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filingDate 1999-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_430a0e1ea24f01537ebef1f0e7ef1003
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bdc359db153dd2b8eb902fe570ac0862
publicationDate 1999-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9961665-A2
titleOfInvention Solution hybridization of nucleic acids with antisense probes having modified backbones
abstract The invention provides a method for rapidly, economically and efficiently sequencing and assaying nucleotides in a fluid medium using laser induced fluorescence of antisense probes. The probes can have anionic backbones of reduced negative charge. Suitable probes can include methylphosphonate backbones. When the hybridization complexes and unhybridized probes are separated prior to detection, the fluorescent intensity of the fluid test medium is inversely proportional to the number of mismatches between the probe and target. When the hybridization complexes and unhybridized probes are not separated prior to detection, the fluorescent intensity of the fluid test medium is inversely proportional to the hybridization efficiency of the probes with respect to the target sequence and proportional to the number of mismatches between the probe and target. The method can be used to identify accessible regions in folded nucleotide sequences, to determine the number of mismatched pairs in a hybridization complex, and to map genomes.
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