Systems and methods for determining nucleic acids

Patent metadata

Field	Value
Publication number	US-12104151-B2
Application number	US-202318185048-A
Country	US
Kind code	B2
Filing date	Mar 16, 2023
Priority date	Jul 30, 2014
Publication date	Oct 1, 2024
Grant date	Oct 1, 2024

Abstract

The present invention generally relates to systems and methods for imaging or determining nucleic acids, for instance, within cells. In some embodiments, the transcriptome of a cell may be determined. Certain embodiments are directed to determining nucleic acids, such as mRNA, within cells at relatively high resolutions. In some embodiments, a plurality of nucleic acid probes may be applied to a sample, and their binding within the sample determined, e.g., using fluorescence, to determine locations of the nucleic acid probes within the sample. In some embodiments, codewords may be based on the binding of the plurality of nucleic acid probes, and in some cases, the codewords may define an error-correcting code to reduce or prevent misidentification of the nucleic acids. In certain cases, a relatively large number of different targets may be identified using a relatively small number of labels, e.g., by using various combinatorial approaches.

First claim

The invention claimed is:

1. A method of using a plurality of error-robust in-situ hybridization primary nucleic acid probe pools to reduce misidentification of a plurality of distinct RNA species in a sample, comprising:
a. contacting the sample comprising the plurality of distinct RNA species in situ with the primary nucleic acid probe pools each of the nucleic acid probes comprising a target sequence and one or more read sequences, wherein each pool hybridizes to a distinct RNA species and each pool of probes encode a N-bit codeword with a Hamming weight of at least 4 that was assigned to each distinct RNA species, wherein each assigned N-bit codeword is a valid codeword with a Hamming distance equal to or greater than 4 between valid codewords wherein each of the read sequences correspond to a bit value of 1 for the codeword assigned to the distinct RNA species;
b. contacting the bound primary nucleic acid probes with a plurality of readout probes comprising a fluorescent label, wherein the readout probes hybridize to the read sequences of the primary nucleic probes;
c. imaging the readout probes bound to the primary nucleic acid probes; and,
d. repeating steps b) and c) in one or more sequential hybridization and imaging rounds until all N positions in the N-bit codeword have been imaged providing an imaged error-robust codeword reducing misidentification for the plurality distinct RNA species.

2. The method of claim 1 , wherein the RNA species is a RNA transcript.

3. The method of claim 1 , comprising determining the spatial organization of a transcriptome from a single cell.

4. The method of claim 1 , wherein each primary nucleic acid probe pool comprises at least 10 different primary nucleic acid probes.

5. The method of claim 1 , wherein each primary nucleic acid probe pool comprises at least four distinct read sequences.

6. The method of claim 1 , wherein each primary nucleic acid probe pool comprises four distinct read sequences.

7. The method of claim 1 , wherein each primary nucleic acid probe comprises two read sequences and one target sequence.

8. The method of claim 1 , wherein each primary nucleic acid probe pool comprises at least eight distinct read sequences.

9. The method of claim 1 , wherein the target sequence comprises an average length of between 10 and 200 nucleotides.

10. The method of claim 1 , wherein each primary nucleic acid probe pool comprises at least 10 different target sequences.

11. The method of claim 1 , wherein after each hybridization and imaging round the fluorescent label is quenched to inactivate.

12. The method of claim 1 , wherein after each hybridization and imaging round the fluorescent label is inactivated by chemically or enzymatically cleaving the fluorescent label from the readout probe.

13. The method of claim 1 , wherein the N-bit codeword comprises at least a 16-bit code.

14. The method of claim 1 , wherein the plurality of readout probes comprise at least two distinct fluorescent labels.

15. The method of claim 1 , wherein the plurality of readout probes comprise at least three distinct fluorescent labels.

16. The method of claim 1 , wherein the spatial organization of the distinct RNA species is imaged in 2 dimensions.

17. The method of claim 1 , wherein the spatial organization of the distinct RNA species is imaged in 3 dimensions.

18. The method of claim 1 , comprising determining abundance of the distinct RNA species.

19. A method for determining a plurality of nucleic acid targets within a sample by in situ hybridization, comprising:
(a) contacting a sample comprising a plurality of nucleic acid targets with a plurality of primary nucleic acid probes, wherein each primary nucleic acid probe comprises (i) a target sequence and (ii) one or more read sequences, wherein the target sequence hybridizes to the nucleic acid target in the sample to form a primary probe-hybridized complex;
(b) contacting the sample to a second round of hybridization using a plurality of secondary nucleic acid probes wherein the secondary nucleic acid probes comprise a first portion that hybridizes to a subset of the read sequences of the primary nucleic acid probe and a second portion comprising a fluorescent label to form a secondary probe-hybridized complex;
(c) detecting a fluorescent signal from each of the secondary probe-hybridized complexes;
(d) removing the secondary nucleic acid probes or inactivating the fluorescent signal from each of the secondary probe-hybridized complexes; and
(e) repeating steps (b) through (d) with multiple sets of differing secondary nucleic acid probes to generate a pattern of binding of the secondary nucleic acid probes;
wherein the pattern of binding of the secondary nucleic acid probes is converted to a codeword, wherein the codeword determines the identity of the nucleic acid target, and wherein the codeword facilitates error correction.

20. The method of claim 19 , wherein the target sequence of the plurality of primary nucleic acid probes comprises an average length of between 10 and 195 nucleotides.

21. The method of claim 19 , wherein the nucleic acid target is RNA.

22. The method of claim 21 , wherein the method comprises determining the transcriptome of a cell.

23. The method of claim 22 , wherein at least 25% of the transcriptome is determined.

24. The method of claim 19 , wherein the plurality of primary nucleic acid probes comprises at least 10 different primary nucleic acid probes.

25. The method of claim 19 , wherein the codeword comprises N-positions and wherein less than all possible codewords are used to identify the plurality of nucleic acid targets.

26. The method of claim 19 , wherein each set of the plurality of secondary nucleic acid probes hybridizes to a subset of the read sequences.

27. The method of claim 19 , wherein the one or more read sequences have an average length of at least 15 nucleotides.

28. The method of claim 19 , wherein the fluorescent signal is inactivated by photobleaching.

29. The method of claim 19 , wherein the fluorescent signal is inactivated by removal of the secondary nucleic acid probe from the readout probe-hybridized complexes or by chemically or enzymatically cleaving the fluorescent label from the readout probe-hybridized complexes.

30. The method of claim 19 , wherein the fluorescent signal is detected using a fluorescence imaging technique.

31. The method of claim 19 , wherein the one or more read sequences are distributed on the plurality of primary nucleic acid probes so as to define an error-correcting code.

32. The method of claim 19 , wherein if the pattern of binding of the secondary nucleic acid probes identifies a codeword that does not match a valid codeword, error correction is applied to the codeword to form a valid codeword.

33. The method of claim 19 , wherein the error correction system comprises a Hamming system, a Golay code, a SECDED (single error correction, double error detection) system or an extended Hamming system.

34. The method of claim 19 , wherein the error correction identifies the location of an error.

35. The method of claim 19 , wherein the error correction identifies a single bit error.

36. The method of claim 19 , wherein the error corr

Assignees

• Harvard College

Inventors

• Zhuang Xiaowei
• Chen Kok-Hao
• Boettiger Alistair
• Moffitt Jeffrey R
• Wang Siyuan

Classifications

• C12Q1/6837

  using probe arrays or probe chips (C12Q1/6874 takes precedence) · CPC title

• G16C20/10

  Analysis or design of chemical reactions, syntheses or processes · CPC title

• G06N7/01

  Probabilistic graphical models, e.g. probabilistic networks · CPC title

• G16B40/10

  Signal processing, e.g. from mass spectrometry [MS] or from PCR · CPC title

• G16B25/20

  Polymerase chain reaction [PCR]; Primer or probe design; Probe optimisation · CPC title