Granted Patent B2

US 12,545,955 · App. 17/852,192 · Granted Feb 10, 2026

Inventors: Stuart William Reid (Oxford, GB); Gavin Harper (Oxford, GB); Clive Gavin Brown (Oxford, GB); Daniel John Turner (Oxford, GB); Andrew John Heron (Oxford, GB); Christopher James Wright (Oxford, GB)

Assignee: Oxford Nanopore Technologies PLC

C12Q1/6869G01N33/48721G16B30/00G16B30/10

Abstract

Claims (47)

1 . A method of controlling a biochemical analysis system, the method comprising:

analyzing a series of measurements obtained from a portion of a first polymer that is partially translocated through a nanopore of the biochemical analysis system, and reference data derived from at least one reference sequence of polymer units, wherein the first polymer is a polynucleotide, and the series of measurements is obtained from around 30 nucleotides or greater of the first polymer;

providing a measure of similarity during translocation between the analyzed series of measurements and the reference data; and

operating the biochemical analysis system to eject the first polymer from the nanopore responsive to the measure of similarity.

2 . The method of claim 1 , wherein the biochemical analysis system comprises at least one sensor element that comprises the nanopore, wherein the at least one sensor element is operable to eject the first polymer that is translocating through the nanopore, and the step of operating the biochemical analysis system to eject the first polymer comprises operating the sensor element to eject the first polymer from the nanopore and accept a further polymer in the nanopore.

3 . The method of claim 2 , wherein the at least one sensor element is operable to eject the first polymer by application of an ejection bias voltage sufficient to eject the first polymer, the step of operating the sensor element to eject the first polymer from the nanopore is performed by applying an ejection bias voltage and the step of operating the sensor element to accept the further polymer in the nanopore is performed by applying a translocation bias voltage sufficient to enable translocation of the further polymer therethrough.

4 . The method of claim 1 , wherein the biochemical analysis system comprises an array of sensor elements and is operable to take successive measurements of the first polymer from sensor elements selected in a multiplexed manner, and the step of operating the biochemical analysis system to eject the first polymer comprises operating the biochemical analysis system to cease taking measurements from the currently selected sensor element and to start taking measurements from a newly selected sensor element.

5 . The method of claim 4 , wherein the measurements comprise electrical measurements taken from the sensor elements and the biochemical analysis system is operable to take successive measurements of the first polymer from sensor elements selected in an electrically multiplexed manner.

6 . The method of claim 5 , wherein the biochemical analysis system comprises:

a detection circuit comprising a plurality of detection channels each capable of taking electrical measurements from a sensor element, the number of sensor elements in the array being greater than the number of detection channels; and

a switch arrangement capable of selectively connecting the detection channels to respective sensor elements in a multiplexed manner.

7 . The method of claim 4 , wherein the sensor elements are controllable to eject the first polymer, and the method further comprises, when operating the biochemical analysis system to cease taking measurements from the currently selected sensor element, also controlling the currently selected sensor element to eject the first polymer and thereby make the nanopore available to receive the further polymer.

8 . The method of claim 1 , wherein the at least one reference sequence of polymer units from which the reference data is derived is an unwanted sequence, and said step of operation to eject is performed responsive to the measure of similarity indicating that the first polymer is the unwanted sequence.

9 . The method of claim 1 , wherein the at least one reference sequence of polymer units from which the reference data is derived is a target, and said step of operation to eject is performed responsive to the measure of similarity indicating that the first polymer is not the target.

10 . The method of claim 1 , wherein the at least one reference sequence of polymer units from which the reference data is derived is an already measured sequence of polymer units, and said step of operation to eject is performed responsive to the measure of similarity indicating that the first polymer is the already measured sequence of polymer units.

11 . The method according claim 1 , wherein the at least one reference sequence of polymer units from which the reference data is derived comprises plural targets, and said step of operation to eject is performed responsive to the measure of similarity indicating that the first polymer is one of the targets.

12 . The method according claim 1 , wherein the reference data derived from the at least one reference sequence of polymer units represents actual or simulated measurements taken by a biochemical analysis system, and

said step of analyzing the series of measurements comprises:

comparing the series of measurements with the reference data.

13 . The method of claim 1 , wherein the reference data derived from the at least one reference sequence of polymer units represents a feature vector of time-ordered features representing characteristics of the measurements taken by a biochemical analysis system, and said step of analyzing the series of measurements comprises:

deriving, from the series of measurements, a feature vector of time-ordered features representing characteristics of the measurements, and

comparing the derived feature vector with the reference data.

14 . The method of claim 1 , wherein

the reference data derived from the at least one reference sequence of polymer units represents the identity of the polymer units of the at least one reference sequence, and

said step of analyzing the series of measurements comprises:

analyzing the series of measurements to provide an estimate of the identity of the polymer units of the sequence of around 30 nucleotides or greater of the first polymer, and

comparing the estimate with the reference data to provide the measure of similarity.

15 . The method of claim 1 , wherein the nanopore is a biological pore.

16 . The method of claim 1 , wherein the translocation of said first polymer through the nanopore is performed in a ratcheted manner.

17 . The method of claim 1 , wherein the measurements comprise electrical measurements.

18 . The method of claim 1 , wherein the method comprises, analyzing a series of measurements taken from around 30 nucleotides or greater of the first polymer as the first polymer partially translocates through the nanopore, using the reference data derived from the at least one reference sequence of polymer units to provide the measure of similarity between the sequence of the around 30 nucleotides or greater of the first polymer and the at least one reference sequence.

19 . The method of claim 1 , wherein the first polymer is at least 5 kilobases long.

20 . The method of claim 19 , wherein the first polymer is at least 30 kilobases long.

21 . The method of claim 1 , further comprising determining a sequence of polynucleotides from the analyzed series of measurements wherein the measure of similarity is made between the determined sequence and the reference data.

22 . The method of claim 1 , further comprising obtaining the series of measurements from the first polymer during the partial translocation.

23 . The method of claim 1 , wherein the reference data is derived from plural reference sequences of polymer units.

24 . The method of claim 22 , wherein the series of measurements is obtained by taking successive measurements of the polymer as it translocates through the nanopore.

25 . The method of claim 24 , wherein the successive measurements comprise one or more groups of plural measurements that are dependent on a single k-mer without a priori knowledge of the number of measurements in each group.

26 . The method of claim 1 , wherein analyzing the series of measurements and the reference data to provide the measure of similarity comprises using a distance function to provide, as the measure of similarity, a measure of the distance between the series of measurements and the reference data.

27 . A computer-implemented method of controlling a biochemical analysis system, the method comprising the method of claim 1 .

28 . The method of claim 1 , wherein the series of measurements is a series of electrical measurements.

29 . The method of claim 1 , wherein the measurements are raw measurements, wherein the raw measurements are electrical measurements or optical measurements or a combination thereof.

30 . A biochemical analysis system configured to:

eject a first polymer from a nanopore responsive to a measure of similarity, provided during translocation, between:

(i) an analyzed series of measurements obtained from a portion of the first polymer that is partially translocated through the nanopore and

(ii) reference data derived from at least one reference sequence of polymer units;

wherein the first polymer is a polynucleotide, and the series of measurements is obtained from around 30 nucleotides or greater of the first polymer.

Assignments (2)

Priority Claims (3)

Continuity (3)

References Cited (234)