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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2013
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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. |
format | Online Article Text |
id | pubmed-3873181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Sociedade Brasileira de Genética |
record_format | MEDLINE/PubMed |
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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