1998
DOI: 10.1016/s0379-0738(98)00079-6
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Regional genetic variation in Caucasians

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Cited by 20 publications
(12 citation statements)
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“…For D2 and D3, close agreement is again obtained with separate estimates reported in Watson et al (2000). As observed previously in analyses of SGM data (Foreman et al 1998;Foreman and Lambert 2000), allele distributions exhibited at the new loci are very similar within racial groups (see Figs. 2,3).…”
Section: Allele Distributions and Discriminating Powersupporting
confidence: 88%
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“…For D2 and D3, close agreement is again obtained with separate estimates reported in Watson et al (2000). As observed previously in analyses of SGM data (Foreman et al 1998;Foreman and Lambert 2000), allele distributions exhibited at the new loci are very similar within racial groups (see Figs. 2,3).…”
Section: Allele Distributions and Discriminating Powersupporting
confidence: 88%
“…F ST estimates are small (e.g. Gill and Evett 1995;Foreman et al 1998). Recognition of all these issues culminates in the paradoxical situation where authors describe the results of significance testing on DNA profiling data in order to justify the independence assumptions underlying the forensic calculations to be used in practice, only to ignore or "explain away" any significant results which are obtained as being of no practical consequence (e.g.…”
Section: A Foreman · I W Evettmentioning
confidence: 99%
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“…An LR was used to quantify the strength of a match between a urine sample and the corresponding blood sample. LRs per locus were calculated using the formula of Balding and Nichols [15], using θ=0.01 to represent the level of co-ancestry within the Caucasian population [16]. Individual LRs were multiplied across loci.…”
Section: Discussionmentioning
confidence: 99%
“…The overall F ST estimate for the 10 loci was 0.002 (bootstrap confidence interval upper bound = 0.0034) with F ST values for individual loci ranging up to 0.0052 (D8S1179). This indicates that there is a level of coancestry similar to other European populations in Norway [3,4], and applying a u value of 0.01 would be sufficient to take account of the effect of population substructure when estimating match probabilities. The frequency of the theoretically most common genotype is www.elsevier.com/locate/forsciint Forensic Science International 170 (2007) 59-61 Table 1 Allele frequencies for AmpFlSTR SGM plus loci in a Norwegian population sample of 1000 individuals Allele D3S1358 vWA D16S539 D2S1338 D8S1179 D21S11 D18S51 D19S433 TH01 FGA 5 --------0.005 -6 --------0.209 -7 - 2.65 Â 10 À10 .…”
mentioning
confidence: 99%