Literature DB >> 30278386

Two loci concurrent mutations in non-exclusion parentage cases using 19 STR profiles.

Qiu-Ling Liu1, Ye-Fei Chen2, Yu Zang3, Kai-Yan Liu4, Hu Zhao5, De-Jian Lu6.   

Abstract

Two loci concurrent mutations in non-exclusion paternity case were reported based on 19 STR loci available from Goldeneye™ DNA ID System 20A (Peoplespot, Beijing, China). When 9508 family trios with Paternity index (PI) threshold of >10,000 was analyzed, 14 families show mutations at two loci. The paternity was confirmed by using an additional 19 STR markers. When the probability of occurrence of two mutations was compared with the expected probability deduced from binomial model, the observed mutational probability was significantly larger than the expectation. However, the characteristics of mutations agree with those reported previously. Our result indicates that larger samples is still need to estimate mutation rates accurately and reveal the relationship between mutations with multiple loci and the characterization of human mutations based on microsatellites.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Mutations; Paternity testing; STR

Mesh:

Year:  2018        PMID: 30278386     DOI: 10.1016/j.legalmed.2018.09.012

Source DB:  PubMed          Journal:  Leg Med (Tokyo)        ISSN: 1344-6223            Impact factor:   1.376


  1 in total

1.  Application of CPI cutoff value based on parentage testing of duos and trios typed by four autosomal kits.

Authors:  Hongmei Gao; Chang Wang; Ruxia Zhang; Hanyang Wu; Shanhui Sun; Dongjie Xiao; Yunshan Wang; Maoxiu Zhang
Journal:  PLoS One       Date:  2019-11-13       Impact factor: 3.240

  1 in total

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