According to different places, different regions and different hospitals, the charging standards are different. It is recommended to go to the local hospital for relevant consultation.
The price mainly depends on your requirements and what kind of project you want to do. Take natural genes as an example. If you don't graduate from biomedical major, you may choose cheap, hundreds of dollars each, and test one or several genes. This is obviously not good.
Talent is a complex thing, which is determined by many factors and genes. It's hard to imagine that a gene determines a certain talent. Of course, this is not what you want. Of course you want to spend money and help you. Right?
I suggest you choose Xue Jiajin's products. Xue Jiajin can be detected by complex genetic testing items of oral mucosa. Xue Jia's genetic testing projects include the decoding of gifted genes, 36 tumor risk genes, 150 major diseases, 150 common diseases, infertility genes, perfect baby genes, molecular typing genes of tumors and common diseases, and 100 drug guidance genes. These are not expensive, ranging from 3000 yuan to tens of thousands of yuan. In addition, it is more scientific to charge for good learning genes mainly according to the complexity of the genes analyzed and evaluated.
Non-invasive costs are affected by many aspects and cannot be generalized. Non-invasive costs are mainly affected by the following aspects:
First, the influence of hospital level: it is different to do inspections in advanced hospitals and ordinary hospitals. High-level hospitals are relatively better than ordinary hospitals in transportation, environment, medical equipment and doctors, and of course the fees charged are relatively high.
Second, the influence of the region: Different places will naturally have different inspection fees due to different economic levels and consumption levels.
Third, the influence of pregnant women's own situation: people's constitutions are different. Some pregnant women may have to check some other aspects when doing non-invasive because of their own physical reasons, so the cost will be higher than that of ordinary pregnant women.
The specification clearly stipulates that there are three main types of pregnant women who are suitable for non-invasive DNA prenatal testing:
1. In the prenatal screening report, the detection values of down syndrome risk rate are ≤ 1/270,11000 ≤18-trisomy syndrome ≤65438.
2. Contraindications for interventional prenatal diagnosis such as threatened abortion, fever, bleeding tendency and unhealed infection during pregnancy.
3. Being in the first trimester (more than 20 weeks +6 days), and just within the time for non-invasive DNA prenatal testing, I missed the time for serological screening or the opportunity for prenatal diagnosis, but I have special requirements for reducing the risk of three chromosomal diseases.
Compared with the applicable population, the effect of non-invasive DNA prenatal testing will be reduced to some extent. Beware of pregnant women:
1, prenatal screening for pregnant women over 35 years old with high risk and expected delivery age, and other direct prenatal diagnosis indications.
2. Pregnant with twins.
3. gestational age
4. weight >; 100 kg.
5. In vitro fertilization-embryo transfer pregnancy.
6. Suffering from malignant tumor.
Extended data
Gene detection
Gene is the basic unit of heredity. By copying the DNA or RNA sequence carrying genetic information to the next generation, it can guide the synthesis of protein to express its own genetic information, thus controlling the expression of individual traits.
Genetic testing is a technique to detect DNA through blood, other body fluids or cells. It is a method to take the peripheral venous blood or other tissue cells of the subject, amplify their genetic information, and then detect the DNA molecular information in the cells of the subject through special equipment, and analyze whether the gene type, gene defect and expression function are normal, so as to make people know their own genetic information, clarify the cause or predict the risk of a certain disease.
Genetic testing can be used to diagnose diseases and predict the risk of diseases. Disease diagnosis is the use of gene detection technology to detect mutant genes that cause hereditary diseases. At present, the most widely used genetic testing is the detection of neonatal hereditary diseases, the diagnosis of hereditary diseases and the auxiliary diagnosis of some common diseases.
Baidu Encyclopedia: Genetic Testing