Nucleic acid sequencing system

Patent metadata

Field	Value
Publication number	US-12497657-B2
Application number	US-202519200289-A
Country	US
Kind code	B2
Filing date	May 6, 2025
Priority date	Jan 26, 2007
Publication date	Dec 16, 2025
Grant date	Dec 16, 2025

Abstract

A system for sequencing nucleic acid comprising a plurality of stations and a system control. The system control configured to direct the first substrate to progress and retrogress between the first processing station and the imaging station, direct the second substrate to progress and retrogress between the second processing station and the imaging station, and direct a chemistry cycle of a first sequencing procedure to occur within one of the first processing station or the second processing station while an imaging cycle of a second sequencing procedure occurs within the imaging station.

First claim

What is claimed is:

1 . A system for sequencing nucleic acids over a plurality of chemistry and imaging cycles, the system comprising:
a plurality of stages comprising a first stage and a second stage, wherein the first stage comprises one or more first vacuum lines for removal of first reagents from a first substrate, and wherein the second stage comprises one or more second vacuum lines for removal of second reagents from a second substrate; a plurality of stations comprising: an insert station configured to allow the first substrate and the second substrate to be inserted into and removed from a system; a plurality of fluidics stations configured to fluidically communicate with reagent reservoirs, the plurality of fluidics stations comprising: (i) a first fluidics station comprising a dispensing nozzle configured to deliver the first reagents to the first substrate and (ii) a second fluidics station comprising a dispensing nozzle configured to deliver the second reagents to the second substrate; and an imaging station comprising an objective configured to collect signals indicative of nucleotides present at nucleic acid sites on the first substrate and the second substrate, respectively; and a system control configured to: direct the first substrate to move back and forth between the first fluidics station and the imaging station, direct the second substrate to move back and forth between the second fluidics station and the imaging station, and direct a chemistry cycle of a first sequencing procedure to occur within one of the first fluidics station or the second fluidics station while an imaging cycle of a second sequencing procedure occurs within the imaging station.

2 . The system of claim 1 , wherein the system is configured such that a third substrate can be added to or removed from the insert station without interrupting the imaging cycle occurring within the imaging station.

3 . The system of claim 1 , further comprising the first substrate and the second substrate, wherein each of the first substrate and the second substrate comprises a flow cell.

4 . The system of claim 3 , further comprising the reagent reservoirs, wherein the reagent reservoirs contain reagents comprising a polymerase and one or more types of nucleotides.

5 . The system of claim 4 , wherein the system control is further configured to monitor a level of the reagents in the reservoirs.

6 . The system of claim 1 , wherein the objective is part of an optical system comprising at least one light source and at least one image sensor.

7 . The system of claim 6 , wherein the at least one image sensor is configured to optically image fluorescence of fluorescent tags at the nucleic acid sites.

8 . The system of claim 7 , wherein the at least one light source comprises one or more lasers configured to excite the fluorescent tags.

9 . The system of claim 1 , wherein the system control is further configured to:
monitor a system parameter, and end at least one of the sequencing procedures.

10 . The system of claim 1 , wherein the system control is further configured to monitor sample quality.

11 . The system of claim 1 , wherein the system control is further configured to re-focus at least one of the first substrate or the second substrate within the imaging station.

12 . The system of claim 1 , wherein the objective is part of a detection system comprising at least one laser light source and at least one imaging sensor, the detection system configured to direct radiation from the at least one laser light source to the nucleic acid sites at an exposure level, and
wherein the system control is configured to automatically modify the detection system to increase the exposure level of the radiation directed to the nucleic acid sites to an increased exposure level.

13 . The system of claim 12 , wherein the increase of the exposure level comprises at least one of an increase of a power output of the at least one laser light source or an increase of a time of exposure of the nucleic acid sites to the radiation.

14 . The system of claim 12 , wherein the system control is further configured to:
evaluate a decay in signal-to-noise ratio of fluorescence emission from the nucleic acid sites, and increase the exposure level based upon the decay in signal-to-noise ratio.

15 . A system for sequencing nucleic acids over a plurality of chemistry and imaging cycles, the system comprising:
a plurality of stages comprising a first stage and a second stage, wherein the first stage comprising one or more first vacuum lines for removal of first reagents from a first substrate, and wherein the second stage comprises one or more second vacuum lines for removal of second reagents from a second substrate; a plurality of stations comprising: an insert station comprising an access panel openable to receive at least one of the first substrate or the second substrate; a plurality of fluidics stations configured to fluidically communicate with reagent reservoirs, the plurality of fluidics stations comprising: (i) a first fluidics station configured to deliver the first reagents to the first substrate, and (ii) a second fluidics station configured to deliver the second reagents to the second substrate, wherein the second substrate is supported by a second stage comprising one of more second vacuum lines for removal of the reagents from the second substrate; and an imaging station comprising an objective configured to collect signals indicative of nucleotides present at nucleic acid sites on the first substrate and the second substrate, respectively; and a system control configured to: direct the first substrate to move back and forth between the first fluidics station and the imaging station, direct the second substrate to move back and forth between the second fluidics station and the imaging station, and direct a chemistry cycle of a first sequencing procedure to occur within one of the first fluidics station or the second fluidics station while an imaging cycle of a second sequencing procedure occurs within the imaging station.

16 . The system of claim 15 , wherein the one or more first vacuum lines are actuated by a first valve, and
wherein the one or more second vacuum lines are actuated by a second valve.

17 . The system of claim 15 , wherein the first stage comprises a first tray coupled to the one or more first vacuum lines, and
wherein the second stage comprises a second tray coupled to the one or more second vacuum lines.

18 . The system of claim 17 , wherein the one or more first vacuum lines are actuated by a first valve, and
wherein the one or more second vacuum lines are actuated by a second valve.

19 . The system of claim 15 , wherein the objective is part of a detection system comprising at least one light source and at least one image sensor.

20 . The system of claim 19 , wherein the detection system has a Rayleigh resolution between 0.2 μm and 10 μm.

21 . The system of claim 15 , wherein the system control is further configured to monitor data quality during the first sequencing procedure and the second sequencing procedure.

22 . A system for sequencing nucleic acids over a plurality of chemistry and imaging cycles, the system comprising:
a plurality of stages comprising a first stage and a second stage, wherein the first stage comprising a first tray coupled to one or more first vacuum lines for removal of first reagents from a first substr

Assignees

• Illumina Inc

Inventors

• Kain Robert C
• Heiner David L
• Zhao Chanfeng
• Gunderson Kevin

Classifications

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• C12Q1/686

  Polymerase chain reaction [PCR] · CPC title

• C12Q1/6874 Primary

  involving nucleic acid arrays, e.g. sequencing by hybridisation · CPC title