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US Patent 11512308 Nucleic acid library methods

Patent 11512308 was granted and assigned to 10X Genomics on November, 2022 by the United States Patent and Trademark Office.

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Contents

Is a
Patent
Patent

Patent attributes

Patent Applicant
10X Genomics
10X Genomics
Current Assignee
10X Genomics
10X Genomics
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
11512308
Date of Patent
November 29, 2022
Patent Application Number
17690628
Date Filed
March 9, 2022
Patent Citations
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US Patent 10059990 In situ nucleic acid sequencing of expanded biological samples
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US Patent 10078895 Prediction of recurrence of non-small cell lung cancer with tumor infiltrating lymphocyte (TIL) graphs
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US Patent 10196691 Colon cancer gene expression signatures and methods of use
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US Patent 10208982 Airfoil blade and method of assembly
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US Patent 10221461 Immunocompetence assessment by adaptive immune receptor diversity and clonality characterization
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US Patent 10246752 Methods of monitoring conditions by sequence analysis
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US Patent 10273541 Methods and systems for processing polynucleotides
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US Patent 10472669 Spatially encoded biological assays
...
Patent Citations Received
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US Patent 12129516 Quantitative and automated permeabilization performance evaluation for spatial transcriptomics
0
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US Patent 11926863 Solid state single cell method for analyzing fixed biological cells
0
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US Patent 11926822 Three-dimensional spatial analysis
0
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US Patent 11965213 Methods of detecting spatial heterogeneity of a biological sample
0
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US Patent 11970739 Multiplex capture of gene and protein expression from a biological sample
0
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US Patent 11981958 Methods for spatial analysis using DNA capture
0
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US Patent 11981960 Spatial analysis utilizing degradable hydrogels
0
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US Patent 12060604 Spatial analysis of epigenetic modifications
0
...
Patent Primary Examiner
‌
David C Thomas
CPC Code
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C12Q 2525/191
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C12Q 2537/159
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C12Q 1/6837
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C12Q 2563/179
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C12N 15/1093
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C12Q 2539/101
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C12Q 1/6874
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C12Q 2525/131

Provided herein are methods, compositions, and kits for removing a portion of a sequence in a member of a nucleic acid library.

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