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:
Aug. 20, 2024

Filed:

May. 10, 2021
Applicant:

Life Technologies Corporation, Carlsbad, CA (US);

Inventors:

Mark Andersen, Carlsbad, CA (US);

Daniel Mazur, San Diego, CA (US);

Sihong Chen, Vista, CA (US);

Guobin Luo, Oceanside, CA (US);

Xinzhan Peng, San Diego, CA (US);

Assignee:

Life Technologies Corporation, Carlsbad, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12N 15/10 (2006.01); C12Q 1/6806 (2018.01); C12Q 1/6853 (2018.01); C12Q 1/6855 (2018.01); C12Q 1/686 (2018.01); C40B 40/06 (2006.01); C40B 20/04 (2006.01); C40B 50/06 (2006.01);
U.S. Cl.
CPC ...
C12N 15/1068 (2013.01); C12N 15/1065 (2013.01); C12Q 1/6806 (2013.01); C12Q 1/6853 (2013.01); C12Q 1/6855 (2013.01); C12Q 1/686 (2013.01); C40B 20/04 (2013.01); C40B 40/06 (2013.01); C40B 50/06 (2013.01);
Abstract

Provided are methods for preparing a library of target nucleic acid sequences, as well as compositions and uses therefor. Methods comprise contacting a nucleic acid sample with a plurality of adaptors capable of amplification of one or more target nucleic acid sequences under conditions wherein the target nucleic acid(s) undergo a first amplification; digesting the resulting first amplification products; repairing the digested target amplicons; and amplifying the repaired products in a second amplification, thereby producing a library of target nucleic acid sequence. Each of the plurality of adaptor compositions comprise a handle and a targeted nucleic acid sequence and optionally one or more tag sequences. Provided methods may be carried out in a single, addition only workflow reaction, allowing for rapid production of highly multiplexed targeted libraries, optionally including unique tag sequences. Resulting library compositions are useful for a variety of applications, including sequencing applications.


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