A novel coronavirus whole genome capture method, primer set and kit
A coronavirus and genome technology, applied in biochemical equipment and methods, recombinant DNA technology, microbial measurement/inspection, etc., can solve the problem that new coronaviruses cannot achieve large-scale promotion, rapid diagnosis, and long detection time (requires 24- 72 hours, it is not easy to obtain the whole genome information and other issues, to achieve the effects of sequencing economy, reducing the risk of cross contamination, and low sample quality requirements
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Embodiment 1
[0035] Example 1 Based on the ultra-sensitive novel coronavirus genome capture method for library construction and sequencing
[0036] The present invention specifically uses multiplex PCR technology to perform targeted amplification on the gene sequence of SARS-CoV-2, which improves the sequencing depth, effectively reduces the cost of subsequent sequencing and shortens the research time. A key point of multiplex PCR technology is to design a reasonable multiplex PCR primer pair combination, ensure that there are no overlapping amplicons in the primer combination, and reduce the interaction between primers. This method designs 98 pairs of primers, and uses the Invitrogen SurSprit III ONE-STEP RT-PCR amplification system to take a small amount of RNA and quickly amplify the whole genome of the coronavirus. After the amplification reaction is completed, the PCR reaction will be obtained Coronavirus gene fragments of different sizes can be directly used on the computer for secon...
Embodiment 2
[0066] Example 2 Comparison of the ultrasensitive novel coronavirus whole genome capture method of the present invention with other methods
[0067] The capture method of the present invention can not only amplify samples with high virus content such as virus strains, but also samples with relatively low virus content such as throat swabs and sputum. All genome sequences can be amplified.
[0068] The ultrasensitive novel coronavirus whole genome capture method of the present invention is compared with other existing methods, as shown in Table 2. The results show that the existing methods such as direct RNA library construction method and direct library construction after reverse transcription cannot obtain the whole genome sequence well, and the operation time of the capture method after library construction and the direct RNA library construction method is relatively short compared with the present invention. Longer, although the reverse transcription library construction m...
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