Literature DB >> 17645485

Combining autosomal and Y-chromosomal short tandem repeat data in paternity testing with male child: methods and application.

Imen Ayadi1, Nadia Mahfoudh-Lahiani, Hafedh Makni, Leila Ammar-Keskes, Ahmed Rebaï.   

Abstract

Paternity testing is being increasingly requested with the aim of challenging presumptive fatherhood. The ability to establish the biological father is usually based on the genotyping of autosomal short tandem repeat (STR) in alleged father, mother and child, but the use of Y-chromosomal STR has gained interest in the last few years. In this work, we propose a new probabilistic approach that combines autosomal and Y-chromosomal STR data in paternity testing with father/son pairs taking into account mutation events. We also suggest a new two-stage approach where we first type Y-STRs and possibly autosomal STR for the putative father and son, conditional on Y-STR results. We applied this approach to 22 cases. Our results show that Y-STRs can identify nonpaternity cases with high accuracy but need to be validated with autosomal STR to establish paternity. Moreover, the two-stage approach is less costly than the standard approach and is very useful in motherless cases.

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Year:  2007        PMID: 17645485     DOI: 10.1111/j.1556-4029.2007.00513.x

Source DB:  PubMed          Journal:  J Forensic Sci        ISSN: 0022-1198            Impact factor:   1.832


  3 in total

1.  Usefulness of SNPs as Supplementary Markers in a Paternity Case with 3 Genetic Incompatibilities at Autosomal and Y Chromosomal Loci.

Authors:  Iris Lindner; Nicole von Wurmb-Schwark; Patrick Meier; Rolf Fimmers; Andreas Büttner
Journal:  Transfus Med Hemother       Date:  2014-02-13       Impact factor: 3.747

2.  Multiplex assay development and mutation rate analysis for 13 RM Y-STRs in Chinese Han population.

Authors:  Wenqiong Zhang; Chao Xiao; Jin Yu; Tian Wei; Fei Liao; Wei Wei; Daixin Huang
Journal:  Int J Legal Med       Date:  2016-11-09       Impact factor: 2.686

3.  Confirmation of Paternity despite Three Genetic Incompatibilities at Chromosome 2.

Authors:  Andrzej Doniec; Wojciech Łuczak; Maria Wróbel; Miłosz Januła; Andrzej Ossowski; Paweł Grzmil; Tomasz Kupiec
Journal:  Genes (Basel)       Date:  2021-01-04       Impact factor: 4.096

  3 in total

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