SNP-STR analysis for non-invasive paternity test for fetus
SNP-STR analysis for non-invasive paternity test for fetus
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SNP-STR分析用于胎儿无创亲子鉴定
DOI:
10.1016/j.fsigss.2017.09.157
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发表时间:
2017-12-01
期刊:
影响因子:
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通讯作者:
Liang, W. B.
中科院分区:
文献类型:
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作者:
Wang, L.;Li, Y.;Liang, W. B.
The existence of cell-free fetal (cff) DNA in maternal plasma through the process of pregnancy, makes it possible to do noninvasive paternity test for a woman who got pregnant as a result of a sexual assault. However, the cff DNA in a high background of maternal DNA could not be easily detected. The SNP-STR markers, developed for analyzing the minor component in a two-man unbalanced mixture, were used for noninvasive paternity identification during pregnancy. Six SNP-STR loci, rs4847015-D1S1656, rs6736691-D2S1338, rs25768-D5S818, rs7786079-D7S820, rs2246512-D10S1248, rs11642858-D16S539, were screened based on autosomal STRs of Expanded U.S. Core Loci, and the corresponding primers were designed by amplification refractory mutation system (ARMS) method. The primers for every loci consisted of two forward primers targeting the genotype of SNP and one reverse primer, and each forward primer was amplified with the reverse one respectively. The amplicons of the six loci were all less than 210 bp. The cff DNA of plasma samples from ten pregnant women at 16 to 22-week was detected using the informative makers selected from the analysis of maternal and biological paternal DNA by SNP-STR PCR. The results demonstrate the availability of SNP-STR in the noninvasive paternity test.