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The availability of genome scan technology, capable of genotyping individuals at hundreds of thousands of markers has made this observational approach possible.
The use of Y chromosomal genetic markers has made important contributions to studies of evolution, male-specific demography, and sexual selection in humans [1] [4].
The development of large numbers of SNP markers has made population based genome-wide association testing increasingly feasible [25], [26], [27], [28].
The development of more reliable serum markers has made their use easier.
The development of DNA markers has made it possible to study the naturally occurring allelic variation controlling quantitative traits loci (QTL).
Paucity of genetic data such as genome sequences, transcriptome sequences and associated molecular markers has made Primula breeding or evolutionary analysis a challenging task.
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Molecular markers have made it possible to identify and pyramid valuable genes of agronomic importance in resistance rice breeding.
Genetic markers have made it possible to detect QTLs that are significantly associated with traits, making selection more effective [ 21].
8 To date, however, few of these markers have made the transition from research to clinical practice.
Genetic markers have made it possible to detect QTL that are significantly associated with traits [ 2], and made selection more effective.
Genetic markers have made it possible to detect QTLs that are significantly associated with traits, and made selection more effective [ 3].
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