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US Patent 10174369 Methods for non-invasive prenatal ploidy calling

Patent 10174369 was granted and assigned to Natera on January, 2019 by the United States Patent and Trademark Office.

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Contents

Is a
Patent
Patent

Patent attributes

Patent Applicant
Natera
Natera
Current Assignee
Natera
Natera
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
10174369
Date of Patent
January 8, 2019
Patent Application Number
15917383
Date Filed
March 9, 2018
Patent Citations Received
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US Patent 12110552 Methods for simultaneous amplification of target loci
0
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US Patent 11479812 Methods and compositions for determining ploidy
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US Patent 11482300 Methods for preparing a DNA fraction from a biological sample for analyzing genotypes of cell-free DNA
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US Patent 11485996 Methods for characterizing copy number variation using proximity-litigation sequencing
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US Patent 11486008 Detecting mutations and ploidy in chromosomal segments
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US Patent 12024738 Methods for cancer detection and monitoring
0
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US Patent 12084720 Assessing graft suitability for transplantation
0
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US Patent 11459615 Methods for simultaneous amplification of target loci
...
Patent Primary Examiner
‌
Larry D Riggs, II
Patent abstract

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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