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US Patent 8697363 Methods for detecting multiple target nucleic acids in multiple samples by use nucleotide tags

Patent 8697363 was granted and assigned to Fluidigm Corporation on April, 2014 by the United States Patent and Trademark Office.

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Contents

Is a
Patent
Patent

Patent attributes

Current Assignee
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
8697363
Patent Inventor Names
Marc Unger0
Bernhard G. Zimmermann0
Ramesh Ramakrishnan0
Alain Mir0
Date of Patent
April 15, 2014
Patent Application Number
12548132
Date Filed
August 26, 2009
Patent Citations Received
‌
US Patent 12129512 Composition comprising cell origination barcodes for the analysis of both protein and nucleic acid from the same cell
0
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US Patent 11932903 Kit for split-pool barcoding target molecules that are in or on cells or cell organelles
0
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US Patent 11932902 Barcoded beads and method for making the same by split-pool synthesis
0
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US Patent 11939624 Method for labeling ligation products with cell-specific barcodes II
0
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US Patent 12018323 Nucleic acid encoding reactions
0
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US Patent 12065690 Methods of identifying multiple epitopes in cells
0
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US Patent 12110536 Methods of identifying multiple epitopes in cells
0
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US Patent 12129513 Method for barcoding
0
...
Patent Primary Examiner
‌
Christopher M Babic
Patent abstract

The present invention provides assay methods that increase the number of samples and/or target nucleic acids that can be analyzed in a single assay. In certain embodiments, an assay method entails separately subjecting S samples to an encoding reaction that produces a set of T tagged target nucleotide sequences, each tagged target nucleotide sequence including a sample-specific nucleotide tag and a target nucleotide sequence. In some embodiments, an assay method entails separately subjecting S samples to an encoding reaction that produces a set of T tagged target nucleotide sequences, each tagged target nucleotide sequence including a first nucleotide tag linked to a target nucleotide sequence, which is linked to a second nucleotide tag. In either case, the tagged target nucleotide sequences from the S samples can be mixed to form an assay mixture and subsequently assayed.

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