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The 37 remaining markers represented a wide variety of repeat motif and length (Table 1) and were located on 37 different contigs.
According to a study using dairy cattle data by Weigel et al. [ 21], moving from a set of 300 markers to a set of 2000 markers represented a gain in accuracy of ~30% or ~113%, depending on how the subsets of markers were selected (with largest effects or equally spaced).
Although, the tetranucleotide repeat markers represented a level of instability five times higher than dinucleotide repeats supporting the functional overlap of MutS β and MutS α in IDL2 repair, low dinucleotide repeat instability was caused by defected MutS β (MSH3) (Haugen et al, 2008).
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These markers represented an amount of money comparable to the average annual expenditure by Medicare enrollees in 2007 as identified in Medicare claims files.
Moreover these markers represent a tool to assess PDAC mutational landscape.
The relative paucity of cell-restricted markers represents a current constraint on physiological and pathophysiological studies of the adult murine epicardium.
These markers represent a valuable resource for future comparative genome analysis.
However, these markers represent a very small proportion of the spruce genome.
These markers represent a significant addition to the limited set of genic-SSR markers available in pigeonpea [ 16- 20].
The recent Ae. tauschii genetic map contained 7,185 SNP markers, representing a great resource for the D genome.
These markers (representing a total of 71 loci) were mapped to the previously reported RG × H genetic linkage map.
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