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By resequencing a pooled sample of four individuals, we reliably identified loci with a MAF of at least 12.5%.
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By resequencing a 15-kb segment in a human population sample, we were able to narrow the recombinational hotspot to a segment <2 kb in length that coincides with the β-globin replication origin.
The mean expected heterozygosity or genetic diversity within population, Hs (Nei 1987), was estimated for the field Mopti population from Burkina Faso from which field individuals were collected, the Mopti 2003 and the KIL laboratory colonies using single nucleotide polymorphisms (SNP) identified by resequencing of DNA pools.
The first sets of SNP markers were developed by resequencing the European barley gene pool in elite barley genotypes and exploring EST sequences.
For 1416 SNPs and the 30 indels, the polymorphisms were discovered by resequencing the 822 genes from a DNA pool of 24 trees to identify common SNPs (ƒ > 5%; Pelgas et al. 2004).
A single S. pneumoniae resequencing chip with a standard array format of 12.8 mm and feature size of 20×25 micron design capable of resequencing a maximum of 29,375 bases was fabricated by Affymetrix, Inc. (Santa Clara, CA).
In this case, the SNP markers were developed by resequencing the other parent of a mapping population.
Such a possibility would be addressed by resequencing the entire TLR7 region.
Such a possibility would be addressed by resequencing the entire TNIP1 gene.
ACCW verified spot identity by resequencing.
ZFP36*10 was identified by resequencing the EGP subject DNA.
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