Macro-gene library building method of nanopore sequencing platform and kit thereof
A nanopore sequencing and kit technology, applied in the field of sequencing, can solve the problems of time-consuming, inability to meet the needs of simple and fast infection detection process, etc.
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Embodiment 1
[0105] Embodiment 1 performance optimization and parameter adjustment experiment
[0106] The present invention uses ONT's PCR barcode kit (SQK-PBK004) as the basis for optimization experiments.
[0107] The present invention first selected a DNA nucleic acid standard product ZymoBIOMICS produced by Zymo Research Company TM Microbial Community DNA Standard (CatalogNos.D6305) is used as the input for verification. It is composed of 8 kinds of bacteria and 2 kinds of fungi that are clinically very common in precise quantitative proportions. The overall GC content is widely distributed (15%-85%, as follows Table, DNA Standard Composition (Catalog Nos.D6305 (Zymo Research, Product Manual)). It is a good standard for studying microbiome.
[0108] Table 1. ZymoBIOMICS TM Microbial Community DNA Standard strain information
[0109]
[0110] 1) Optimal screening of end repair and ligase
[0111] Considering the high requirements for sample size, experimental accuracy, and time...
Embodiment 2
[0124] Embodiment 2 establishes the method system of the present invention
[0125] Based on the optimization experiment in Example 1, the library construction method system of the present invention was obtained, and the method system was based on the PCR barcode kit (SQK-PBK004) of ONT.
[0126] 1. End repair of DNA fragments
[0127] 1 Add the finishing system to the 0.2mL PCR tube:
[0128]
[0129] Note: The total amount of sample extraction is supplemented with 100ng, and 45μL is put into it.
[0130] 2 Gently blow and mix with a pipette (do not shake and mix), collect the reaction solution to the bottom of the tube after a short centrifugation, and place the PCR tube on the PCR machine for the following reactions:
[0131] temperature time 20℃ 10min 65℃ 10min
[0132] 2. Joint connection:
[0133] 1 After the reaction is over, add the adapter connection system to the PCR tube:
[0134]
[0135] 2 Mix by blowing with a pipette, place...
Embodiment 3
[0161] The preparation of embodiment 3 kits
[0162] According to the process system determined in Example 2, we assembled this protocol into two library preparation kits as shown in the table below. In view of the difference in storage temperature of the kits, we prepared them into two packaged kits, which need to be stored separately. Under the conditions of -20℃±5℃ and 2~8℃.
[0163] Kit 1 contains the following components (stored at -20°C±5°C):
[0164]
[0165]
[0166] Kit 2 contains the following components (stored at 2-8°C):
[0167]
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