The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 14, 2022

Filed:

Sep. 13, 2017
Applicant:

Inivata Ltd., Cambridge, GB;

Inventors:

Samuel Woodhouse, Cambridge, GB;

Tim Forshew, Stevenage, GB;

Stefanie Viola Lensing, Cambridge, GB;

Assignee:

INIVATA LTD., Cambridge, GB;

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/6855 (2018.01); C12Q 1/6806 (2018.01); C12Q 1/6869 (2018.01); C12Q 1/68 (2018.01);
U.S. Cl.
CPC ...
C12Q 1/6855 (2013.01); C12Q 1/68 (2013.01); C12Q 1/6806 (2013.01); C12Q 1/6869 (2013.01); C12Q 2525/117 (2013.01); C12Q 2525/155 (2013.01); C12Q 2525/179 (2013.01); C12Q 2525/186 (2013.01); C12Q 2525/191 (2013.01); C12Q 2525/301 (2013.01); C12Q 2535/122 (2013.01); C12Q 2563/179 (2013.01);
Abstract

The invention relates to methods for labelling individual nucleic acid molecules present in a sample, comprising contacting the nucleic acid molecules with an adaptor or mixture of adaptors, wherein the adaptor or adaptors comprise one or more universal nucleotide bases and a ligation moiety at their 3' end, and ligating an adaptor to the nucleic acid of interest, wherein the adaptor is ligated to the nucleic acid molecules at the 3′ end of the adaptor. A random tag is then generated in situ by conducting an extension reaction over the ligated adaptor. Methods of the invention may be used to detect genetic alterations or variants in any nucleic acid with high specificity and high sensitivity, including mutations in nucleic acids such as ctDNA, cfDNA, and in viral, microbiome and plant nucleic acids. Methods of the invention may also be used in detection and correction of errors introduced into nucleic acids during processing.


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