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US Patent 10954548 Nuclease profiling system

Patent 10954548 was granted and assigned to President and Fellows of Harvard College on March, 2021 by the United States Patent and Trademark Office.

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Is a
Patent
Patent
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Patent attributes

Patent Applicant
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President and Fellows of Harvard College
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Current Assignee
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President and Fellows of Harvard College
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Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
109545480
Patent Inventor Names
David R. Liu0
Vikram Pattanayak0
Date of Patent
March 23, 2021
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Patent Application Number
149111170
Date Filed
August 8, 2014
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Patent Citations
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US Patent 10077453 CAS9 proteins including ligand-dependent inteins
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US Patent 10113163 Adenosine nucleobase editors and uses thereof
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US Patent 10227581 Engineered transcription activator-like effector (TALE) domains and uses thereof
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US Patent 10167457 Nucleobase editors and uses thereof
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US Patent 10323236 Evaluation and improvement of nuclease cleavage specificity
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US Patent 10465176 Cas variants for gene editing
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US Patent 10508298 Methods for identifying a target site of a CAS9 nuclease
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US Patent 10597679 Switchable Cas9 nucleases and uses thereof
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Patent Citations Received
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US Patent 12084663 Incorporation of unnatural amino acids into proteins using base editing
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US Patent 11542509 Incorporation of unnatural amino acids into proteins using base editing
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US Patent 11560566 Aptazyme-embedded guide RNAs for use with CRISPR-Cas9 in genome editing and transcriptional activation
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US Patent 11578343 CAS9 proteins including ligand-dependent inteins
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US Patent 11932884 High efficiency base editors comprising Gam
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US Patent 11999947 Adenosine nucleobase editors and uses thereof
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US Patent 12006520 Evaluation and improvement of nuclease cleavage specificity
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0
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Patent Primary Examiner
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Aaron A Priest
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Patent abstract

Some aspects of this disclosure provide strategies, methods, and reagents for determining nuclease target site preferences and specificity of site-specific endonucleases. Some methods provided herein utilize a novel “one-cut” strategy for screening a library of concatemers comprising repeat units of candidate nuclease target sites and constant insert regions to identify library members that can been cut by a nuclease of interest via sequencing of an intact target site adjacent and identical to a cut target site. Some aspects of this disclosure provide strategies, methods, and reagents for selecting a site-specific endonuclease based on determining its target site preferences and specificity. Methods and reagents for determining target site preference and specificity are also provided.

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