New short nucleotide tandem repeat site and application thereof
A short tandem repeat and nucleotide sequence technology, applied in the field of short nucleotide tandem repeat sequence sites, can solve the problems of poor compatibility and achieve high compatibility, high heterozygosity, and high resolution
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Embodiment 1
[0154] Combine the new STR locus G7S0005 of the present invention with 10 commonly used gene loci (VWA, D16S539, D5S818, D7S820, D13S317, D8S1179, D18S51, TH01, D2S1338, AMELO), and use multiple fluorescent PCR technology to check the samples, 4 used The samples were a sample of a family of three with a relationship, and a control sample with no relationship. The primer sequences of G7S0005 and 10 commonly used loci are shown in Table 2.
[0155] Table 2 Primer sequence
[0156]
[0157] Note: Four fluorescent dyes: PET, VIC, NED, and FAM (Applied Biosystems, USA).
[0158]
[0159] The specific experimental operation steps are as follows:
[0160] 1) DNA sample preparation
[0161] Collect blood from 4 selected individual samples; extract DNA samples with DNA extraction kit and take 1μl each, perform quality inspection and concentration estimation of the samples with 1% agarose electrophoresis, and then dilute the samples to working concentration according to the estimated concentrati...
Embodiment 2
[0175] Twenty groups of samples with and without genetic relationship were randomly selected, and the method of Example 1 was used for detection, except that only the new STR locus G7S0005 of the present invention was used.
[0176] After testing, after determining the paternal samples, determine the offspring samples of the remaining 19 groups of samples that are related to the paternal parent. The new STR locus G7S0005 of the present invention can accurately exclude the 6 groups of unrelated samples. A high degree of discrimination.
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