http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9738930-B2

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filingDate 2012-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_607d30098ae929ad8659f16ffff28056
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publicationDate 2017-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9738930-B2
titleOfInvention Paired end bead amplification and high throughput sequencing
abstract The present invention is related to genomic nucleotide sequencing. In particular, the invention describes a paired end sequencing method that enables the sequencing of unique read pairs by co-localizing both 5′ ends on a single emulsion polymerase chain reaction bead. The method may use a customized forked adaptor primer pair that is compatible with massively parallel sequencing techniques. The compositions and methods disclosed herein contemplate sequencing complex genomes, amplified genomic regions, as well as detecting chromosomal structural rearrangements.
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priorityDate 2011-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID24794037
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ38087
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8E7Y1

Total number of triples: 310.