Patents by Inventor Daniel M. Bornman

Daniel M. Bornman 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).

  • Publication number: 20230197196
    Abstract: In one illustrative embodiment, an allelotyping method may include selecting a plurality of text strings that each represent a nucleotide sequence that was read by a massively parallel sequencing (MPS) instrument, where the nucleotide sequences represented by the selected plurality of text strings each correspond to a particular locus, comparing the selected plurality of text strings to one another to determine an abundance count for each unique text string included in the selected plurality of text strings, and determining one or more alleles for the particular locus by comparing the abundance count for each unique text string included in the selected plurality of text strings to an abundance threshold.
    Type: Application
    Filed: October 11, 2022
    Publication date: June 22, 2023
    Inventors: Brian A. Young, Angela T. Minard-Smith, Esley M. Heizer, Jr., Daniel M. Bornman, Mark E. Hester, Boyu Yang
  • Patent number: 11475980
    Abstract: In at least one illustrative embodiment, a method may comprise selecting a first plurality of text strings that each represent a nucleotide sequence that was read by a massively parallel sequencing instrument, where the nucleotide sequences represented by the selected first plurality of text strings each correspond to a first target locus, comparing the selected first plurality of text strings to one another to determine an abundance count for each unique text string included in the selected first plurality of text strings, identifying a first number of unique text strings included in the selected first plurality of text strings as representing noise responses, and determining a method detection limit as a function of the abundance counts for the first number of unique text strings identified as representing noise responses.
    Type: Grant
    Filed: September 17, 2014
    Date of Patent: October 18, 2022
    Assignee: BATTELLE MEMORIAL INSTITUTE
    Inventors: Brian A. Young, Esley M. Heizer, Angela T. Minard-Smith, Nancy J. McMillan, Gokhan Yavas, Daniel M. Bornman
  • Patent number: 11468970
    Abstract: In one illustrative embodiment, an allelotyping method may include selecting a plurality of text strings that each represent a nucleotide sequence that was read by a massively parallel sequencing (MPS) instrument, where the nucleotide sequences represented by the selected plurality of text strings each correspond to a particular locus, comparing the selected plurality of text strings to one another to determine an abundance count for each unique text string included in the selected plurality of text strings, and determining one or more alleles for the particular locus by comparing the abundance count for each unique text string included in the selected plurality of text strings to an abundance threshold.
    Type: Grant
    Filed: July 29, 2013
    Date of Patent: October 11, 2022
    Assignee: BATTELLE MEMORIAL INSTITUTE
    Inventors: Brian A. Young, Angela T. Minard-Smith, Esley M. Heizer, Jr., Daniel M. Bornman, Mark E. Hester, Boyu Yang
  • Patent number: 10718016
    Abstract: Short Tandem Repeats are currently used by law enforcement and others, for example, for the identification of individuals by DNA matching. A method is described herein that uses WPD to classify and identify repeating sequences in nucleotide sequences from the position and frequency information contained within nucleotide sequences. This decomposition allows for the quick classification of nucleotide sequences (i.e., reads) into two different classes, including, for example, one class that contains sequencer reads that contain a repeat motif with non-repeat sequence on either flank, and another class that contains sequencer reads that do not contain any repeat sequence.
    Type: Grant
    Filed: June 16, 2017
    Date of Patent: July 21, 2020
    Assignee: BATTELLE MEMORIAL INSTITUTE
    Inventors: Joseph J. Regensburger, Aaron J. Sander, Jared M. Schuetter, Daniel M. Bornman, Seth A. Faith, Scott C. Nelson, Brian A. Young
  • Publication number: 20170292155
    Abstract: Short Tandem Repeats are currently used by law enforcement and others, for example, for the identification of individuals by DNA matching. A method is described herein that uses WPD to classify and identify repeating sequences in nucleotide sequences from the position and frequency information contained within nucleotide sequences. This decomposition allows for the quick classification of nucleotide sequences (i.e., reads) into two different classes, including, for example, one class that contains sequencer reads that contain a repeat motif with non-repeat sequence on either flank, and another class that contains sequencer reads that do not contain any repeat sequence.
    Type: Application
    Filed: June 16, 2017
    Publication date: October 12, 2017
    Inventors: Joseph J. Regensburger, Aaron J. Sander, Jared M. Schuetter, Daniel M. Bornman, Seth A. Faith, Scott C. Nelson, Brian A. Young
  • Patent number: 9708653
    Abstract: Short Tandem Repeats are currently used by law enforcement and others, for example, for the identification of individuals by DNA matching. A method is described herein that uses WPD to classify and identify repeating sequences in nucleotide sequences from the position and frequency information contained within nucleotide sequences. This decomposition allows for the quick classification of nucleotide sequences (i.e., reads) into two different classes, including, for example, one class that contains sequencer reads that contain a repeat motif with non-repeat sequence on either flank, and another class that contains sequencer reads that do not contain any repeat sequence.
    Type: Grant
    Filed: February 15, 2013
    Date of Patent: July 18, 2017
    Assignee: BATTELLE MEMORIAL INSTITUTE
    Inventors: Joseph J. Regensburger, Aaron J. Sander, Jared M. Schuetter, Daniel M. Bornman, Seth A. Faith, Scott C. Nelson, Brian A. Young
  • Publication number: 20150051083
    Abstract: Short Tandem Repeats are currently used by law enforcement and others, for example, for the identification of individuals by DNA matching. A method is described herein that uses WPD to classify and identify repeating sequences in nucleotide sequences from the position and frequency information contained within nucleotide sequences. This decomposition allows for the quick classification of nucleotide sequences (i.e., reads) into two different classes, including, for example, one class that contains sequencer reads that contain a repeat motif with non-repeat sequence on either flank, and another class that contains sequencer reads that do not contain any repeat sequence.
    Type: Application
    Filed: February 15, 2013
    Publication date: February 19, 2015
    Inventors: Joseph J. Regensburger, Aaron J. Sander, Jared M. Schuetter, Daniel M. Bornman, Seth A. Faith, Scott C. Nelson, Brian A. Young
  • Publication number: 20150032381
    Abstract: In one illustrative embodiment, an allelotyping method may include selecting a plurality of text strings that each represent a nucleotide sequence that was read by a massively parallel sequencing (MPS) instrument, where the nucleotide sequences represented by the selected plurality of text strings each correspond to a particular locus, comparing the selected plurality of text strings to one another to determine an abundance count for each unique text string included in the selected plurality of text strings, and determining one or more alleles for the particular locus by comparing the abundance count for each unique text string included in the selected plurality of text strings to an abundance threshold.
    Type: Application
    Filed: July 29, 2013
    Publication date: January 29, 2015
    Inventors: Brian A. Young, Angela T. Minard-Smith, Esley M. Heizer, JR., Daniel M. Bornman, Mark E. Hester, Boyu Yang
  • Publication number: 20150032385
    Abstract: In at least one illustrative embodiment, a method may comprise selecting a first plurality of text strings that each represent a nucleotide sequence that was read by a massively parallel sequencing instrument, where the nucleotide sequences represented by the selected first plurality of text strings each correspond to a first target locus, comparing the selected first plurality of text strings to one another to determine an abundance count for each unique text string included in the selected first plurality of text strings, identifying a first number of unique text strings included in the selected first plurality of text strings as representing noise responses, and determining a method detection limit as a function of the abundance counts for the first number of unique text strings identified as representing noise responses.
    Type: Application
    Filed: September 17, 2014
    Publication date: January 29, 2015
    Inventors: Brian A. Young, Esley M. Heizer, JR., Angela T. Minard-Smith, Nancy J. McMillan, Gokhan Yavas, Daniel M. Bornman