http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2007907-A2
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9cb16f3933087407282046d3265c0c4e |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6837 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6874 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2007-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_228aa16988b675f72e102202d56326fb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a628d9416a9fda78db487a94362d9fcc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54f98f1c1934f46da72f5769ddc09539 |
publicationDate | 2008-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-2007907-A2 |
titleOfInvention | Reagents, methods, and libraries for gel-free bead-based sequencing |
abstract | The present invention provides methods for determining a nucleic acid sequence by performing successive cycles of duplex extension along a single stranded template. The cycles comprise steps of extension, ligation, and, preferably, cleavage. In certain embodiments the methods make use of extension probes containing phosphorothiolate linkages and employ agents appropriate to cleave such linkages. In certain embodiments the methods make use of extension probes containing an abasic residue or a damaged base and employ agents appropriate to cleave linkages between a nucleoside and an abasic residue and/or agents appropriate to remove a damaged base from a nucleic acid. The invention provides methods of determining information about a sequence using at least two distinguishably labeled probe families. In certain embodiments the methods acquire less than 2 bits of information from each of a plurality of nucleotides in the template in each cycle. In certain embodiments the sequencing reactions are performed on templates attached to microparticles, which are immobilized in or on a semi-solid support or attached to a substrate. The invention further provides sets of labeled extension probes containing phosphorothiolate linkages or trigger residues that are suitable for use in the method. In addition, the invention includes performing multiple sequencing reactions on a single template by removing initializing oligonucleotides and extended strands and performing subsequent reactions using different initializing oligonucleotides. The invention further provides efficient methods for preparing templates, particularly for performing sequencing multiple different templates in parallel. The invention also provides methods for performing ligation and cleavage. The invention also provides new libraries of nucleic acid fragments containing paired tags, and methods of preparing microparticles having multiple different templates (e.g., containing paired tags) attached thereto and of sequencing the templates individually. The invention also provides automated sequencing systems, flow cells, image processing methods, and computer-readable media that store computer-executable instructions (e.g., to perform the image-processing methods) and/or sequence information. In certain embodiments the sequence information is stored in a database. The invention further provides blocking oligonucleotides and methods of use thereof to facilitate sequencing. Further provided are arrays comprising microparticles having templates attached thereto and attached to a substrate in the absence of a semi-solid medium and methods of sequencing the templates. The invention also provides arrays of nucleic acid colonies produced using microparticles to 'imprint' templates on a semi-solid medium or substrate, and methods of sequencing thereof. |
priorityDate | 2006-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 493.