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Erschienen in: International Journal of Legal Medicine 4/2012

01.07.2012 | Case Report

Maternity exclusion with a very high autosomal STRs kinship index

verfasst von: Li Li, Jianye Ge, Suhua Zhang, Jianzhang Guo, Shumin Zhao, Chengtao Li, Hui Tang, Carey Davis, Bruce Budowle, Yiping Hou, Yacheng Liu

Erschienen in: International Journal of Legal Medicine | Ausgabe 4/2012

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Abstract

This paper reports a maternity testing case to assess the biological relationship between a woman and the boy she was adopting. For all 46 tested autosomal STR loci, the adopting woman and the boy shared at least one allele at each locus, which supported that the woman could be the biological mother of the boy. The pairwise kinship indices (KIs) were calculated for various identity-by-descent distributions. Motherson was the most likely relationship with a very high KI (i.e., 6.91E+08) based on 35 independent autosomal STR loci, but KIs of other pairwise relationships (e.g., aunt–nephew, full sib, etc.) were also high. Further testing of X-STRs and mtDNA excluded the maternity relationship between woman and boy, in which 13 out of 20 X-STR loci were inconsistent and 18 nucleotide mismatches were observed at hypervariable regions I and II of the mtDNA. However, a more distant relationship (e.g., aunt–nephew) cannot be excluded. This case reinforces that possible false identifications can occur in kinship analysis cases yielding very high KIs.
Literatur
1.
Zurück zum Zitat Butler JM (2007) Short tandem repeat typing technologies used in human identity testing. Biotechniques 43(4):ii–vPubMedCrossRef Butler JM (2007) Short tandem repeat typing technologies used in human identity testing. Biotechniques 43(4):ii–vPubMedCrossRef
2.
Zurück zum Zitat Butler JM (2006) Genetics and genomics of core short tandem repeat loci used in human identity testing. J Forensic Sci 51(2):253–265PubMedCrossRef Butler JM (2006) Genetics and genomics of core short tandem repeat loci used in human identity testing. J Forensic Sci 51(2):253–265PubMedCrossRef
3.
Zurück zum Zitat Gjertson DW, Brenner CH, Baur MP, Carracedo A, Guidet F, Luque JA, Lessig R, Mayr WR, Pascali VL, Prinz M, Schneider PM, Morling N (2007) SFG: recommendations on biostatistics in paternity testing. Forensic Sci Int Genet 1(3–4):223–231, Epub 2007 Aug 6PubMedCrossRef Gjertson DW, Brenner CH, Baur MP, Carracedo A, Guidet F, Luque JA, Lessig R, Mayr WR, Pascali VL, Prinz M, Schneider PM, Morling N (2007) SFG: recommendations on biostatistics in paternity testing. Forensic Sci Int Genet 1(3–4):223–231, Epub 2007 Aug 6PubMedCrossRef
4.
Zurück zum Zitat Zhang SH, Li CT, Zhao SM, Li L (2011) Genetic polymorphism of eight X-linked STRs of Mentype® Argus X-8 Kit in Chinese population from Shanghai. Forensic Sci Int Genet 5(1):e21–e24, Epub 2009 Nov 20PubMedCrossRef Zhang SH, Li CT, Zhao SM, Li L (2011) Genetic polymorphism of eight X-linked STRs of Mentype® Argus X-8 Kit in Chinese population from Shanghai. Forensic Sci Int Genet 5(1):e21–e24, Epub 2009 Nov 20PubMedCrossRef
5.
Zurück zum Zitat Walsh PS, Metzger DA, Higuchi R (1991) Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. Biotechniques 10(4):506–513PubMed Walsh PS, Metzger DA, Higuchi R (1991) Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. Biotechniques 10(4):506–513PubMed
6.
Zurück zum Zitat Mentype® Argus X-8 PCR Amplification Kit manual, Biotype® AG, 2007 Mentype® Argus X-8 PCR Amplification Kit manual, Biotype® AG, 2007
7.
Zurück zum Zitat Ge J, Budowle B, Chakraborty R (2010) DNA identification by pedigree likelihood ratio accommodating population substructure and mutations. Investig Genet 1(1):8PubMedCrossRef Ge J, Budowle B, Chakraborty R (2010) DNA identification by pedigree likelihood ratio accommodating population substructure and mutations. Investig Genet 1(1):8PubMedCrossRef
8.
Zurück zum Zitat BØrsting C, Morling N (2011) Mutations and/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers. Forensic Sci Int Genet 5(3):236–241PubMedCrossRef BØrsting C, Morling N (2011) Mutations and/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers. Forensic Sci Int Genet 5(3):236–241PubMedCrossRef
9.
Zurück zum Zitat Phillips C, Fondevila M, Garcĺa-Magarinos M, Rodriguez A, Salas A, Carrecedo A, Lareu MV (2008) Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers. Forensic Sci Int Genet 2(3):198–204PubMedCrossRef Phillips C, Fondevila M, Garcĺa-Magarinos M, Rodriguez A, Salas A, Carrecedo A, Lareu MV (2008) Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers. Forensic Sci Int Genet 2(3):198–204PubMedCrossRef
Metadaten
Titel
Maternity exclusion with a very high autosomal STRs kinship index
verfasst von
Li Li
Jianye Ge
Suhua Zhang
Jianzhang Guo
Shumin Zhao
Chengtao Li
Hui Tang
Carey Davis
Bruce Budowle
Yiping Hou
Yacheng Liu
Publikationsdatum
01.07.2012
Verlag
Springer-Verlag
Erschienen in
International Journal of Legal Medicine / Ausgabe 4/2012
Print ISSN: 0937-9827
Elektronische ISSN: 1437-1596
DOI
https://doi.org/10.1007/s00414-012-0668-8

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