http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004209299-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-1093
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6855
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
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filingDate 2004-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aab8f5095bea6be7e82ac2b20cfdc155
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89b5c7599546528f0a839deb56aa1b45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6ae743c9345963df2f16aa25189d279
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f5afae565b1222f44d22be564c5c4df
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73f3be9acc123427d1080f35f05137a2
publicationDate 2004-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004209299-A1
titleOfInvention In vitro DNA immortalization and whole genome amplification using libraries generated from randomly fragmented DNA
abstract The present invention regards a variety of methods and compositions for whole genome amplification. In a particular aspect of the present invention, there is a method of amplifying a genome in a non-biased manner utilizing adaptor-attached randomly generated fragments following modification of the DNA ends prior to the adaptor attachment. In an additional aspect of the present invention, there are methods and compositions for whole genome amplification regarding a one-step endonuclease cleavage and linker ligation reaction.
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1791
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID31772786
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP11936
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Total number of triples: 723.