Combinatorial decoding of random nucleic acid arrays
US-9163283-B2 · Oct 20, 2015 · US
US12297488B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12297488-B2 |
| Application number | US-202418972148-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 6, 2024 |
| Priority date | Apr 5, 2010 |
| Publication date | May 13, 2025 |
| Grant date | May 13, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention provides assays and assay systems for use in spatially encoded biological assays. The invention provides an assay system comprising an assay capable of high levels of multiplexing where reagents are provided to a biological sample in defined spatial patterns; instrumentation capable of controlled delivery of reagents according to the spatial patterns; and a decoding scheme providing a readout that is digital in nature.
Opening claim text (preview).
The invention claimed is: 1. A method for determining a presence of a nucleic acid at a location in a tissue section comprising: (a) contacting the tissue section with a substrate comprising a plurality of features, wherein a feature of the plurality of features comprises a capture agent, wherein the capture agent comprises: (i) a first sequence that binds the nucleic acid, and (ii) a second sequence comprising a coding tag, wherein a sequence of the coding tag corresponds to a location of the capture agent on the substrate; (b) determining the sequence of the coding tag, or a complement thereof, and all or a portion of the sequence of the nucleic acid bound to the capture agent, or a complement thereof; and (c) visualizing a spatial location of the nucleic acid in the tissue section corresponding to the determined sequence. 2. The method of claim 1 , wherein the capture agent is directly immobilized on the substrate. 3. The method of claim 1 , wherein the capture agent is indirectly immobilized on the substrate. 4. The method of claim 1 , wherein the capture agent is immobilized in a well on the substrate. 5. The method of claim 1 , wherein the substrate is incorporated into a flow cell. 6. The method of claim 1 , wherein the substrate is incorporated onto a slide. 7. The method of claim 1 , wherein the determining comprises sequencing. 8. The method of claim 1 , wherein the nucleic acid is DNA. 9. The method of claim 1 , wherein the nucleic acid is RNA. 10. The method of claim 1 , wherein the plurality of features comprises wells. 11. The method of claim 1 , wherein the tissue section is a fresh frozen tissue section. 12. The method of claim 1 , wherein the tissue section is a formalin fixed paraffin embedded tissue section. 13. The method of claim 1 , wherein the method further comprises staining the tissue section. 14. The method of claim 1 , wherein the method further comprises imaging the tissue section. 15. The method of claim 1 , wherein the substrate comprises greater than 10,000 features. 16. The method of claim 1 , wherein the capture agent further comprises a primer binding site. 17. The method of claim 1 , wherein multiple tissue sections are contacted with the substrate. 18. The method of claim 1 , wherein the method further comprises determining the abundance of the nucleic acid in the tissue section. 19. The method of claim 1 , wherein the tissue section is permeabilized prior to step (b). 20. A method for spatial analysis comprising: (a) contacting a tissue section with a substrate of a flow cell, wherein the substrate comprises a plurality of wells, wherein a well of the plurality of wells comprises a capture agent immobilized therein, and wherein the capture agent comprises: (i) a first sequence that binds a nucleic acid of the tissue section, and (ii) a second sequence comprising a coding tag, wherein a sequence of the coding tag corresponds to a location of the capture agent on the substrate; wherein nucleic acids of the tissue section are bound to capture agents at locations of the substrate that correspond to locations of the nucleic acids in the tissue section; (b) determining the sequence of the coding tag, or a complement thereof, and all or a portion of the sequence of the nucleic acid bound to the capture agent, or a complement thereof; and (c) visualizing a spatial location of the nucleic acids in the tissue section corresponding to the determined sequences. 21. The method of claim 20 , wherein the capture agent is directly immobilized in the well of the substrate. 22. The method of claim 20 , wherein the capture agent is indirectly immobilized in the well of the substrate. 23. The method of claim 20 , wherein the determining comprises sequencing. 24. The method of claim 20 , wherein the nucleic acid is RNA. 25. The method of claim 20 , wherein the tissue section is a fresh frozen tissue section. 26. The method of claim 20 , wherein the method further comprises staining the tissue section. 27. The method of claim 20 , wherein the method further comprises imaging the tissue section. 28. The method of claim 20 , wherein the capture agent further comprises a primer binding site. 29. The method of claim 20 , wherein multiple tissue sections are contacted with the substrate. 30. The method of claim 20 , wherein the method further comprises determining the abundance of the nucleic acids in the tissue section.
Rare earth chelates · CPC title
Methods of protein analysis involving mass spectrometry · CPC title
Expression markers · CPC title
Polymorphic or mutational markers · CPC title
Allele-specific amplification · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.