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US Patent 11339429 Methods for non-invasive prenatal ploidy calling

Patent 11339429 was granted and assigned to Natera on May, 2022 by the United States Patent and Trademark Office.

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Is a
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
113394290
Patent Inventor Names
Allison Ryan0
Johan Baner0
Matthew Hill0
Matthew Rabinowitz0
Milena Banjevic0
Styrmir Sigurjonsson0
Zachary Demko0
George Gemelos0
...
Date of Patent
May 24, 2022
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Patent Application Number
164117700
Date Filed
May 14, 2019
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Patent Citations
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US Patent 10174369 Methods for non-invasive prenatal ploidy calling
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US Patent 10179937 Detecting mutations and ploidy in chromosomal segments
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US Patent 10227652 System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals
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US Patent 10017810 Methods for determining a nucleotide sequence contiguous to a known target nucleotide sequence
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US Patent 10041127 Systems and methods to detect rare mutations and copy number variation
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US Patent 10061890 Methods for non-invasive prenatal ploidy calling
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US Patent 10081839 System and method for cleaning noisy genetic data and determining chromosome copy number
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US Patent 10083273 System and method for cleaning noisy genetic data and determining chromosome copy number
...
Patent Primary Examiner
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Angela M Bertagna
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CPC Code
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C12Q 1/6827
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C12Q 2537/143
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C12Q 2600/156
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C12Q 1/6806
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C12Q 1/686
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C12Q 1/6874
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C12Q 1/6869
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C12Q 1/6883
0

The present disclosure provides methods for determining the ploidy status of a chromosome in a gestating fetus from genotypic data measured from a mixed sample of DNA comprising DNA from both the mother of the fetus and from the fetus, and optionally from genotypic data from the mother and father. The ploidy state is determined by using a joint distribution model to create a plurality of expected allele distributions for different possible fetal ploidy states given the parental genotypic data, and comparing the expected allelic distributions to the pattern of measured allelic distributions measured in the mixed sample, and choosing the ploidy state whose expected allelic distribution pattern most closely matches the observed allelic distribution pattern. The mixed sample of DNA may be preferentially enriched at a plurality of polymorphic loci in a way that minimizes the allelic bias, for example using massively multiplexed targeted PCR.

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