fine adjustment
used for fine needle
used for fine scale
used for fine blasting
used for fine furniture
used for comparative mapping
used for fine dining
used for fine convergence
used for homogeneous mapping
used for fine regulation
used for genetic mapping
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