Literature DB >> 1916735

Polymorphisms at VNTR loci suggest homogeneity of the white population of Utah.

R Chakraborty1, S P Daiger.   

Abstract

Apparent departure from equilibrium of genetic parameters measured for multiallelic single-locus markers such as VNTR (variable number of tandem repeat) loci has been suggested as evidence of underlying heterogeneity of the tested population. Using allele frequency distributions at eight VNTR loci from the white population of Utah, we show that the observed number of alleles and the gene diversity at each locus are congruent according to expectations of the neutral mutation model. This demonstrates the genetic homogeneity of the white population of Utah with reference to the allele (total and rare) frequency distribution at eight VNTR loci. The importance of such procedures is discussed in the context of using VNTR polymorphism data for forensic and medicolegal applications. Recommendations for reporting population data for hypervariable loci are also made to aid potential users in conducting similar analyses.

Mesh:

Year:  1991        PMID: 1916735

Source DB:  PubMed          Journal:  Hum Biol        ISSN: 0018-7143            Impact factor:   0.553


  13 in total

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Authors:  D E Krane; R W Allen; S A Sawyer; D A Petrov; D L Hartl
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4.  Short alleles revealed by PCR demonstrate no heterozygote deficiency at minisatellite loci D1S7, D7S21, and D12S11.

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Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

5.  Population study of 3 STR loci in the Basque Country (northern Spain).

Authors:  S Alonso; A Castro; I Fernandez; M Gómez de Cedrón; A Garcia-Orad; E Meyer; M Martínez de Pancorbo
Journal:  Int J Legal Med       Date:  1995       Impact factor: 2.686

6.  Evaluation of standard error and confidence interval of estimated multilocus genotype probabilities, and their implications in DNA forensics.

Authors:  R Chakraborty; M R Srinivasan; S P Daiger
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

7.  A computer simulation study of VNTR population genetics: constrained recombination rules out the infinite alleles model.

Authors:  R M Harding; A J Boyce; J J Martinson; J Flint; J B Clegg
Journal:  Genetics       Date:  1993-11       Impact factor: 4.562

8.  Demographic reductions and genetic bottlenecks in humans: minisatellite allele distributions in Oceania.

Authors:  J J Martinson; R M Harding; G Philippon; F F Sainte-Marie; J Roux; A J Boyce; J B Clegg
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

9.  VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach.

Authors:  M D Shriver; L Jin; R Chakraborty; E Boerwinkle
Journal:  Genetics       Date:  1993-07       Impact factor: 4.562

10.  Genetic variation at the ApoB 3'HVR, D2S44, and D7S21 loci in the Ewondo Ethnic Group of Cameroon.

Authors:  G Destro-Bisol; S Presciuttini; E d'Aloja; M Dobosz; G Spedini; V L Pascali
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

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