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Is there a problem in obtaining the report by non-invasive dna SMS notification?
Non-invasive DNA prenatal testing mainly screens whether the fetus has three common chromosomal diseases: T2 1 (Down syndrome), T 18 (Edward syndrome) and T 13 (phobia syndrome), and the accuracy rate is over 99%.
Non-invasive prenatal DNA testing is also called non-invasive prenatal DNA testing and non-invasive fetal chromosome aneuploidy testing. According to the Committee of American College of Obstetrics and Gynecology, an international authoritative academic organization, non-invasive prenatal examination is the most widely used technical name. Non-invasive DNA prenatal detection technology only needs to extract the venous blood of pregnant women, and use the new generation DNA sequencing technology to sequence the free DNA fragments (including fetal free DNA) in pregnant women's peripheral plasma, and analyze the biological information of the sequencing results to obtain the genetic information of the fetus, so as to detect whether the fetus has three major chromosome diseases. Maternal plasma contains fetal free DNA, which provides a practical basis for this project. Fetal chromosome abnormality will bring DN to mother.
A content changes slightly, which can be detected by deep sequencing and bioinformatics analysis, providing theoretical basis for the project.
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