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US Patent 11920192 Single nucleotide detection method and associated probes

Patent 11920192 was granted and assigned to Lightcast Discovery on March, 2024 by the United States Patent and Trademark Office.

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Patent abstractTimelineTable: Further ResourcesReferences
Is a
Patent
Patent
1

Patent attributes

Patent Applicant
Lightcast Discovery
Lightcast Discovery
1
Current Assignee
Lightcast Discovery
Lightcast Discovery
1
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
1
Patent Number
119201921
Patent Inventor Names
Barnaby Balmforth1
Mark Dethlefsen1
Cameron Alexander Frayling1
Date of Patent
March 5, 2024
1
Patent Application Number
166135931
Date Filed
May 15, 2018
1
Patent Citations
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US Patent 9856528 Single nucleotide detection method
1
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US Patent 9771615 Sequencing method
1
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US Patent 10000802 Sequencing method
1
Patent Primary Examiner
Young J. Kim
Young J. Kim
1
CPC Code
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C12Q 1/6869
1
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C12Q 2525/307
1
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C12Q 2563/107
1
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C12Q 2563/159
1
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C12Q 2521/307
1
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C12Q 2525/125
1
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C12Q 1/6823
1
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C12Q 2521/101
1
...
Patent abstract

A method of sequencing a nucleic acid comprising (1) generating a stream of single nucleoside triphosphates by progressive enzymatic digestion of the nucleic acid; (2) producing at least one oligonucleotide used probe by reacting, in the presence of a polymerase, at least one of the single nucleoside triphosphates with a corresponding biological probe comprising (a) a first single-stranded oligonucleotide including an exonuclease blocking-site, a restriction endonuclease recognition-site located on the 5′ side of the blocking-site and including a single nucleotide capture-site e, and at least one fluorophore region and (b) a second and optionally a third single-stranded oligonucleotide each separate from the first oligonucleotide; (3) cleaving the first oligonucleotide strand of the used probe at the recognition-site with a restriction endonuclease; (4) digesting the first oligonucleotide component with an enzyme to yield fluorophores in a detectable state and (5) detecting the fluorophores released in step (4).

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