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Impact of a chromosome X STR Decaplex in deficiency paternity cases

Deficiency paternity cases, characterized by the absence of the alleged father, are a challenge for forensic genetics. Here we present four cases with a female child and a deceased alleged father in which the analysis of a set of 21 or 22 autosomal STRs (AS STRs) produced results within a range of d...

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Autores principales: Trindade-Filho, Aluisio, Ferreira, Samuel, Oliveira, Silviene F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873181/
https://www.ncbi.nlm.nih.gov/pubmed/24385853
http://dx.doi.org/10.1590/S1415-47572013000400008
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author Trindade-Filho, Aluisio
Ferreira, Samuel
Oliveira, Silviene F.
author_facet Trindade-Filho, Aluisio
Ferreira, Samuel
Oliveira, Silviene F.
author_sort Trindade-Filho, Aluisio
collection PubMed
description Deficiency paternity cases, characterized by the absence of the alleged father, are a challenge for forensic genetics. Here we present four cases with a female child and a deceased alleged father in which the analysis of a set of 21 or 22 autosomal STRs (AS STRs) produced results within a range of doubt when genotyping relatives of the alleged father. Aiming to increase the Paternity Index (PI) and obtain more reliable results, a set of 10 X-linked STR markers, developed by the Spanish and Portuguese Group of the International Society for Forensic Genetics (ISFG), was then added. Statistical analysis substantially shifted the results towards the alleged fatherhood in all four cases, with more dramatic changes when the supposed half-sister and respective mother were the relatives tested.
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spelling pubmed-38731812014-01-02 Impact of a chromosome X STR Decaplex in deficiency paternity cases Trindade-Filho, Aluisio Ferreira, Samuel Oliveira, Silviene F. Genet Mol Biol Human and Medical Genetics Deficiency paternity cases, characterized by the absence of the alleged father, are a challenge for forensic genetics. Here we present four cases with a female child and a deceased alleged father in which the analysis of a set of 21 or 22 autosomal STRs (AS STRs) produced results within a range of doubt when genotyping relatives of the alleged father. Aiming to increase the Paternity Index (PI) and obtain more reliable results, a set of 10 X-linked STR markers, developed by the Spanish and Portuguese Group of the International Society for Forensic Genetics (ISFG), was then added. Statistical analysis substantially shifted the results towards the alleged fatherhood in all four cases, with more dramatic changes when the supposed half-sister and respective mother were the relatives tested. Sociedade Brasileira de Genética 2013-12 2013-11-08 /pmc/articles/PMC3873181/ /pubmed/24385853 http://dx.doi.org/10.1590/S1415-47572013000400008 Text en Copyright © 2013, Sociedade Brasileira de Genética. License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Human and Medical Genetics
Trindade-Filho, Aluisio
Ferreira, Samuel
Oliveira, Silviene F.
Impact of a chromosome X STR Decaplex in deficiency paternity cases
title Impact of a chromosome X STR Decaplex in deficiency paternity cases
title_full Impact of a chromosome X STR Decaplex in deficiency paternity cases
title_fullStr Impact of a chromosome X STR Decaplex in deficiency paternity cases
title_full_unstemmed Impact of a chromosome X STR Decaplex in deficiency paternity cases
title_short Impact of a chromosome X STR Decaplex in deficiency paternity cases
title_sort impact of a chromosome x str decaplex in deficiency paternity cases
topic Human and Medical Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873181/
https://www.ncbi.nlm.nih.gov/pubmed/24385853
http://dx.doi.org/10.1590/S1415-47572013000400008
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