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US Patent 12024738 Methods for cancer detection and monitoring

Patent 12024738 was granted and assigned to Natera on July, 2024 by the United States Patent and Trademark Office.

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Patent
Patent
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Patent attributes

Patent Applicant
Natera
Natera
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Current Assignee
Natera
Natera
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Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
120247380
Patent Inventor Names
Ryan Swenerton0
Raheleh Salari0
Hsin-Ta Wu0
Himanshu Sethi0
Bernhard Zimmermann0
Date of Patent
July 2, 2024
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Patent Application Number
163825200
Date Filed
April 12, 2019
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Patent Citations
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US Patent 7035739 Computer systems and methods for identifying genes and determining pathways associated with traits
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US Patent 7058517 Methods for obtaining and using haplotype data
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US Patent 7058616 Method and system for predicting resistance of a disease to a therapeutic agent using a neural network
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US Patent 7101663 PCR method
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US Patent 7153656 Nucleic acid sequence detection using multiplexed oligonucleotide PCR
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US Patent 7218764 Ploidy classification method
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US Patent 7297485 Method for nucleic acid amplification that results in low amplification bias
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US Patent 7332277 Methods for detection of genetic disorders
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...
Patent Primary Examiner
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Carla J. Myers
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Patent abstract

The invention provides methods for detecting single nucleotide variants in breast cancer, bladder cancer, or colorectal cancer. Additional methods and compositions, such as reaction mixtures and solid supports comprising clonal populations of nucleic acids, are provided. For example, provided here is a method for monitoring and detection of early relapse or metastasis of breast cancer, bladder cancer, or colorectal cancer, comprising generating a set of amplicons by performing a multiplex amplification reaction on nucleic acids isolated from a sample of blood or urine or a fraction thereof from a patient who has been treated for a breast cancer, bladder cancer, or colorectal cancer, wherein each amplicon of the set of amplicons spans at least one single nucleotide variant locus of a set of patient-specific single nucleotide variant loci associated with the breast cancer, bladder cancer, or colorectal cancer; and determining the sequence of at least a segment of each amplicon of the set of amplicons that comprises a patient-specific single nucleotide variant locus, wherein detection of one or more patient-specific single nucleotide variants is indicative of early relapse or metastasis of breast cancer, bladder cancer, or colorectal cancer.

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