Genetic Models of Ocular Disease and Biostatistics

Information

  • Research Project
  • 10250836
  • ApplicationId
    10250836
  • Core Project Number
    P30EY010572
  • Full Project Number
    5P30EY010572-27
  • Serial Number
    010572
  • FOA Number
    PAR-17-322
  • Sub Project Id
    5453
  • Project Start Date
    5/1/1997 - 27 years ago
  • Project End Date
    8/31/2025 - a year from now
  • Program Officer Name
  • Budget Start Date
    9/1/2021 - 2 years ago
  • Budget End Date
    8/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    27
  • Suffix
  • Award Notice Date
    9/9/2021 - 2 years ago

Genetic Models of Ocular Disease and Biostatistics

PROJECT SUMMARY - GENETIC MODELS OF OCULAR DISEASE & BIOSTATISTICS The Genetic Models of Ocular Disease & Biostatistics module (formerly Molecular Genetics and Biostatistics) has been a mainstay providing essential support to NEI-funded PIs at the Casey Eye Institute. The overall goal of this module is to provide support for answering fundamental questions about the genetic mechanisms behind ocular disease. In the past, this core has provided two services: (1) DNA isolation from blood samples, saliva and tissue. Having a dedicated facility for the isolation of DNA ensures maximal DNA yield from patient material and reduces exposure to hazardous biological materials; 2) support for biostatistical analyses, which allows NEI investigators access to the most advanced statistical techniques ensuring that the appropriate methods are used both in the study design phase as well as for data analysis. Projects include analysis of complex gene expression arrays and RNA-seq datasets, large proteomics studies using TMT tags, optical coherence tomography (OCT) and OCT angiography (OCTA), bioinformatics and clinical research studies. While maintaining these two critical services, the Genetic Models of Ocular Disease & Biostatistics core has been expanded to offer two additional resources: (3) genotyping of cell, tissue and biological samples from a variety of species (including human, non- human primates, rat, mouse and pig). Genotyping using the QuantStudio real-time PCR machine and TaqMan chemistry is more cost-effective than traditional Sanger DNA sequencing; and (4) Establishing primary cell cultures from ocular tissues, as well as fibroblasts from patients with ocular disease. In the age of precision medicine, it is important to offer core services that reflect individual variability in genes and identifying gene variants associated with various ocular diseases. Moreover, offering both cell culture and genotyping services allows functional genotype-phenotype studies to be performed. Combined, these four services will enable our researchers to streamline their efforts to identify new molecular pathways involved in disease and should catalyze innovative avenues of ocular research to rapidly translate novel ideas from bench to patient bedside. Continuation of the Genetic Models of Ocular Disease & Biostatistics core will be instrumental in assisting new, as well as established, investigators at OHSU in obtaining NEI funding in the next 5 years.

IC Name
NATIONAL EYE INSTITUTE
  • Activity
    P30
  • Administering IC
    EY
  • Application Type
    5
  • Direct Cost Amount
    116491
  • Indirect Cost Amount
    62905
  • Total Cost
  • Sub Project Total Cost
    179396
  • ARRA Funded
    False
  • CFDA Code
  • Ed Inst. Type
  • Funding ICs
    NEI:179396\
  • Funding Mechanism
    RESEARCH CENTERS
  • Study Section
    ZEY1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    OREGON HEALTH & SCIENCE UNIVERSITY
  • Organization Department
  • Organization DUNS
    096997515
  • Organization City
    PORTLAND
  • Organization State
    OR
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    972393098
  • Organization District
    UNITED STATES