Granted Patent B2

US 12,606,861 · App. 18/488,255 · Granted Apr 21, 2026

Inventors: Andrea Marziali (North Vancouver, CA); Joel Pel (Vancouver, CA)

Assignee: NCAN GENOMICS, INC.

C12Q1/6827C12Q1/68C12Q1/6806C12Q1/6855C12Q1/686C12Q1/6869C12Q2521/501C12Q2525/161C12Q2525/191C12Q2531/113C12Q2535/122

Abstract

Claims (30)

1 . A method for of selectively ligating adapters to a target nucleic acid, the method comprising:

providing a first linked ligation adapter comprising a first adapter linked to a first probe complementary to a first portion that is internal to 5′ and 3′ ends of the target nucleic acid, wherein the first probe is linked to the first adapter by a first linker;

hybridizing the first probe to the target nucleic acid; and

ligating the first adapter to a first terminus of the target nucleic acid to produce a first ligation product.

2 . The method of claim 1 , further comprising:

providing a second linked ligation adapter comprising a second adapter linked to a second probe complementary to a second portion of the target nucleic acid by a second linker;

hybridizing the second probe to the target nucleic acid; and

ligating the second adapter to a second terminus of the target nucleic acid to produce a second ligation product, wherein the first terminus and the second terminus are different ends of the target nucleic acid.

3 . The method of claim 2 , wherein the first probe and the second probe anneal to the target in one hybridization event, thereby promoting the ligation of the first adaptor and the second adaptor to their respective termini of the target nucleic acid.

4 . The method of claim 2 , wherein the first portion and the second portion are the same.

5 . The method of claim 1 , further comprising cleaving the first linker to separate the first probe from the first ligation product.

6 . The method of claim 5 , wherein the linker is cleaved by uracil digestion.

7 . The method of claim 1 , wherein the target nucleic acid is a fusion nucleic acid.

8 . The method of claim 1 , wherein the first adapter comprises one or more of a universal priming site, a unique molecular identifier, and a barcode.

9 . The method of claim 2 , wherein the second adapter comprises one or more of a universal priming site, a unique molecular identifier, and a barcode.

10 . The method of claim 1 , wherein the target nucleic acid has a length from about 100 nucleotides to about 500 nucleotides.

11 . The method of claim 1 , further comprising attaching copies of the first adapter to multiple different targets using multiple linked ligation adapters comprising different probes complementary to different target nucleic acid portions, each with the same first adapter.

12 . The method of claim 2 , further comprising attaching copies of the second adapter to multiple different targets using multiple second linked ligation adapters comprising different probes complementary to different target nucleic acid portions, each with the same second adapter.

13 . The method of claim 1 , wherein the first linked ligation adapter comprises a modified DNA base.

14 . The method of claim 2 , wherein the second linked ligation adapter comprises a modified DNA base.

15 . The method of claim 1 , wherein the first linked ligation adapter is blocked to prevent extension.

16 . The method of claim 2 , wherein the second linked ligation adapter is blocked to prevent extension.

17 . The method of claim 2 , further comprising amplifying the second ligation product.

18 . The method of claim 17 , wherein amplifying the second ligation product produces a library for sequencing.

19 . A method of enrichment of a target nucleic acid, the method comprising:

(a) producing a first mixture of ligation products by combining a mixture comprising nucleic acid fragments and a first linked ligation adapter comprising a first adapter linked to a first probe complementary to a first portion internal to 5′ and 3′ ends of the target nucleic acid, wherein the first adapter is linked to the first probe by a first linker;

(b) producing a second mixture of ligation products by combining a mixture comprising the first mixture and a second linked ligation adapter comprising a second adapter linked to a second probe complementary to a second portion of the target nucleic acid by a second linker; and

(c) removing fragments from the second mixture that are not ligated to the first or the second linked ligation adapters.

20 . The method of claim 19 , wherein the target nucleic acid is a fusion nucleic acid.

21 . The method of claim 19 , further comprising amplifying the second mixture after removing fragments not ligated to the first or the second linked ligation adapters.

Assignments (2)

Continuity (5)

References Cited (209)