A general method to assess the utility of the X-chromosomal markers in kinship testing

被引:20
|
作者
Pinto, Nadia [1 ,2 ,3 ]
Silva, Pedro V. [2 ,3 ]
Amorim, Antonio [1 ,2 ]
机构
[1] Univ Porto, Inst Patol & Imunol Mol, P-4200465 Oporto, Portugal
[2] Univ Porto, Fac Ciencias, P-4200465 Oporto, Portugal
[3] Univ Porto, Ctr Matemat, P-4200465 Oporto, Portugal
关键词
Genetic evidence; Kinship testing; Identity-by-descent; X-chromosome; Genotypic probabilities; Distinguishing pedigrees; IDENTIFICATION;
D O I
10.1016/j.fsigen.2011.04.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In studies involving pedigree reconstruction and kinship estimation, it is acknowledged that some pedigrees have the same algebraic expressions for the joint genotypic probabilities and are, therefore, indistinguishable when considering only genetic information, no matter what the mode of transmission considered. Indeed, although standard forensic practice considers solely unlinked autosomal markers, the existence of pedigrees with the referred theoretical property (that are then said to belong to the same kinship class) is possible when considering any kind of genetic transmission. The research on genetic relatedness has always been linked to the root concept of identity-by-descent (IBD). However, although the basic theoretical core for autosomal transmission has been long formalised, a general method allowing the decision if two pedigrees linking two non-inbred individuals are distinguishable using unlinked autosomal markers along with the respective IBD partitions (and consequently the algebraic expressions for the joint genotypic probabilities) was only recently published. In this work X-chromosomal transmission will be at stake, considering that the analytical framework for X-chromosomal markers has been recently established and the importance of X-chromosome markers for these questions has been steadily growing, particularly in forensics, as a tool both to complement the information given by autosomes in complex kinship testing cases and to differentiate pedigrees belonging to the same autosomal kinship class. Therefore, here it will be presented a formal and mathematically well supported framework where a general counting rule is given, allowing a secure and expeditious decision on the usefulness of typing (unlinked) X-chromosomal markers on pairwise kinship testing involving two non-inbred individuals. Moreover the counting rule now presented allows the derivation of algebraic expressions for the joint genotypic probabilities associated with any pedigree. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:198 / 207
页数:10
相关论文
共 42 条
  • [21] ANONYMOUS X-CHROMOSOMAL PROBES REVEALING DNA POLYMORPHISMS USEFUL AS GENETIC-MARKERS FOR X-LINKED DISEASES
    ALBERTSEN, HM
    AHRENS, P
    VESTERGAARD, SR
    JORGENSEN, B
    KRUSE, TA
    BOLUND, L
    SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1986, 46 : 136 - 136
  • [22] Genetic structure and polymorphisms of Gelao ethnicity residing in southwest china revealed by X-chromosomal genetic markers
    Chen, Pengyu
    He, Guanglin
    Zou, Xing
    Wang, Mengge
    Luo, Haibo
    Yu, Limei
    Hu, Xijie
    Xia, Mijia
    Gao, Hongyan
    Yu, Jian
    Hou, Yiping
    Han, Yanyan
    SCIENTIFIC REPORTS, 2018, 8
  • [23] Paternity exclusion power: Comparative behaviour of autosomal and X-chromosomal markers in standard and deficient cases with inbreeding
    Pinto, Nadia
    Gusmao, Leonor
    Egeland, Thore
    Amorim, Antonio
    FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2013, 7 (02) : 290 - 295
  • [24] The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers
    Vania Pereira
    Carmen Tomas
    Juan J Sanchez
    Denise Syndercombe-Court
    António Amorim
    Leonor Gusmão
    Maria João Prata
    Niels Morling
    European Journal of Human Genetics, 2015, 23 : 245 - 251
  • [25] Genetic structure and polymorphisms of Gelao ethnicity residing in southwest china revealed by X-chromosomal genetic markers
    Pengyu Chen
    Guanglin He
    Xing Zou
    Mengge Wang
    Haibo Luo
    Limei Yu
    Xijie Hu
    Mijia Xia
    Hongyan Gao
    Jian Yu
    Yiping Hou
    Yanyan Han
    Scientific Reports, 8
  • [26] The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers
    Pereira, Vania
    Tomas, Carmen
    Sanchez, Juan J.
    Syndercombe-Court, Denise
    Amorim, Antonio
    Gusmao, Leonor
    Prata, Maria Joao
    Morling, Niels
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (02) : 245 - 251
  • [27] What is the Clinical Utility of Chromosomal Microarray Testing in General Child Neurology Practice?
    Le Pichon, J. B.
    Luniova, A.
    Yuen, J.
    Abdelmoity, A.
    Allaboun, K.
    Sherman, A.
    Haney, C.
    Yu, S.
    Graf, W. D.
    ANNALS OF NEUROLOGY, 2012, 72 : S198 - S198
  • [28] Testing for goodness rather than lack of fit of an X-chromosomal SNP to the Hardy-Weinberg model
    Wellek, Stefan
    Ziegler, Andreas
    PLOS ONE, 2019, 14 (02):
  • [29] Genetic portrait of North-West Indian population based on Autosomal and X-chromosomal Alu insertion markers
    Singh, Gagandeep
    Sandhu, Harkirat Singh.
    Talwar, Indu
    Bhanwer, A. J. S.
    AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, 2020, 171 : 263 - 263
  • [30] Testing Sex-Biased Admixture Origin of Macaque Species Using Autosomal and X-Chromosomal Genomic Sequences
    Osada, Naoki
    Matsudaira, Kazunari
    Hamada, Yuzuru
    Malaivijitnond, Suchinda
    GENOME BIOLOGY AND EVOLUTION, 2021, 13 (01):