A method and system for rapid y-str typing of male individuals
A Y-STR and individual technology, applied in the field of paternity testing, can solve problems such as the increase of time shadow bands, the difficulty of interpreting DNA typing results, and the loss of alleles
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Embodiment 1
[0051] Embodiment 1, verification of the accuracy of the method and system for rapidly obtaining male individual Y chromosome STR typing of the present invention
[0052] In this embodiment, 100 male individual blood samples are used. These samples are samples collected by the applicant from the Physical Evidence Identification Center of the Ministry of Public Security. The source of the individual is unknown, and the method and system of this application are used to type the Y chromosome STR, including:
[0053] 1) Utilize the DNA extraction system in the system of the present invention to extract the DNA of male individuals, 2) Utilize the composite detection system in the system of the present invention to obtain the typing results of the 16 Y chromosome STR loci of the DNA, the STR gene The loci are DYS458, DYS390, DYS438, DYS392, DYS393, DYS437, DYS385a / b, GATA_H4, DYS391, DYS447, DYS19, DYS448, DYS456, DYS635 and DYS439. 3) According to the genotypes of the 16 STR loci, ...
Embodiment 2
[0075] Embodiment 2 The present invention compares the system of male individual Y chromosome STR typing with the existing Y chromosome STR typing kit
[0076] 100 parts of DNA samples of Example 1 are carried out typing of 16 loci with the system of the present application, adopt existing Y chromosome STR typing kit DNATyper Y21 (being conventional detection system) to carry out the typing of above-mentioned sample Y chromosome locus simultaneously Typing, such as Figure 6 (the typing map of 16 loci obtained by the method and system of the present invention) and Figure 7 (The typing map of 16 loci obtained by using the DNATyperY21 kit) is shown.
[0077] With the system of the present invention, compared with the existing Y chromosome STR typing kit (compared, the DNA detection results obtained on the same locus are consistent, and the detection rate all reaches 100%. The results are shown in Table 3, and each group of experiments repeats the results Comprehensive analysi...
Embodiment 3
[0080] Embodiment 3 The sensitivity of the method and system result of the present invention
[0081] Get DNA standard product 9948 10ng, 5ng, 2.5ng, 1.25ng, 625pg, 313pg, 157pg, 78.5pg, 39.3pg and 19.7pg respectively, amplify and detect according to the method provided by the present invention, repeat 3 times in parallel, the result is as follows Figure 3-Figure 4 shown, where image 3 Shows the typing pattern of 16 loci of the standard DNA 9948 (10ng) obtained by the method and system of the present invention, Figure 4 The statistical results of the sensitivity test of the system of the present invention are shown.
[0082] Depend on Figure 4 It can be seen that the optimum DNA template amount of the inventive method is between 157pg~1.25ng, and when the template amount is 78.5pg or below, although complete STR typing can still be obtained, some allele peak heights are lower than 50RFU; When the amount of DNA template is 39.3pg or lower, alleles may be lost, and comple...
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