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:
Apr. 21, 2025

Filed:

Jun. 27, 2023
Applicant:

Alida Biosciences, Inc., San Diego, CA (US);

Inventors:

Gudrun Stengel, San Diego, CA (US);

Hua Yu, San Diego, CA (US);

Andrew Price, San Diego, CA (US);

Jerome Santos, San Diego, CA (US);

Yu-Hsien Hwang-Fu, San Diego, CA (US);

Byron Purse, San Diego, CA (US);

Assignee:

ALIDA BIOSCIENCES, INC., San Diego, CA (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C12Q 1/6883 (2017.12); C12N 9/22 (2005.12); C12N 15/10 (2005.12); C12Q 1/48 (2005.12); C12Q 1/6806 (2017.12); C12Q 1/6853 (2017.12); C12Q 1/6874 (2017.12);
U.S. Cl.
CPC ...
C12Q 1/6883 (2012.12); C12N 9/22 (2012.12); C12N 15/1065 (2012.12); C12Q 1/485 (2012.12); C12Q 1/6806 (2012.12); C12Q 1/6853 (2012.12); C12Q 1/6874 (2012.12);
Abstract

Provided herein are compositions and methods for the multiplexed profiling of RNA and DNA modifications across transcriptomes and genomes, respectively. The methods combine molecular recognition of non-canonical features (e.g., base modifications, backbone modifications, lesions, and/or structural elements) of a target nucleic acid with a step of writing the information from this recognition event into the neighboring genetic sequence of the target nucleic acid using a barcode. The resultant barcoded nucleic acids are then converted into sequencing libraries and read by DNA/RNA sequencing methods. This step reveals the sequence of the barcode, which is correlated with the non-canonical feature in the target nucleic acid(s). The high throughput profiling methods described herein allow for identification and/or localization of one or more modifications in a target nucleic acid. The methods also allow for identification of the nature and location of several or all DNA/RNA modifications in parallel.


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