@article{
 title = {Determining exon connectivity in complex mRNAs by nanopore sequencing},
 type = {article},
 year = {2015},
 identifiers = {[object Object]},
 pages = {204},
 volume = {16},
 websites = {http://genomebiology.com/2015/16/1/204},
 publisher = {Genome Biology},
 id = {a6284611-7aca-3c2e-b5c7-daeb5f360fac},
 created = {2017-09-18T09:15:15.620Z},
 file_attached = {true},
 profile_id = {1c95d708-d42d-399e-b365-9d34fead1a19},
 last_modified = {2017-09-18T09:21:28.278Z},
 read = {false},
 starred = {false},
 authored = {true},
 confirmed = {true},
 hidden = {false},
 citation_key = {Bolisetty2015},
 abstract = {Short-read high-throughput RNA sequencing, though powerful, is limited in its ability to directly measure exon connectivity in mRNAs that contain multiple alternative exons located farther apart than the maximum read length. Here, we use the Oxford Nanopore MinION sequencer to identify 7,899 'full-length' isoforms expressed from four Drosophila genes, Dscam1, MRP, Mhc, and Rdl. These results demonstrate that nanopore sequencing can be used to deconvolute individual isoforms and that it has the potential to be a powerful method for comprehensive transcriptome characterization.},
 bibtype = {article},
 author = {Bolisetty, Mohan T. and Rajadinakaran, Gopinath and Graveley, Brenton R.},
 journal = {Genome Biology},
 number = {1}
}

{"_id":"6d2zWTiMeBmyWhtAx","bibbaseid":"bolisetty-rajadinakaran-graveley-determiningexonconnectivityincomplexmrnasbynanoporesequencing-2015","downloads":0,"creationDate":"2017-09-18T08:46:38.747Z","title":"Determining exon connectivity in complex mRNAs by nanopore sequencing","author_short":["Bolisetty, M., T.","Rajadinakaran, G.","Graveley, B., R."],"year":2015,"bibtype":"article","biburl":null,"bibdata":{"title":"Determining exon connectivity in complex mRNAs by nanopore sequencing","type":"article","year":"2015","identifiers":"[object Object]","pages":"204","volume":"16","websites":"http://genomebiology.com/2015/16/1/204","publisher":"Genome Biology","id":"a6284611-7aca-3c2e-b5c7-daeb5f360fac","created":"2017-09-18T09:15:15.620Z","file_attached":"true","profile_id":"1c95d708-d42d-399e-b365-9d34fead1a19","last_modified":"2017-09-18T09:21:28.278Z","read":false,"starred":false,"authored":"true","confirmed":"true","hidden":false,"citation_key":"Bolisetty2015","abstract":"Short-read high-throughput RNA sequencing, though powerful, is limited in its ability to directly measure exon connectivity in mRNAs that contain multiple alternative exons located farther apart than the maximum read length. Here, we use the Oxford Nanopore MinION sequencer to identify 7,899 'full-length' isoforms expressed from four Drosophila genes, Dscam1, MRP, Mhc, and Rdl. These results demonstrate that nanopore sequencing can be used to deconvolute individual isoforms and that it has the potential to be a powerful method for comprehensive transcriptome characterization.","bibtype":"article","author":"Bolisetty, Mohan T. and Rajadinakaran, Gopinath and Graveley, Brenton R.","journal":"Genome Biology","number":"1","bibtex":"@article{\n title = {Determining exon connectivity in complex mRNAs by nanopore sequencing},\n type = {article},\n year = {2015},\n identifiers = {[object Object]},\n pages = {204},\n volume = {16},\n websites = {http://genomebiology.com/2015/16/1/204},\n publisher = {Genome Biology},\n id = {a6284611-7aca-3c2e-b5c7-daeb5f360fac},\n created = {2017-09-18T09:15:15.620Z},\n file_attached = {true},\n profile_id = {1c95d708-d42d-399e-b365-9d34fead1a19},\n last_modified = {2017-09-18T09:21:28.278Z},\n read = {false},\n starred = {false},\n authored = {true},\n confirmed = {true},\n hidden = {false},\n citation_key = {Bolisetty2015},\n abstract = {Short-read high-throughput RNA sequencing, though powerful, is limited in its ability to directly measure exon connectivity in mRNAs that contain multiple alternative exons located farther apart than the maximum read length. Here, we use the Oxford Nanopore MinION sequencer to identify 7,899 'full-length' isoforms expressed from four Drosophila genes, Dscam1, MRP, Mhc, and Rdl. These results demonstrate that nanopore sequencing can be used to deconvolute individual isoforms and that it has the potential to be a powerful method for comprehensive transcriptome characterization.},\n bibtype = {article},\n author = {Bolisetty, Mohan T. and Rajadinakaran, Gopinath and Graveley, Brenton R.},\n journal = {Genome Biology},\n number = {1}\n}","author_short":["Bolisetty, M., T.","Rajadinakaran, G.","Graveley, B., R."],"urls":{"Paper":"http://bibbase.org/service/mendeley/1c95d708-d42d-399e-b365-9d34fead1a19/file/4c50e3e3-afa5-990b-1d27-4b082a649826/2015-Determining_exon_connectivity_in_complex_mRNAs_by_nanopore_sequencing.pdf.pdf","Website":"http://genomebiology.com/2015/16/1/204"},"bibbaseid":"bolisetty-rajadinakaran-graveley-determiningexonconnectivityincomplexmrnasbynanoporesequencing-2015","role":"author","downloads":0},"search_terms":["determining","exon","connectivity","complex","mrnas","nanopore","sequencing","bolisetty","rajadinakaran","graveley"],"keywords":[],"authorIDs":[]}