Accurate sequencing by hybridization for DNA diagnostics and individual genomics (original) (raw)

References

  1. Ko, L.J. and Prives, C. 1996. p53, puzzle and paradigm. Genes Dev. 10: 1054–1072.
    Article CAS Google Scholar
  2. Wall, J., Cai, S., and Chebab, F.F. 1995. A 31-mutation assay for cystic fibrosis testing in the clinical molecular diagnostic laboratory. Hum. Mutat. 5: 333–338.
    Article CAS Google Scholar
  3. Durocher, F., Sharruck-Eidens, D., McClure, M., Labrie, F., Skolnick, M.H.,, Goldgar, D.E., and Simard, J. 1996. Comparison of BRCA1 polymorphisms, rare sequence variants and/or misense mutations in unaffected and breast/ovarian cancer populations. Hum. Mol. Genet. 6: 835–842.
    Article Google Scholar
  4. Studencki, A.B. and Wallace, R.B. 1984. Allele-specific hybridization using oligonucleotide probe of very high specific activity: discrimination of human beta A- and S-globin genes. DNA 3: 7–15.
    Article CAS Google Scholar
  5. Okayama, H., Curiel, D.T., Brantly, M.L., Holmes, M.D., and Crystal, R.G. 1984. Rapid, nonradioactive detection of mutations in the human by allele-specific amplification. J. Lab. Clin. Med. 114: 105–113.
    Google Scholar
  6. Tavtigian, S.V., Oliphant, A., and Shattuck-Eidens, D. In press. Genomic organization, functional analysis and mutation screening of BRCA1 and BRCA2. Accomplishments in Cancer Research 1996. Fortner, J.G. and Sharp, P.A. (eds.) General Motors Cancer Research Foundation, Dallas, TX.
  7. Drmanac, R. and Crkvenjakov, R. 1987. Method of sequencing of genomes by hybridization with oligonucleotide probes. Yugoslav patent application 570/87.
  8. Drmanac, R. and Crkvenjakov, R. 1993. Method of sequencing of genomes by hybridization with oligonucleotide probes. US patent 5,202,231.
  9. Drmanac, R., Labat, I., Brukner, I., and Crkvenjakov, R. 1989. Sequencing of megabase plus DNA by hybridization: Theory of the method. Genomics 4: 114–127.
    Article CAS Google Scholar
  10. Drmanac, R., Drmanac, S., Strezoska, Z., Paunesku, T., Labat, I., Zaremski, M., et al. 1993. DNA sequence determination by hybridization: A strategy for efficient large-scale sequencing. Science 260: 1649–1652.
    Article CAS Google Scholar
  11. Chee, M., Yang, R., Hubbell, E., Berno, A., Huang, X.C., Stern, D., et al. 1996. Accessing genetic information with high-density DNA arrays. Science 274: 610–613.
    Article CAS Google Scholar
  12. Hacia, J.G., Brody, L., Chee, M.S., Fodor, S.P.A. and Colins, S. 1996. Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two color florescence analysis. Nat. Genet. 14: 441–449.
    Article CAS Google Scholar
  13. Sugimoto, N., Nakano, S., Yoreyama, M. and Haneda, K. 1996. Improved ther-modynamic parameters and helix initiation factor to predict stability of DNA duplexes. Nucl. Acids Res. 24: 4501–4505.
    Article CAS Google Scholar
  14. Thomas, T.C., Schmidt, C., and Neer, E.J. 1993. G-protein alpha-o-subunit: mutation of conserved cysteins identifies a sutaunit contact surface and alters GDP affinity. Proc. Natl. Acad. Sci. USA 90: 10295–10299.
    Article CAS Google Scholar
  15. Drmanac, R., Strezoska, Z., Labat, I., Drmanac, S. and Crkvenjakov, R. 1990. Reliable hybridization of oligonucleotides as short as six nucleotides. DNA Cell Biol. 9: 527–534.
    Article CAS Google Scholar

Download references