Patents by Inventor Philip B. FEINBERG

Philip B. FEINBERG 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).

  • METHOD AND MARKERS FOR IDENTIFICATION AND RELATIVE QUANTIFICATION OF NUCLEIC ACID SEQUENCE, MUTATION, COPY NUMBER, OR METHYLATION CHANGES USING COMBINATIONS OF NUCLEASE, LIGATION, DEAMINATION, DNA REPAIR, AND POLYMERASE REACTIONS WITH CARRYOVER PREVENTION
    Publication number: 20230287484
    Abstract: The present invention relates to methods for identifying and/or quantifying low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, alternative non-coding sequences, alternative splicings, exon insertions, exon deletions, intron insertions, or other rearrangement at the genome level and/or methylated or hydroxymethylated nucleotide bases, as well as markers to identify early cancer, monitor cancer treatment, and identify early cancer recurrence.
    Type: Application
    Filed: April 29, 2021
    Publication date: September 14, 2023
    Inventors: Francis BARANY, Manny D. BACOLOD, Jianmin HUANG, Philip B. FEINBERG, Aashiq H. MIRZA, Sarah F. GIARDINA
  • Method for identification and quantification of nucleic acid expression, splice variant, translocation, copy number, or methylation changes
    Patent number: 11466311
    Abstract: The present invention relates to methods and devices for identifying and quantifying, including low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, alternative non-coding sequences, alternative splicings, exon insertions, exon deletions, intron insertions, or other rearrangement at the genome level and/or methylated nucleotide bases.
    Type: Grant
    Filed: June 6, 2019
    Date of Patent: October 11, 2022
    Assignee: CORNELL UNIVERSITY
    Inventors: Francis Barany, John William Efcavitch, Cristian Ruiz Rueda, Jianmin Huang, Philip B. Feinberg
  • MARKERS FOR IDENTIFYING AND QUANTIFYING OF NUCLEIC ACID SEQUENCE MUTATION, EXPRESSION, SPLICE VARIANT, TRANSLOCATION, COPY NUMBER, OR METHYLATION CHANGES
    Publication number: 20220243263
    Abstract: The present invention relates to methods for identifying and/or quantifying low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, alternative non-coding sequences, alternative splicings, exon insertions, exon deletions, intron insertions, or other rearrangement at the genome level and/or methylated nucleotide bases.
    Type: Application
    Filed: May 1, 2020
    Publication date: August 4, 2022
    Inventors: Francis BARANY, Manny D. BACOLOD, Jianmin HUANG, Aashiq H. MIRZA, Philip B. FEINBERG, Sarah F. GIARDINA
  • METHOD FOR IDENTIFICATION AND QUANTIFICATION OF NUCLEIC ACID EXPRESSION, SPLICE VARIANT, TRANSLOCATION, COPY NUMBER, OR METHYLATION CHANGES
    Publication number: 20190316187
    Abstract: The present invention relates to methods and devices for identifying and quantifying, including low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, alternative non-coding sequences, alternative splicings, exon insertions, exon deletions, intron insertions, or other rearrangement at the genome level and/or methylated nucleotide bases.
    Type: Application
    Filed: June 6, 2019
    Publication date: October 17, 2019
    Inventors: Francis Barany, John William Efcavitch, Cristian Ruiz Rueda, Jianmin Huang, Philip B. Feinberg
  • Method for identification and quantification of nucleic acid expression, splice variant, translocation, copy number, or methylation changes
    Patent number: 10344321
    Abstract: The present invention relates to methods and devices for identifying and quantifying, including low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, alternative non-coding sequences, alternative splicings, exon insertions, exon deletions, intron insertions, or other rearrangement at the genome level and/or methylated nucleotide bases.
    Type: Grant
    Filed: October 8, 2015
    Date of Patent: July 9, 2019
    Assignee: Cornell University
    Inventors: Francis Barany, John William Efcavitch, Cristian Ruiz Rueda, Jianmin Huang, Philip B. Feinberg
  • METHOD FOR IDENTIFICATION AND QUANTIFICATION OF NUCLEIC ACID EXPRESSION, SPLICE VARIANT, TRANSLOCATION, COPY NUMBER, OR METHYLATION CHANGES
    Publication number: 20180265917
    Abstract: The present invention relates to methods and devices for identifying and quantifying, including low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, alternative non-coding sequences, alternative splicings, exon insertions, exon deletions, intron insertions, or other rearrangement at the genome level and/or methylated nucleotide bases.
    Type: Application
    Filed: October 8, 2015
    Publication date: September 20, 2018
    Inventors: Francis BARANY, John William EFCAVITCH, Cristian RUIZ RUEDA, Jianmin HUANG, Philip B. FEINBERG