Patents by Inventor Katrin Heider

Katrin Heider 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: 20220025937
    Abstract: A sliding sleeve (1) of a vehicle transmission synchronization, wherein the tooth flanks (10) of the toothing (2) of the sliding sleeve (1) are surface-treated for enhanced friction.
    Type: Application
    Filed: December 17, 2019
    Publication date: January 27, 2022
    Applicant: Schaeffler Technologies AG & Co. KG
    Inventors: Katrin Heider, Knut Erdmann, Christoph Karl
  • Publication number: 20220017891
    Abstract: The present invention provides a method for detecting variant cell-free DNA (cfDNA) in a sample obtained from a subject, where analysis of the sample includes a size-selection step which separates out different fragment sizes of DNA. The sample may be a limited volume sample such as a blood, serum or plasma sample of less than 500 ?l (e.g. a blood or plasma sample of about 50 ?l), or other sample that has a low content of cfDNA. The sample may have been stored and/or dried and not have been processed to remove cells or cellular material prior to storage. The size-selection step may comprise filtering-out, depleting or removing genomic DNA (gDNA) fragments of >200 bp, >300 bp, >500 bp, >700 bp, >1000 bp, >1200 bp, >1500 bp, or >2000 bp prior to analysis, e.g. prior to DNA sequencing. The method may further comprise performing an analysis that summarises or combines data across multiple loci.
    Type: Application
    Filed: November 22, 2019
    Publication date: January 20, 2022
    Inventors: Katrin Heider, Jonathan Wan, Nitzan Rosenfeld
  • Publication number: 20200402613
    Abstract: The present invention provides a computer-implemented method for detecting cell-free DNA (cfDNA), such as circulating tumour DNA, in a DNA-containing sample obtained from a patient, the method comprising: (a) providing loci of interest comprising at least 2 mutation-containing loci representative of a tumour of the patient (“patient-specific loci”); (b) providing sequence data comprising sequence reads of a plurality of polynucleotide fragments from a DNA-containing sample from the patient, wherein said sequence reads span said at least 2 mutation-containing loci of step (a); (c) optionally, performing reads collapsing to group the sequence reads into read families; (d) calculating the mutant allele fraction across some or all of said at least 2 patient-specific loci, optionally wherein the mutant allele fraction is calculated by aggregating mutant reads and total reads; (e) classifying the sample as containing or not containing the target cfDNA based on the calculated mutant allele fraction.
    Type: Application
    Filed: March 6, 2019
    Publication date: December 24, 2020
    Inventors: Eyal Fisher, Katrin Heider, Charles Massie, Florent Mouliere, Nitzan Rosenfeld, Christopher G. Smith, Jonathan C.M. Wan