http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002534098-A
Outgoing Links
Predicate | Object |
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classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10T436-143333 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6837 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6841 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6855 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6874 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N37-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6874 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6855 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6837 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6827 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6841 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-566 |
filingDate | 2000-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2002-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2002534098-A |
titleOfInvention | Accelerated Identification of Single Nucleotide Polymorphisms and Alignment of Clones in Genome Sequencing |
abstract | (57) [Summary]nThe present invention is directed to a method for assembling a map of an organism's DNA or portions thereof. A DNA library of organisms is provided, wherein segments or sequences of the human genome are found in one or more clones of the library. A representation of the genome is made, and nucleic acid sequencing methods are derived from the representation. This sequence information is analyzed to detect duplication of clones from the representation. Duplicate and sequence information of clones from separate representations is combined to assemble a genome map of the organism. Once a genomic map is obtained, genomic sequence information from multiple individuals can be applied to the map and compared to each other to identify single nucleotide polymorphisms. These single nucleotide polymorphisms are detected by (1) extensive PCR amplification to produce a genomic representation, and (2) hybridization of the ligation product to a support to induce a ligation detection reaction step that is captured. Possible and alleles are quantified. |
priorityDate | 1999-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 194.