Literature DB >> 24632058

Genetic polymorphisms of twelve X-STRs of the investigator Argus X-12 kit and additional six X-STR centromere region loci in an Egyptian population sample.

S Elakkary1, S Hoffmeister-Ullerich2, C Schulze2, E Seif3, A Sheta3, S Hering4, J Edelmann5, C Augustin6.   

Abstract

Recently, many researchers have focused on analysis of different X-chromosomal STRs as they bear the potential to efficiently complement the analysis of autosomal and Y-chromosomal STRs in solving special complex kinship deficiency cases. In the current study we examined a sample of 250 unrelated Egyptian males with the Investigator Argus X-12 kit (Qiagen GmbH, Hilden, Germany) which detects 12 X-STR markers distributed over the entire X-chromosome as four closely linked clusters. Microvariant off ladder alleles as well as null alleles have been detected in some loci. Furthermore, discordant results were observed between the Investigator Argus X-12 and the Mentype(®) Argus X-8 kits (Biotype AG, Dresden, Germany). New primers were designed for loci DXS10101, DXS10146 and DXS10148 to correct the allele drop outs observed in these loci with the Investigator Argus X-12 kit. Additionally, DNA sequence analysis revealed the polymorphisms responsible for the allele drop outs. Furthermore, six additional X-STRs (DXS10161, DXS10159, DXS10162, DXS10163, DXS10164 and DXS10165) located in the centromere region at Xp11.21-Xq11.1 were examined in a single multiplex reaction. Allele and haplotype frequencies as well as different forensic statistical parameters of the 18 X-STR loci tested indicated that they are highly informative in different forensic applications in the Egyptian population. However, some modifications still need to be performed on the Investigator Argus X-12 kit before its use in forensic casework is validated.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

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Keywords:  Egypt; Haplotype frequencies; Microvariant alleles; Null alleles; Sequencing

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Year:  2014        PMID: 24632058     DOI: 10.1016/j.fsigen.2014.02.007

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  2 in total

1.  Polymorphism and haplotype analysis of three novel short tandem repeat loci in the p11.4 region of human X chromosome.

Authors:  Takeki Nishi; Kenji Fukui; Sari Matumoto; Shojiro Takasu; Kimiharu Iwadate
Journal:  Int J Legal Med       Date:  2021-11-06       Impact factor: 2.791

2.  Haplotype data and forensic evaluation of 23 Y-STR and 12 X-STR loci in eight ethnic groups from Eritrea.

Authors:  Carla Bini; Stefania Sarno; Elisabetta Tangorra; Alessandra Iuvaro; Sara De Fanti; Yohannes Ghebremedhin Tseghereda; Susi Pelotti; Donata Luiselli
Journal:  Int J Legal Med       Date:  2020-10-22       Impact factor: 2.686

  2 in total

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