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filingDate 2018-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d740c8b182f6d3d9635f2d601e82beca
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publicationDate 2020-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110904512-A
titleOfInvention A high-throughput sequencing library construction method suitable for single-stranded DNA
abstract The invention discloses a high-throughput sequencing library construction method suitable for single-stranded DNA. The method of the present invention comprises: connecting a single-stranded template with a double-stranded linker 1 with a degenerate base (a special linker with a degenerate base makes it possible to connect the single-stranded template with the double-stranded linker, and the double-stranded linker can be randomly Bind to the single-stranded template, make the linker sequence sufficiently close to the template, and then use T4 DNA ligase to complete the connection); use the extension primer to extend to obtain a double-stranded product; connect the double-stranded product with the linker 2; The obtained ligation product is Template, PCR amplification was performed to obtain the desired library. The present invention can be used to construct high-throughput sequencing libraries, and can also be used to construct single-stranded DNA libraries. The present invention will improve the utilization rate of single-stranded DNA in the construction of high-throughput sequencing libraries, and further realize the purpose of building libraries with low starting amount. In the future It plays a key role in early tumor screening and prognostic monitoring applications.
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