IP Library › Granted Patent US 10,557,133
Granted Patent B2
US 10,557,133 · App. 14/766,089 · Granted Feb 11, 2020

Methods and compositions for nucleic acid sequencing

Inventors: Frank J. Steemers (Encinitas, CA); Sasan Amini (Redwood City, CA); Kevin L. Gunderson (Encinitas, CA); Natasha Pignatelli (Berkeley, CA); Igor Goryshin (Madison, WI)
Assignee: ILLUMINA, INC.
C12N15/1065C12Q1/6806
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,557,133
App. No.
14/766,089
Granted
Feb 11, 2020
Kind
B2
Abstract

Embodiments of the present invention relate to sequencing nucleic acids. In particular, embodiments of the methods and compositions provided herein relate to preparing nucleic acid templates and obtaining sequence data therefrom.

Claims (12)

1. A method for preparing a library of template nucleic acids to obtain sequence information from a target nucleic acid, said method comprising:

(a) contacting a template nucleic acid with a plurality of transposomes to generate a tagmented template nucleic acid, wherein at least some of the transposomes each comprise a first transposon sequence, a second transposon sequence noncontiguous with said first transposon sequence, and a transposase associated with the first transposon sequence and the second transposon sequence, wherein a plurality of transposons are inserted into the target nucleic acid;

(b) compartmentalizing the tagmented template nucleic acid comprising said plurality of inserted transposons into each vessel of a plurality of vessels, wherein the compartmentalizing comprises distributing the tagmented template nucleic acid between the plurality of vessels to provide each vessel with an amount of tagmented template nucleic acid less than about one haploid equivalent of the target nucleic acid; and

(c) removing the transposase from the template nucleic acid.

2. The method of claim 1 , wherein step (c) comprises a method selected from the group consisting of adding a detergent, changing temperature, changing pH, adding a protease, adding a chaperone, and adding a polymerase.

3. The method of claim 1 , wherein the first transposon sequence comprises a first primer site and the second transposon sequences comprise a second primer site, wherein the first primer site further comprises a first barcode and the second primer site further comprises a second barcode.

4. The method of claim 3 , wherein the first barcode and second barcode are different.

5. The method of claim 1 , wherein step (a) further comprises enriching the template nucleic acid for a sequence of interest.

6. The method of claim 1 , further comprising obtaining sequence information from the template nucleic acid.

7. The method of claim 6 , wherein the sequence information comprises haplotype sequence information.

8. The method of claim 1 , wherein the template nucleic acid is from a single cell.

9. The method of claim 1 , wherein the template nucleic acid is total genomic DNA.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2015
From: STEEMERS, FRANK J.; AMINI, SASAN; GUNDERSON, KEVIN L.; PIGNATELLI, NATASHA; GORYSHIN, IGOR
To: ILLUMINA, INC.
Reel/Frame 037110/0505 →
Continuity (1)
Related Publication 20150368638A1 · Dec 24, 2015
Cited By (12)
US 12,195,786 US 12,227,793 US 12,247,247 US 12,247,248 US 12,252,734 US 12,252,735 US 12,252,736 US 12,252,737 US 12,305,219 US 12,305,220 US 12,305,221 US 12,570,971