MutS based SNP detection, genome scanning and rare sequence enrichment

Information

  • Research Project
  • 7220122
  • ApplicationId
    7220122
  • Core Project Number
    R43GM080035
  • Full Project Number
    1R43GM080035-01
  • Serial Number
    80035
  • FOA Number
    PA-06-20
  • Sub Project Id
  • Project Start Date
    3/1/2007 - 17 years ago
  • Project End Date
    2/29/2008 - 16 years ago
  • Program Officer Name
    PORTNOY, MATTHEW
  • Budget Start Date
    3/1/2007 - 17 years ago
  • Budget End Date
    2/29/2008 - 16 years ago
  • Fiscal Year
    2007
  • Support Year
    1
  • Suffix
  • Award Notice Date
    2/15/2007 - 18 years ago
Organizations

MutS based SNP detection, genome scanning and rare sequence enrichment

[unreadable] DESCRIPTION (provided by applicant): MutS based SNP detection, genome scanning and rare sequence enrichment The goal of this project is to develop MutS based assays for SNP detection, rare sequence detection, rare sequence isolation and genome scanning for SNP discovery. The approach will be to use end-blocking of heteroduplexes, which has been shown to improve the stability of MutS binding. Initial experiments will involve SNP detection and rare SNP detection and isolation using synthetic oligonucleotides and will utilize Gene Check's Immobilized Mismatch Binding Protein method of SNP detection. These experiments will also determine if end- blocking improves MutS binding to mismatches that are poorly bound in vivo and in vitro without end-blocking. Three different end-blocks will be tested (four-way DNA junctions, streptavidin/biotin complexes and antibody/biotin complexes)and MutS will be obtained from three different bacteria (E. coli, T. aquaticus and T. thermophilis). Successful conditions will be applied to PCR amplicons for SNP and rare SNP detection by amplifying genomic DNA of known genotypes mixed in various ratios. Finally, bacterial genomic DNA will be used in experiments testing end-blocking in applications for genomic scanning for unknown SNPs and for direct genotyping of known SNPs without amplification. MutS based SNP detection, genome scanning and rare sequence enrichment Development of a MutS based method of SNP detection and discovery and rare SNP and sequence detection and isolation will help meet an increasing need for SNP discovery and whole genome scanning in the move toward personalized medicine. The ability to detect rare SNPs and sequences will have immediate clinical impact, both for humans in such areas as diagnostic scanning for rare mutations among normal cells as in tumor margins, and in veterinary diagnostics by allowing rapid and inexpensive analysis of pooled samples for infectious agents and genetic diseases or production traits. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    100000
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:100000\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    GENE CHECK, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    Greeley
  • Organization State
    CO
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    80634
  • Organization District
    UNITED STATES