Exon Boundary Tags (EBTs) for Human Functional Genome Annotation

Information

  • Research Project
  • 7218834
  • ApplicationId
    7218834
  • Core Project Number
    R43HG004180
  • Full Project Number
    1R43HG004180-01
  • Serial Number
    4180
  • FOA Number
    PA-06-20
  • Sub Project Id
  • Project Start Date
    9/26/2006 - 19 years ago
  • Project End Date
    3/31/2007 - 18 years ago
  • Program Officer Name
    FEINGOLD, ELISE A
  • Budget Start Date
    9/26/2006 - 19 years ago
  • Budget End Date
    3/31/2007 - 18 years ago
  • Fiscal Year
    2006
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/25/2006 - 19 years ago

Exon Boundary Tags (EBTs) for Human Functional Genome Annotation

[unreadable] DESCRIPTION (provided by applicant): Project Summary/Abstract: The Human Genome Project has brought the field of functional genomics to the forefront of biological and pharmaceutical research. However, deciphering the function(s) of each gene in a high throughput format is complicated by alternative splicing and post-translational modifications of proteins. Serial Analysis of Vector Integration (SAVI(r)) is a patented method for high-throughput acquisition of genome-wide functional exons and gene expression profiling by sequencing only a certain length of each exon boundary as Exon Boundary Tag (EBT) after retroviral gene trapping. Since the EBTs generated will be proportioned to the copy numbers of corresponding mRNA molecules or alternative transcripts, quantification of acquired EBTs can reflect the transcription level for gene expression profiles between different treatments or cell types, such as cancer vs. normal cells, for pharmaceutical developments. Preliminary studies demonstrate the feasibility of generating unique data in this research field with a high potential for functional genome annotation, cDNA collection and exon/splice-specific microarray design. Project Narrative: The study we are proposing here is a high-throughput acquisition of genome-wide functional exons by sequencing only a certain length of each exon boundary to assemble open reading frames for functional genome annotation and gene expression profiling. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
  • Activity
    R43
  • Administering IC
    HG
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    98414
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    172
  • Ed Inst. Type
  • Funding ICs
    NHGRI:98414\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    NEWLINK GENETICS CORPORATION
  • Organization Department
  • Organization DUNS
    010664329
  • Organization City
    AMES
  • Organization State
    IA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    50010
  • Organization District
    UNITED STATES