Patents by Inventor Stephanie C. HUELGA

Stephanie C. HUELGA 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).

  • Patent number: 10927405
    Abstract: Described herein are methods, compositions and kits for identifying modifications that could lead to false positive detections in nucleic acid sequencing. In some embodiments, the methods, compositions and kits provided herein are useful for reducing potential of false positive detection of variants caused by errors during sample preparation or sequencing.
    Type: Grant
    Filed: January 11, 2019
    Date of Patent: February 23, 2021
    Assignee: NUGEN TECHNOLOGIES, INC.
    Inventors: Douglas A. Amorese, Stephanie C. Huelga, Bin Li
  • Publication number: 20190144928
    Abstract: Described herein are methods, compositions and kits for identifying modifications that could lead to false positive detections in nucleic acid sequencing. In some embodiments, the methods, compositions and kits provided herein are useful for reducing potential of false positive detection of variants caused by errors during sample preparation or sequencing.
    Type: Application
    Filed: January 11, 2019
    Publication date: May 16, 2019
    Inventors: Douglas A. Amorese, Stephanie C. Huelga, Bin Li
  • Patent number: 10190155
    Abstract: Described herein are methods, compositions and kits for identifying modifications that could lead to false positive detections in nucleic acid sequencing. In some embodiments, the methods, compositions and kits provided herein are useful for reducing potential of false positive detection of variants caused by errors during sample preparation or sequencing.
    Type: Grant
    Filed: October 14, 2016
    Date of Patent: January 29, 2019
    Assignee: NuGEN Technologies, Inc.
    Inventors: Douglas A. Amorese, Stephanie C. Huelga, Bin Li
  • Publication number: 20190005193
    Abstract: Disclosed herein are methods, compositions and kits for quantitating one or more specific nucleic acids within a plurality of nucleic acids. In some embodiments, a sequencing library is constructed from enriched probe extension products specific for the specific nucleic acids and sequenced. In some embodiments, the resulting reads are used for removing duplicate reads. In some embodiments, counting of verified probes is used to quantitate or determine the number of specific nucleic acid molecules in the starting nucleic acid sample.
    Type: Application
    Filed: September 7, 2018
    Publication date: January 3, 2019
    Inventors: Jonathan Scolnick, Benjamin G. Schroeder, Douglas A. Amorese, Stephanie C. Huelga
  • Patent number: 10102337
    Abstract: Disclosed herein are methods, compositions and kits for quantitating one or more specific nucleic acids within a plurality of nucleic acids. In some embodiments, a sequencing library is constructed from enriched probe extension products specific for the specific nucleic acids and sequenced. In some embodiments, the resulting reads are used for removing duplicate reads. In some embodiments, counting of verified probes is used to quantitate or determine the number of specific nucleic acid molecules in the starting nucleic acid sample.
    Type: Grant
    Filed: August 6, 2015
    Date of Patent: October 16, 2018
    Assignee: NuGEN Technologies, Inc.
    Inventors: Jonathan Scolnick, Benjamin Schroeder, Douglas Amorese, Stephanie C. Huelga
  • Publication number: 20180105870
    Abstract: Described herein are methods, compositions and kits for identifying modifications that could lead to false positive detections in nucleic acid sequencing. In some embodiments, the methods, compositions and kits provided herein are useful for reducing potential of false positive detection of variants caused by errors during sample preparation or sequencing.
    Type: Application
    Filed: October 14, 2016
    Publication date: April 19, 2018
    Inventors: Douglas A. Amorese, Stephanie C. Huelga, Bin Li
  • Publication number: 20160203259
    Abstract: Disclosed herein are methods, compositions and kits for quantitating one or more specific nucleic acids within a plurality of nucleic acids. In some embodiments, a sequencing library is constructed from enriched probe extension products specific for the specific nucleic acids and sequenced. In some embodiments, the resulting reads are used for removing duplicate reads. In some embodiments, counting of verified probes is used to quantitate or determine the number of specific nucleic acid molecules in the starting nucleic acid sample.
    Type: Application
    Filed: August 6, 2015
    Publication date: July 14, 2016
    Inventors: Jonathan SCOLNICK, Benjamin SCHROEDER, Douglas AMORESE, Stephanie C. HUELGA