Patents by Inventor Subramaniam Srinivasan

Subramaniam Srinivasan 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).

  • SYSTEM AND METHODS FOR DETECTING GENETIC VARIATION
    Publication number: 20220254443
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant. In some aspects, systems and methods of detecting genetic variation are provided.
    Type: Application
    Filed: January 24, 2022
    Publication date: August 11, 2022
    Applicant: MYRIAD WOMEN'S HEALTH, INC.
    Inventors: Hunter Richards, Eric Evans, Balaji Srinivasan, Subramaniam Srinivasan, Abhik Shah, A. Scott Patterson, Clement Chu
  • System and methods for detecting genetic variation
    Patent number: 9092401
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant. In some aspects, systems and methods of detecting genetic variation are provided.
    Type: Grant
    Filed: October 31, 2012
    Date of Patent: July 28, 2015
    Assignee: Counsyl, Inc.
    Inventors: Hunter Richards, Eric Evans, Balaji Srinivasan, Subramaniam Srinivasan, Abhik Shah, A. Scott Patterson, Clement Chu
  • System and Methods for Detecting Genetic Variation
    Publication number: 20150205914
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant. In some aspects, systems and methods of detecting genetic variation are provided.
    Type: Application
    Filed: October 10, 2014
    Publication date: July 23, 2015
    Inventors: Hunter RICHARDS, Eric EVANS, Balaji SRINIVASAN, Subramaniam SRINIVASAN, Abhik SHAH, A. Scott PATTERSON, Clement CHU
  • METHODS AND COMPOSITIONS FOR ENRICHMENT OF TARGET POLYNUCLEOTIDES
    Publication number: 20140162278
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant.
    Type: Application
    Filed: December 10, 2013
    Publication date: June 12, 2014
    Applicant: Counsyl, Inc.
    Inventors: Hunter Richards, Eric Evans, Balaji Srinivasan, Subramaniam Srinivasan, Clement Chu
  • System and Methods for Detecting Genetic Variation
    Publication number: 20140121116
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant. In some aspects, systems and methods of detecting genetic variation are provided.
    Type: Application
    Filed: October 31, 2012
    Publication date: May 1, 2014
    Applicant: Counsyl, Inc.
    Inventors: Hunter Richards, Eric EVANS, Balaji SRINIVASAN, Subramaniam SRINIVASAN, Abhik SHAH, A. Scott Patterson, Clement CHU
  • METHODS AND COMPOSITIONS FOR HIGH-THROUGHPUT SEQUENCING
    Publication number: 20140024541
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant.
    Type: Application
    Filed: July 17, 2012
    Publication date: January 23, 2014
    Applicant: Counsyl, Inc.
    Inventors: Hunter Richards, Eric Evans, Balaji Srinivasan, Subramaniam Srinivasan, Clement Chu
  • APPARATUS AND METHODS FOR HIGH-THROUGHPUT SEQUENCING
    Publication number: 20140024536
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant.
    Type: Application
    Filed: July 17, 2012
    Publication date: January 23, 2014
    Applicant: Counsyl, Inc.
    Inventors: Hunter Richards, Eric Evans, Balaji Srinivasan, Subramaniam Srinivasan, Clement Chu
  • METHODS AND COMPOSITIONS FOR ENRICHMENT OF TARGET POLYNUCLEOTIDES
    Publication number: 20140024542
    Abstract: The invention provides methods, apparatuses, and compositions for high-throughput amplification sequencing of specific target sequences in one or more samples. In some aspects, barcode-tagged polynucleotides are sequenced simultaneously and sample sources are identified on the basis of barcode sequences. In some aspects, sequencing data are used to determine one or more genotypes at one or more loci comprising a causal genetic variant.
    Type: Application
    Filed: July 17, 2012
    Publication date: January 23, 2014
    Applicant: Counsyl, Inc.
    Inventors: Hunter Richards, Eric Evans, Balaji Srinivasan, Subramaniam Srinivasan, Clement Chu