http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2020108387-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-00
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filingDate 2020-03-09^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9bfe33eb4a8c1a40831de2d7c4e8ae0
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publicationDate 2020-07-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2020108387-A
titleOfInvention Sequencing without enzymes and amplification
abstract PROBLEM TO BE SOLVED: To provide a sequencing probe, a method, a kit and a device which provide a nucleic acid sequencing method which has a long read length and a low error rate and which does not require enzyme, amplification and library. The invention relates to sequencing probes, methods, kits, and devices that provide enzyme-free, amplification-free, and library-free nucleic acid sequencing methods with long read lengths and low error rates. .. A sequencing probe comprising a target binding domain and a barcode domain is used, wherein said target binding domain comprises at least 4 nucleotides and is capable of binding a target nucleic acid, wherein said barcode domain Comprises a synthetic backbone, said barcode domain comprising at least one first attachment region, said first attachment region comprising a nucleic acid sequence capable of being bound by a first complementary nucleic acid molecule, wherein The nucleic acid sequence of the first attachment region determines the position and identity of the first nucleotide in the target nucleic acid bound by the first nucleotide of the target binding domain. [Selection diagram] Figure 1
priorityDate 2014-11-21^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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