Fetus chromosome aneuploid genome sequencing detection method
A genome sequencing and aneuploidy technology, which is applied in the determination/inspection of microorganisms, biochemical equipment and methods, etc., can solve the problems of lack of detection methods, steps, and uneven levels of detection methods, so as to ensure accuracy, prevent Chromosomal mutation, reducing the effect of disease
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[0027] The embodiment of the present invention provides a method for genome sequencing detection of fetal chromosomal aneuploidy, comprising the following steps:
[0028] s1: Sampling, taking peripheral blood containing fetal DNA from pregnant women;
[0029] s2: DNA extraction, DNA extraction, and concentration;
[0030] s3: Check, use high-throughput sequencing technology to scan the whole genome and conduct bioinformatics analysis;
[0031] S4: output the result.
[0032] By testing the fetus at about 12 to 22 weeks of gestation, if the fetus has chromosome deletion or polychromosomal conditions in the test, we recommend terminating the pregnancy, and the pregnancy work is relatively simple at this time, in order to ensure the safety of pregnant women and their family harmony , the present invention is through multiple rounds simultaneously, and each round carries out multiple (three times) detection, guarantees the accuracy of detection, guarantees no error, prevents tha...
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