Three-generation library building sequencing method for whole genome full-length amplification based on novel coronavirus

A whole-genome and virus technology, applied in the field of third-generation library construction and sequencing, can solve the problems of not fully exploiting the advantages of long-read lengths, and not studying long-read length sequences, so as to reduce waste, prevent amplification bias, and improve experimental efficiency. Effect

Inactive Publication Date: 2020-09-04
WUHAN FRASERGEN CO LTD
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] However, at present, the accuracy of PCR amplification technology for the new coronavirus gene sequence needs to be improved, and the long-read advantage of PacBio's third-generation sequencing has not been fully utilized. No research has been done on the basis of PacBio third-generation sequencing to obtain more than 99% of long-read sequences, which can be used for virus mutation detection, assembly, traceability analysis, etc.

Method used

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  • Three-generation library building sequencing method for whole genome full-length amplification based on novel coronavirus
  • Three-generation library building sequencing method for whole genome full-length amplification based on novel coronavirus
  • Three-generation library building sequencing method for whole genome full-length amplification based on novel coronavirus

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Embodiment 1

[0044] 1. Primer design and synthesis

[0045] Searching for the new coronavirus on NCBI, a total of 74 new coronavirus sequences were downloaded and obtained. By checking the sequence integrity and deleting sequences with a length of less than 20k, a total of 43 complete new coronavirus sequences were obtained. All 43 complete genome sequences were compared to obtain a consensus sequence, and the consensus sequence of the new coronavirus genome is shown in SEQ ID NO: 1.

[0046] Based on the consensus sequence, a total of 30 pairs of primers were designed. The primers covered the entire 2019-nCoV genome. The primer positions were designed based on the conserved regions of the genome. There was an overlap of about 100 bp between each pair of primers. The size of the PCR product amplified by each pair of primers was 0.9-1.2 k. Primer design positions such asfigure 1 As shown, the primers in this scheme include a total of 30 pairs, and the amplified fragment size of each pair o...

Embodiment 2

[0081] Example 2: Comparison of virus data ratios in the amplified sequencing data

[0082] Table 6 shows the proportion of virus data in the sequencing data before and after the amplification of nucleic acid samples WD1 and WD2 extracted from oral swabs in Example 1.

[0083] Table 6:

[0084] sample name Unamplified Data Virus Ratio Amplified Data Virus Ratio Increase multiple WD1 0.7622% 71.20% 93.4 WD2 0.0014% 13.79% 9850

[0085] It can be seen that, after the sample is amplified by improving the amplification method provided by the present invention, the data virus ratio is increased to hundreds of times to hundreds of thousands of times, and the virus information can be enriched, which greatly reduces the sequencing data. waste.

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Abstract

The invention discloses a three-generation library building sequencing method for whole genome full-length amplification based on novel coronavirus. The three-generation library building sequencing method comprises the following steps of 1) designing and synthesizing primers according to a novel coronavirus genome consistency sequence; 2) carrying out full-length amplification on the genome of thenovel coronavirus; 3) performing mixing on the whole genome amplicon samples; 4) performing library construction; and 5) performing third-generation sequencing. According to the method, the odd primers and the even primers are combined to respectively amplify, and the odd amplification fragments and the even amplification fragments are mixed so as to obtain the amplicon fragment covering the whole novel coronavirus genome, such that only two amplification reactions are required, and the experiment efficiency is substantially improved. In addition, through the PacBio library building process,sequencing connectors with barcodes are added to the two ends of an amplicon, PacBio sequencing can be carried out, and HiFiReads with the accuracy rate being 99% or above are obtained after splittingand data correction.

Description

technical field [0001] The invention relates to the technical field of gene sequencing, in particular to a three-generation library construction and sequencing method based on the full-length amplification of the whole genome of the new coronavirus. Background technique [0002] The new coronavirus is an enveloped, non-segmented positive-sense single-stranded RNA virus with round or oval particles and a diameter of about 80-120 nm. The virus particle is wrapped by the lipid bilayer provided by the host cell, which contains nucleic acid and nucleocapsid protein. There are three main proteins: envelope protein (E protein), membrane protein (M protein) and spike protein (S protein). . The length of each genome of this virus is about 30,000 nucleotides. The gene sequence shows that SARS-CoV-2 belongs to a virus with a long branch in the evolutionary tree of the Betacoronavirus Lineage β (Sarbecovirus), which is similar to that of the Chinese Coronaviruses found in horseshoe ba...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/70C12Q1/6869C12Q1/6806C40B50/06C12R1/93
CPCC12Q1/701C12Q1/6869C12Q1/6806C40B50/06C12Q2600/172
Inventor 方涛
Owner WUHAN FRASERGEN CO LTD
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