Target species specific sequence acquisition method and target species detection method

A technology of target species and acquisition method, applied in sequence analysis, bioinformatics, informatics, etc., can solve the problems of high requirements, large amount of calculation, long time, etc., and achieve high reliability, high accuracy, and simple method Effect

Active Publication Date: 2021-02-05
成都基因坊科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This method has the following disadvantages: First, in order to ensure the comprehensiveness of the species as much as possible, the sequencing depth is high, the sequencing cost is high, and the subsequent assembly and analysis have high requirements on the computing platform, a large amount of calculation, and a long time. Unable to meet follow-up analysis requirements
Second, there may be homologous fragments between different species, and a metagenomic assembly fragment may have multiple different taxonomic statuses, which may cause uncertainty and affect the accuracy of species identification

Method used

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  • Target species specific sequence acquisition method and target species detection method
  • Target species specific sequence acquisition method and target species detection method

Examples

Experimental program
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Effect test

Embodiment 1

[0038] Toxoplasma identification:

[0039] Taking GCA_000006565.2 (Toxoplasma gondii ME49) as the reference genome, plus other genomes of Toxoplasma gondii (toxoplasma classification id--5811, 5 genomes), together as the whole genome sequence of Toxoplasma gondii, and by analyzing the Toxoplasma gondii Alignment of all the whole genome sequences, screening nucleic acid sequences with a sequence similarity of 100%, to obtain the core sequence of Toxoplasma gondii;

[0040]The cat genome (version 9) was used as the genome database of exogenous species, and all nucleic acid sequences of Toxoplasma gondii in NCBI's NT database were filtered out according to the classification number of Toxoplasma gondii. (This step first excludes the influence of cats (toxoplasma hosts) individuals, filters out a part of the core sequence of toxoplasma gondii, and improves the subsequent comparison efficiency with the NT nucleic acid sequence database; in addition, if there are more genomes of for...

Embodiment 2

[0045] The method for obtaining the specific sequence of Brucella canis (Brucella Canis), the method for obtaining the specific sequence of Brucella canis comprises the following steps:

[0046] Select the whole genome sequence of Brucella canis in the NCBI genome database, and by comparing the whole genome sequence of said Brucella canis, screen out the core sequence of Brucella canis; All the whole genome sequences of Rutella are compared, and the nucleic acid sequences with a sequence similarity of 100% are screened to obtain the core sequence of Brucella canis.

[0047] Filter out all nucleic acid sequences of the described Brucella canis (taxid--36855) in the NT nucleic acid database to obtain the non-Brucellus canis nucleic acid sequence database;

[0048] Taking Brucella melitensis, Brucellasuis, Brucellaovis, and canine genomes as exogenous species, first compare the core sequence of Brucella canis with the genome of the exogenous species, and filter out the nucleic ac...

Embodiment 3

[0051] The method for obtaining the unique sequence of canine parvovirus (Canine parvovirus), the method for obtaining the unique sequence of canine parvovirus comprises the following steps:

[0052] Select the whole genome sequence of canine parvovirus in the NCBI genome database, and screen out the core sequence of canine parvovirus by comparing the whole genome sequence of the canine parvovirus; wherein, all the whole genome sequences of the canine parvovirus According to the alignment, the nucleic acid sequences with a sequence similarity of 100% are screened to obtain the canine parvovirus core sequence.

[0053] Filter out all nucleic acid sequences of the canine parvovirus (classification id--10788) in the NT nucleic acid database to obtain a non-canine parvovirus nucleic acid sequence database;

[0054] Taking Chiropteranprotoparvovirus, Eulipotyphlaprotoparvovirus, and canine genome as exogenous species, first compare the canine parvovirus core sequence with the exoge...

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Abstract

The invention relates to a target species specific sequence acquisition method and a target species detection method; the target species specific sequence acquisition method comprises the following steps: selecting all whole genome sequences of a target species in a genome database, and screening out a target species core sequence by comparing all whole genome sequences of the target species; filtering out all nucleic acid sequences of the target species in a nucleic acid database to obtain a non-target species nucleic acid sequence database; and comparing the core sequence of the target species with a non-target species nucleic acid sequence database, and filtering out the nucleic acid sequence obtained by comparison in the core sequence of the target species to finally obtain a specificsequence of the target species. By means of the method, the specific sequence of the target species can be obtained, the method is simple and high in reliability, and the target species and the classification status of the organism can be determined by identifying whether the specific sequence of the target species exists in the sample or not. Therefore, the existence of the target species or theclassification status of the target species can be identified only by amplifying the specific sequence of the target species obtained by the method for obtaining the specific sequence of the target species.

Description

technical field [0001] The invention relates to the field of biotechnology, in particular to a method for obtaining a specific sequence of a target species and a method for detecting the target species. Background technique [0002] Traditional species identification methods include (1) identification of species based on 16s (bacteria), 18S (higher eukaryotes) or ITS (fungi) and key genes (viruses): by obtaining the DNA of the target species, performing PCR amplification, and performing Sanger For sequencing, submit the sequence to online blastn for sequence comparison. Based on sequence similarity, the taxonomic status of the species is determined. The detection efficiency of this detection method is low, and the DNA of a single species needs to be purified, and the taxonomic status of the species needs to be sequenced and compared; based on this method, the resolution is low, and many species cannot be determined, but can only be identified to the genus or family. (2) I...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G16B30/00
CPCG16B30/00
Inventor 陈艳朋邓操刘梦佳郝兆楠
Owner 成都基因坊科技有限公司
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