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A case of false mother included with 46 autosomal STR markers.


ABSTRACT: BACKGROUND:For solving a maternity case, 19 autosomal short tandem repeats (STRs) were amplified using the AmpF?STR(®) Sinofiler(TM) kit and PowerPlex(®) 16 System. Additional 27 autosomal STR loci were analyzed using two domestic kits AGCU 21+1 and STRtyper-10G. The combined maternity index (CMI) was calculated to be 3.3?×?10(13), but the putative mother denied that she had given birth to the child. In order to reach an accurate conclusion, further testing of 20 X-chromosomal short tandem repeats (X-STRs), 40 single nucleotide polymorphism (SNP) loci, and mitochondrial DNA (mtDNA) was carried out. FINDINGS:The putative mother and the boy shared at least one allele at all 46 tested autosomal STR loci. But, according to the profile data of 20 X-STR and 40 SNP markers, different genotypes at 13 X-STR loci and five SNP loci excluded maternity. Mitochondrial profiles also clearly excluded the mother as a parent of the son because they have multiple differences. It was finally found that the putative mother is the sister of the biological father. CONCLUSIONS:Different kinds of genetic markers needfully supplement the use of autosomal STR loci in case where the putative parent is suspected to be related to the true parent.

SUBMITTER: Li L 

PROVIDER: S-EPMC4487102 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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A case of false mother included with 46 autosomal STR markers.

Li Li L   Lin Yuan Y   Liu Yan Y   Zhu Ruxin R   Zhao Zhenmin Z   Que Tingzhi T  

Investigative genetics 20150630


<h4>Background</h4>For solving a maternity case, 19 autosomal short tandem repeats (STRs) were amplified using the AmpFℓSTR(®) Sinofiler(TM) kit and PowerPlex(®) 16 System. Additional 27 autosomal STR loci were analyzed using two domestic kits AGCU 21+1 and STRtyper-10G. The combined maternity index (CMI) was calculated to be 3.3 × 10(13), but the putative mother denied that she had given birth to the child. In order to reach an accurate conclusion, further testing of 20 X-chromosomal short tand  ...[more]

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