Patents by Inventor Marvin Moore

Marvin Moore 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).

  • VARIANT ANNOTATION, ANALYSIS AND SELECTION TOOL
    Publication number: 20230326547
    Abstract: Disclosed are methods for detecting and/or prioritizing phenotype-causing genomic variants and related software tools. The methods include genomic feature based analysis and can combine variant frequency information with sequence characteristics such as amino acid substation. The methods disclosed are useful in any genomics study; for example, rare and common disease gene discovery, tumor growth mutation detection, personalized medicine, agricultural analysis, and centennial analysis.
    Type: Application
    Filed: November 4, 2022
    Publication date: October 12, 2023
    Inventors: Mark YANDELL, Martin REESE, Chad HUFF, Hao HU, Marvin MOORE
  • VARIANT ANNOTATION, ANALYSIS AND SELECTION TOOL
    Publication number: 20200227135
    Abstract: Disclosed are methods for detecting and/or prioritizing phenotype-causing genomic variants and related software tools. The methods include genomic feature based analysis and can combine variant frequency information with sequence characteristics such as amino acid substation. The methods disclosed are useful in any genomics study; for example, rare and common disease gene discovery, tumor growth mutation detection, personalized medicine, agricultural analysis, and centennial analysis.
    Type: Application
    Filed: October 8, 2019
    Publication date: July 16, 2020
    Inventors: Mark YANDELL, Martin REESE, Chad HUFF, Hao HU, Marvin MOORE
  • VARIANT ANNOTATION, ANALYSIS AND SELECTION TOOL
    Publication number: 20130332081
    Abstract: Disclosed are methods for detecting and/or prioritizing phenotype-causing genomic variants and related software tools. The methods include genomic feature based analysis and can combine variant frequency information with sequence characteristics such as amino acid substation. The methods disclosed are useful in any genomics study; for example, rare and common disease gene discovery, tumor growth mutation detection, personalized medicine, agricultural analysis, and centennial analysis.
    Type: Application
    Filed: September 9, 2011
    Publication date: December 12, 2013
    Applicant: OMICIA INC
    Inventors: Martin G. Reese, Mark Yandell, Chad Huff, Hao Hu, Marvin Moore