2005
DOI: 10.1016/j.forsciint.2004.09.118
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Allelic frequencies of 13 STR loci in autochthonous Basques from the province of Vizcaya (Spain)

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Cited by 11 publications
(10 citation statements)
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“…STRs have become one of the most widely used genomic markers in several fi elds, including genetic mapping, linkage analysis and human identity testing, due to their hypervariable nature. This feature makes STRs valuable markers in molecular taxonomic studies with evolutionary perspective and in the elucidation of human population history [10][11][12][13][14][15][16] .…”
Section: Introductionmentioning
confidence: 99%
“…STRs have become one of the most widely used genomic markers in several fi elds, including genetic mapping, linkage analysis and human identity testing, due to their hypervariable nature. This feature makes STRs valuable markers in molecular taxonomic studies with evolutionary perspective and in the elucidation of human population history [10][11][12][13][14][15][16] .…”
Section: Introductionmentioning
confidence: 99%
“…These STRs constitute the core of PCR-based genetic markers in the US-combined DNA index system (CODIS). In addition, STR allelic frequency data previously reported by our research team from two Basque groups from the provinces of Alava and Vizcaya were included in our analyses to augment the geographical scope of our study (Pe´rez-Miranda et al 2005a, 2005b. Finally, for the purposes of assessing population affinities and phylogenetic relationships with other human groups, European (including Spain), North African, and Middle Eastern populations were jointly analyzed.…”
Section: Introductionmentioning
confidence: 99%
“…(STRs) represents hypervariable regions that can provide the fine resolution needed to determine relationships among closely related populations in recent evolutionary history (Bowcock et al 1994;Jorde et al 1995Jorde et al , 1997Bosch et al 2000;Lum et al 2002;Rowold and Herrera 2003;Pérez-Miranda et al 2005;Shepard and Herrera 2005) and the discrimination power essential for robust individual probabilities of inclusion (Leibelt et al 2003;Collins et al 2004). Also, STRs are used in these studies because of their numerous and relatively even distribution throughout the genome, high levels of polymorphism, a large number of possible alleles per locus, and short amplicon lengths, which facilitate DNA amplification, separation, and detection (Butler 2001;Butler et al 2003).…”
mentioning
confidence: 99%