IPC분류정보
국가/구분 |
United States(US) Patent
등록
|
국제특허분류(IPC7판) |
|
출원번호 |
UP-0644255
(2009-12-22)
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등록번호 |
US-7843567
(2011-01-31)
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발명자
/ 주소 |
- Moon, John A.
- Kersey, Alan D.
- Putnam, Martin A.
- Li, Tuo
|
출원인 / 주소 |
|
대리인 / 주소 |
The Small Patent Law Group
|
인용정보 |
피인용 횟수 :
16 인용 특허 :
338 |
초록
▼
A method of identifying an analyte. The method includes providing a plurality of microparticles. The microparticles have optically detectable codes extending along bodies of the corresponding microparticle. The microparticles have the chemical probes attached thereto. Each of the chemical probes is
A method of identifying an analyte. The method includes providing a plurality of microparticles. The microparticles have optically detectable codes extending along bodies of the corresponding microparticle. The microparticles have the chemical probes attached thereto. Each of the chemical probes is associated with a corresponding one of the codes. The method also includes selectively binding target analytes to the chemical probes on the microparticles to produce labeled microparticles and distributing the labeled microparticles to random locations of a substrate. The method also includes determining the codes for the labeled microparticles in the random array and code positions of the codes in the random array. The method further includes detecting the label on the labeled microparticles in the random array and label positions of the labels in the random array. The method also includes using the code positions and the label positions to analyze the target analyte.
대표청구항
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What is claimed is: 1. A method of identifying an analyte, the method comprising: providing a plurality of microparticles, the microparticles having elongated bodies with optically detectable codes extending along the bodies of the corresponding microparticles, the microparticles having chemical pr
What is claimed is: 1. A method of identifying an analyte, the method comprising: providing a plurality of microparticles, the microparticles having elongated bodies with optically detectable codes extending along the bodies of the corresponding microparticles, the microparticles having chemical probes attached thereto, each of the chemical probes being associated with a corresponding one of the codes; selectively binding target analytes to the chemical probes on the microparticles to produce labeled microparticles; distributing the labeled microparticles to random locations of a substrate, thereby providing a random array of labeled microparticles; determining the codes for the labeled microparticles in the random array and code positions of the codes in the random array; detecting labels on the labeled microparticles in the random array and label positions of the labels in the random array; and using the code positions and the label positions to analyze the target analytes. 2. The method of claim 1, wherein the chemical probes and the target analytes comprise nucleic acids. 3. The method of claim 2, wherein the method comprises determining a genotype. 4. The method of claim 2, wherein the method comprises gene expression analysis. 5. The method of claim 1, wherein the code determining and label detecting operations are conducted in an automated manner. 6. The method of claim 1, wherein the labels are fluorescent labels and the label detecting operation includes capturing at least one image of fluorescent optical output emanating from the microparticles on the substrate. 7. The method of claim 1, wherein the code determining operation includes capturing at least one image of an optical output indicative of the codes for the microparticles. 8. The method of claim 7, wherein the optical output includes one of light reflected by the codes and light transmitted through the codes. 9. The method of claim 1, wherein the distributing the labeled microparticles onto the substrate includes flowing the microparticles onto the substrate within a solution, the microparticles falling onto the substrate in a random distribution. 10. The method of claim 9, wherein the code determining operation includes illuminating the microparticles on the substrate while submerged within the solution. 11. The method of claim 10, wherein the microparticles comprise a material having a refractive index and the solution has a refractive index, the material of the microparticles and the solution being substantially index-matched. 12. The method of claim 1, wherein the code determining operation includes illuminating the particles with an incident light, the incident light being substantially perpendicular to a plane of the substrate. 13. The method of claim 1, wherein the substrate is a two-dimensional substrate, the microparticles being arranged co-planar with each other. 14. The method of claim 1, wherein the substrate includes a plurality of grooves, the method further comprising orienting the elongated bodies of the microparticles within the grooves, the microparticles being randomly distributed within the grooves. 15. The method of claim 1, wherein the microparticles are rectangular and have a substantially square cross-sectional shape. 16. The method of claim 1, wherein the microparticles have an inner region and an outer region that surrounds the inner region, the inner region extending along a longitudinal axis of the microparticles and being located at a center of the microparticles, the code being within the inner region. 17. The method of claim 1, wherein the code is completely surrounded by a transparent material and extends along a longitudinal axis of the microparticle such that the code is determinable from any direction about the longitudinal axis. 18. The method of claim 1, wherein the code comprises a grating having a periodic or aperiodic variation in at least one of a refractive index and an optical absorption of at least a portion of the microparticle. 19. The method of claim 1, wherein the code is one of written, impressed, embedded, imprinted, etched, grown, and deposited within the microparticle. 20. A method of nucleic acid analysis, the method comprising: providing a plurality of microparticles, the microparticles having elongated bodies with optically detectable codes extending along the bodies of the corresponding microparticles, the microparticles having nucleic acid probes attached thereto, each of the nucleic acid probes being associated with a corresponding one of the codes; hybridizing target nucleic acids to complementary nucleic acid probes on the microparticles to produce labeled microparticles; distributing the labeled microparticles to random locations of a substrate, thereby providing a random array of labeled microparticles; determining the codes for the labeled microparticles in the random array and code positions of the codes in the random array; detecting labels on the labeled microparticles in the random array and label positions of the labels in the random array; and using the code positions and the label positions to analyze the target nucleic acids. 21. The method of claim 20, wherein the method comprises determining a genotype. 22. The method of claim 20, wherein the method comprises gene expression analysis. 23. The method of claim 20, wherein the code determining and label detecting operations are conducted in an automated manner. 24. The method of claim 20, wherein the labels are fluorescent labels and the label detecting operation includes capturing at least one image of fluorescent optical output emanating from the microparticles on the substrate. 25. The method of claim 20, wherein the code determining operation includes capturing at least one image of an optical output indicative of the codes for the microparticles. 26. The method of claim 25, wherein the optical output includes one of light reflected by the codes and light transmitted through the codes. 27. The method of claim 20, wherein the distributing the labeled microparticles onto the substrate includes flowing the microparticles onto the substrate within a solution, the microparticles falling onto the substrate in a random distribution. 28. The method of claim 20, wherein the code determining operation includes illuminating the microparticles on the substrate while submerged within a solution. 29. The method of claim 28, wherein the microparticles comprise a material having a refractive index and the solution has a refractive index, the material of the microparticles and the solution being substantially index-matched. 30. The method of claim 20, wherein the code determining operation includes illuminating the particles with an incident light, the incident light being substantially perpendicular to a plane of the substrate. 31. The method of claim 20, wherein the substrate is a two-dimensional substrate, the microparticles being arranged co-planar with each other. 32. The method of claim 20, wherein the substrate includes a plurality of grooves, the method further comprising orienting the elongated bodies of the microparticles within the grooves, the microparticles being randomly distributed within the grooves. 33. The method of claim 20, wherein the microparticles are rectangular and have a substantially square cross-sectional shape. 34. The method of claim 20, wherein the microparticles have an inner region and an outer region that surrounds the inner region, the inner region extending along a longitudinal axis of the microparticles and being located at a center of the microparticles, the code being within the inner region. 35. The method of claim 20, wherein the code is completely surrounded by a transparent material and extends along a longitudinal axis of the microparticle such that the code is determinable from any direction about the longitudinal axis. 36. The method of claim 20, wherein the code comprises a grating having a periodic or aperiodic variation in at least one of a refractive index and an optical absorption of at least a portion of the microparticle. 37. The method of claim 20, wherein the code is one of written, impressed, embedded, imprinted, etched, grown, and deposited within the microparticle. 38. The method of claim 20, further comprising determining the labels and determining the label positions. 39. The method of claim 20, wherein the code determining and label detecting operations comprise: (a) the determining the codes for the labeled microparticles in the random array; (b) the determining the code positions of the codes in the random array; (c) the detecting labels on the labeled microparticles in the random array; and (d) the detecting label positions of the labels in the random array; and wherein the operations of (a)-(d) occur in any order or simultaneously. 40. The method of claim 20, wherein the label detecting operation includes capturing at least one image of the labeled microparticles in the random positions on the substrate. 41. The method of claim 20 further comprising capturing at least one image of the labeled microparticles in the random positions on the substrate, wherein the at least one image is utilized during at least one of the code determining and label detecting operations. 42. The method of claim 20, wherein the target nucleic acids include nucleic acids of a common sequence. 43. The method of claim 20, wherein the target nucleic acids include at least first and second types of target nucleic acids, the first and second types of target nucleic acids having different nucleic acid sequences, the labels including at least first and second labels, the first and second labels being different and being associated with the first and second types of target nucleic acids, respectively. 44. The method of claim 1, further comprising determining the labels and determining the label positions. 45. The method of claim 1, wherein the code determining and label detecting operations comprise: (a) the determining the codes for the labeled microparticles in the random array; (b) the determining the code positions of the codes in the random array; (c) the detecting labels on the labeled microparticles in the random array; and (d) the detecting label positions of the labels in the random array; and wherein the operations of (a)-(d) occur in any order or simultaneously. 46. The method of claim 1, wherein the label detecting operation includes capturing at least one image of the labeled microparticles in the random positions on the substrate. 47. The method of claim 1 further comprising capturing at least one image of the labeled microparticles in the random positions on the substrate, wherein the at least one image is utilized during at least one of the code determining and label detecting operations. 48. The method of claim 1, wherein the target analytes include one type of target analyte. 49. The method of claim 1, wherein the target analytes include at least first and second types of target analytes, the first and second types of target analytes having different chemical structures, the labels including at least first and second labels, the first and second labels being different and being associated with the first and second types of target analytes, respectively.
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