Methods for genetic analysis of DNA to detect sequence...

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S091200, C536S024330

Reexamination Certificate

active

07659054

ABSTRACT:
The presently claimed invention concerns a method for biasing the amplification of the DNA molecules in a sample such that a nucleic acid molecule having a specific nucleotide at a selected position (e.g., a polymorphic site) is preferentially amplified relative to an otherwise identical nucleic acid molecule not having the specific nucleotide at the selected position. The method entails amplification of target nucleic acid molecules using a pair of primers one of which causes the incorporation into the amplification product of a sequence that interferes with amplification of nucleic acid molecules not having the specific nucleotide at the selected position. The method is useful for preferentially amplifying at least a portion of one allele of a gene relative to another, different allele of the gene in a sample containing both alleles of the gene.

REFERENCES:
patent: 5595890 (1997-01-01), Newton et al.
patent: 5612179 (1997-03-01), Simons
patent: 5639611 (1997-06-01), Wallace et al.
patent: 5789568 (1998-08-01), Simons
patent: 5804383 (1998-09-01), Gruenert et al.
patent: 5851762 (1998-12-01), Simons
patent: 5853989 (1998-12-01), Jeffreys et al.
patent: 5972614 (1999-10-01), Ruano et al.
patent: 6277607 (2001-08-01), Tyagi et al.
patent: 6326145 (2001-12-01), Whitcombe et al.
patent: 6361940 (2002-03-01), Van Ness et al.
patent: WO 00/31300 (2000-06-01), None
Bolla MK et al. High-throughput method for determination of apolipoprotein E genotypes with use of restriction digestion analysis by microplate array diagonal gel electrophoresis. Clin Chem., 41(11): 1599-1604, 1995.
Caetano-Anolles G et al. Generation of sequence signatures from DNA amplification fingerprints with mini-hairpin and microsatellite primers. Biotechniques, 20: 1044-1056, 1996.
Clark, A.G., et al. “Haplotype Stucture and Population Genetic Inferences from . . . ”,American Journal of Human Genetics63: 595-612, 1998.
Hubert et al., “Sperm Typing Allows Accurate Measurement Of The Recombination Fraction Between D3S2 And D3S3 On The Short Arm Of Human Chromosome 3”,Genomics. Apr. 1992;12(4):683-687).
Lo, Y.M. et al., “Direct haplotype determination by double ARMS: specificity, sensitivity and genetic applications”,Nucleic Acids ResearchJuly 11:19 (13):3561-7, 1991).
Newton et al., “Amplification Refractory Mutation System For Prenatal Diagnosis And Carrier Assessment In Cystic Fibrosis”,Lancet. Dec 23-30; 2 (8678-8679):1481-3, 1989.
Newton et al., “Analysis Of Any Point Mutation In DNA. The Amplification Refractory Mutation System (ARMS)”,Nucleic Acids Res.vol. 17, 2503-2516, 1989).
Nickerson, D. A., et al., “DNA sequence diversity in a 9.7-kb . . . ”,Nature Genetics19: 233-240, 1998.
Ruano et al., “Haplotype Of Multiple Polymorphisms Resolved By Enzymatic Amplification Of Single DNA Molecules”,Proc Natl Acad Sci U S A1990 87(16):6296-6300.
Terwilliger et al., “Linkage disequilibrium mapping of complex disease: fantasy or reality?”,Current Opinion in Biotechnology9: 578-594, 1998.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Methods for genetic analysis of DNA to detect sequence... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Methods for genetic analysis of DNA to detect sequence..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Methods for genetic analysis of DNA to detect sequence... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-4160867

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.