Complex casework using single nucleotide polymorphisms

被引:0
|
作者
Dario, Paulo [1 ,2 ,3 ,4 ]
Ribeiro, Teresa [1 ,2 ]
Dias, Deodalia [3 ,4 ]
Corte-Real, Francisco [1 ,2 ,5 ]
Geada, Helena [2 ,6 ]
机构
[1] Natl Inst Legal Med, Coimbra, Portugal
[2] CENCIFOR, Forens Sci Ctr, Coimbra, Portugal
[3] CESAM Ctr Environm & Marine Studies, Lisbon, Portugal
[4] Univ Lisbon, Fac Sci, Lisbon, Portugal
[5] Univ Coimbra, Fac Med, Coimbra, Portugal
[6] Univ Lisbon, Fac Med, Lisbon, Portugal
关键词
Autosomal SNPs; Complex kinship testing; SNaPshot((R));
D O I
10.1016/j.fsigss.2011.09.051
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Complex kinship analyses are normally a challenge for forensic laboratories, especially in cases in which the individuals involved can have criminal responsibilities. This paper presents two complex relationship caseworks studied with routine STRs and autosomal SNPs as supplementary markers. In the first case, to exclude trafficking of children, maternity investigation of a child was requested involving two alleged mothers - 39-year-old woman, the alleged grandmother, and her absent daughter. The second one was a possible incest case with a young girl with Trisomy 21 where her father was also the alleged child's father. The individuals of these cases were typed for 17 autosomal STRs with AmpFlSTR Identifiler or IdentifilerPlus and Powerplex 16. Twenty autosomal SNPs were also typed using SNaPshot((R)) methodology, with two 10-plex previously revealed useful in paternity testing. Both cases gave low likelihood ratio values with STRs and a genetic incompatibility was also detected in the first case. SNP studies strongly indicated that the alleged grandmother was not the child's mother but indeed the grandmother in a real complex immigrant kinship case, while in the second casework reinforced the incest relationship. Therefore, SNPs revealed useful as additional markers in complex kinship testing. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:E379 / E380
页数:2
相关论文
共 50 条
  • [41] Classifying single nucleotide polymorphisms in humans
    Shima Azizzadeh-Roodpish
    Max H Garzon
    Sambriddhi Mainali
    Molecular Genetics and Genomics, 2021, 296 : 1161 - 1173
  • [42] Single nucleotide polymorphisms of the fukutin gene
    Cao, H
    Yuen, J
    Hegele, RA
    JOURNAL OF HUMAN GENETICS, 2001, 46 (08) : 487 - 489
  • [43] Automation in genotyping of single nucleotide polymorphisms
    Gut, IG
    HUMAN MUTATION, 2001, 17 (06) : 475 - 492
  • [44] SINGLE NUCLEOTIDE POLYMORPHISMS AND SUICIDAL BEHAVIOUR
    Pregelj, Peter
    PSYCHIATRIA DANUBINA, 2012, 24 : S61 - S64
  • [45] Population specific single nucleotide polymorphisms
    Phillips, C
    Lareu, M
    Salas, A
    Fondevila, M
    Lee, GB
    Carracedo, A
    Morling, N
    Schneider, P
    Court, DS
    PROGRESS IN FORENSIC GENETICS 10, 2004, 1261 : 233 - 235
  • [46] A tool for mapping Single Nucleotide Polymorphisms using Graphics Processing Units
    Manconi, Andrea
    Orro, Alessandro
    Manca, Emanuele
    Armano, Giuliano
    Milanesi, Luciano
    BMC BIOINFORMATICS, 2014, 15 : 1 - 13
  • [47] Predicting Amino Acid Substitution Probabilities Using Single Nucleotide Polymorphisms
    Rizzato, Francesca
    Rodriguez, Alex
    Biarnes, Xevi
    Laio, Alessandro
    GENETICS, 2017, 207 (02) : 643 - 652
  • [48] Spectrofluorometric genotyping of single nucleotide polymorphisms using carbon dots as fluorophores
    Motaghi, Hasan
    Mehrgardi, Masoud Ayatollahi
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2019, 206 : 154 - 159
  • [49] Eye color prediction using single nucleotide polymorphisms in Saudi population
    Alghamdi, Jahad
    Amoudi, Manal
    Kassab, Ahmad Ch
    Al Mufarrej, Mansour
    Al Ghamdi, Saleh
    SAUDI JOURNAL OF BIOLOGICAL SCIENCES, 2019, 26 (07) : 1607 - 1612
  • [50] A tool for mapping Single Nucleotide Polymorphisms using Graphics Processing Units
    Andrea Manconi
    Alessandro Orro
    Emanuele Manca
    Giuliano Armano
    Luciano Milanesi
    BMC Bioinformatics, 15