http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007118144-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_859b59c620b5fe20451b18f238b2347d
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1fb733ba1516ec5c0e8a279e811a128f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6841
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-34
filingDate 2007-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f89c94c97bb6bf1786faea19d98e55b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a424406a14c1b390f67c54950aca941
publicationDate 2007-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2007118144-A2
titleOfInvention High resolution chromosomal mapping
abstract The present invention generally relates to spatial and structural genomic analysis compositions, which can be used for the mapping of chromosomes and structural analyses of chromosomal rearrangements, including the entire chromosome, as well as specific portions or regions of interest of the chromosomes. In some embodiments, multiple portions of the genome can be distinguished, for instance, using a first detection entity (13) and a second detection entity (14) different from the first detection entity. The detection entities may be immobilized relative to oligonucleotides (11, 12), which may be selected to bind to different locations within the chromosome (25). For instance, the oligonucleotides may be at least substantially complementary to the chromosome, e.g., substantially complementary to a specific location of the chromosome.
priorityDate 2006-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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