Patents by Inventor Taylor Jacob Jensen

Taylor Jacob Jensen has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Systems for non-invasive assessment of chromosome alterations using changes in subsequence mappability
    Patent number: 11929146
    Abstract: Provided herein are methods, processes, systems, machines and apparatuses for non-invasive assessment of chromosome alterations.
    Type: Grant
    Filed: August 19, 2019
    Date of Patent: March 12, 2024
    Assignee: SEQUENOM, INC.
    Inventors: Sung Kim, Taylor Jacob Jensen, Mathias Ehrich
  • Methods and Processes for Non-Invasive Assessment of Genetic Variations
    Publication number: 20220411871
    Abstract: Technology provided herein relates in part to methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Application
    Filed: May 23, 2022
    Publication date: December 29, 2022
    Applicant: Sequenom, Inc.
    Inventors: Taylor Jacob Jensen, Jennifer Geis, Sung Kyun Kim, Cosmin Deciu, Mathias Ehrich
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS
    Publication number: 20220403468
    Abstract: Technology provided herein relates in part to methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Application
    Filed: June 8, 2021
    Publication date: December 22, 2022
    Applicant: SEQUENOM, INC.
    Inventors: Taylor Jacob JENSEN, Mathias EHRICH
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS
    Publication number: 20220383977
    Abstract: Provided herein are methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Application
    Filed: August 2, 2022
    Publication date: December 1, 2022
    Inventors: Cosmin DECIU, Zeljko DZAKULA, Mathias EHRICH, Taylor Jacob JENSEN
  • Methods and processes for non-invasive detection of a microduplication or a microdeletion with reduced sequence read count error
    Patent number: 11437121
    Abstract: Provided herein are methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Grant
    Filed: April 23, 2018
    Date of Patent: September 6, 2022
    Assignee: Sequenom, Inc.
    Inventors: Cosmin Deciu, Zeljko Dzakula, Mathias Ehrich, Taylor Jacob Jensen
  • Methods and processes for non-invasive assessment of genetic variations
    Patent number: 11365447
    Abstract: Technology provided herein relates in part to methods, processes and apparatuses for non-invasive assessment of genetic variations. In particular the invention relates to methods and kits for detecting aneuploidy of a fetal chromosome by determining the amounts of differentially methylated regions in each of chromosomes 13, 18 and 21 in circulating cell-free nucleic acid from a human pregnant female.
    Type: Grant
    Filed: March 12, 2015
    Date of Patent: June 21, 2022
    Assignee: Sequenom, Inc.
    Inventors: Taylor Jacob Jensen, Jennifer Geis, Sung Kyun Kim, Cosmin Deciu, Mathias Ehrich
  • Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus
    Patent number: 11060145
    Abstract: Technology provided herein relates in part to methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Grant
    Filed: March 13, 2014
    Date of Patent: July 13, 2021
    Assignee: Sequenom, Inc.
    Inventors: Taylor Jacob Jensen, Mathias Ehrich
  • Processes and Compositions for Methylation-Based Enrichment of Fetal Nucleic Acid From a Maternal Sample Useful for Non-Invasive Prenatal Diagnoses
    Publication number: 20200208212
    Abstract: Provided are compositions and processes that utilize genomic regions that are differentially methylated between a mother and her fetus to separate, isolate or enrich fetal nucleic acid from a maternal sample. The compositions and processes described herein are particularly useful for non-invasive prenatal diagnostics, including the detection of chromosomal aneuploidies.
    Type: Application
    Filed: March 17, 2020
    Publication date: July 2, 2020
    Applicant: Sequenom, Inc.
    Inventors: Mathias Ehrich, Anders Olof Herman Nygren, Taylor Jacob Jensen
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF CHROMOSOME ALTERATIONS
    Publication number: 20200058372
    Abstract: Provided herein are methods, processes, systems, machines and apparatuses for non-invasive assessment of chromosome alterations.
    Type: Application
    Filed: August 19, 2019
    Publication date: February 20, 2020
    Applicant: SEQUENOM, INC.
    Inventors: Sung KIM, Taylor Jacob JENSEN, Mathias EHRICH
  • Non-invasive assessment of chromosome alterations using change in subsequence mappability
    Patent number: 10438691
    Abstract: Provided herein are methods, processes, systems, machines and apparatuses for non-invasive assessment of chromosome alterations.
    Type: Grant
    Filed: October 3, 2014
    Date of Patent: October 8, 2019
    Assignee: SEQUENOM, INC.
    Inventors: Sung Kim, Taylor Jacob Jensen, Mathias Ehrich
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS
    Publication number: 20190005188
    Abstract: Provided herein are methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Application
    Filed: April 23, 2018
    Publication date: January 3, 2019
    Inventors: COSMIN DECIU, Zeljko DZAKULA, Mathias EHRICH, Taylor Jacob JENSEN
  • Reducing sequence read count error in assessment of complex genetic variations
    Patent number: 9984198
    Abstract: Provided herein are methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Grant
    Filed: March 12, 2013
    Date of Patent: May 29, 2018
    Assignee: SEQUENOM, INC.
    Inventors: Cosmin Deciu, Zeljko Dzakula, Mathias Ehrich, Taylor Jacob Jensen
  • Methods for Detecting Genetic Variations
    Publication number: 20170342477
    Abstract: Technology provided herein relates in part to methods, processes, machines and apparatuses for detecting genetic variations. In some embodiments, the technology is related to non-invasive assessment of aneuploidies.
    Type: Application
    Filed: May 26, 2017
    Publication date: November 30, 2017
    Applicant: Sequenom, Inc.
    Inventors: Taylor Jacob Jensen, Mathias Ehrich, Dirk van den Boom, John Allen Tynan, Sung Kyun Kim, Timothy S. Burcham, Christopher K. Ellison, Youting Sun
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS
    Publication number: 20170073756
    Abstract: Technology provided herein relates in part to methods, processes and apparatuses for non-invasive assessment of genetic variations. In particular the invention relates to methods and kits for detecting aneuploidy of a fetal chromosome by determining the amounts of differentially methylated regions in each of chromosomes 13, 18 and 21 in circulating cell-free nucleic acid from a human pregnant female.
    Type: Application
    Filed: March 12, 2015
    Publication date: March 16, 2017
    Inventors: Taylor Jacob JENSEN, Jennifer GEIS, Sung Kyun KIM, Cosmin DECIU, Mathias EHRICH
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF CHROMOSOME ALTERATIONS
    Publication number: 20160292356
    Abstract: Provided herein are methods, processes, systems, machines and apparatuses for non-invasive assessment of chromosome alterations.
    Type: Application
    Filed: October 3, 2014
    Publication date: October 6, 2016
    Inventors: Sung KIM, Taylor Jacob JENSEN, Mathias EHRICH
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS
    Publication number: 20160145685
    Abstract: Technology provided herein relates in part to methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Application
    Filed: March 13, 2014
    Publication date: May 26, 2016
    Inventors: Taylor Jacob JENSEN, Mathias EHRICH
  • Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non invasive prenatal diagnoses
    Patent number: 8962247
    Abstract: Provided are compositions and processes that utilize genomic regions that are differentially methylated between a mother and her fetus to separate, isolate or enrich fetal nucleic acid from a maternal sample. The compositions and processes described herein are particularly useful for non-invasive prenatal diagnostics, including the detection of chromosomal aneuplodies.
    Type: Grant
    Filed: March 18, 2010
    Date of Patent: February 24, 2015
    Assignee: Sequenom, Inc.
    Inventors: Mathias Ehrich, Anders Olof Herman Nygren, Taylor Jacob Jensen
  • METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS
    Publication number: 20130325360
    Abstract: Provided herein are methods, processes and apparatuses for non-invasive assessment of genetic variations.
    Type: Application
    Filed: March 12, 2013
    Publication date: December 5, 2013
    Applicant: SEQUENOM, INC.
    Inventors: COSMIN DECIU, Zeljko Dzakula, Mathias Ehrich, Taylor Jacob Jensen