@article{
 title = {Nanopore sequencing: From imagination to reality},
 type = {article},
 year = {2015},
 identifiers = {[object Object]},
 pages = {25-31},
 volume = {61},
 id = {ab9fc928-68f1-39b9-89d4-c25ea6a5bd3f},
 created = {2017-09-18T09:15:19.429Z},
 file_attached = {true},
 profile_id = {1c95d708-d42d-399e-b365-9d34fead1a19},
 last_modified = {2017-09-18T09:17:07.342Z},
 read = {false},
 starred = {false},
 authored = {true},
 confirmed = {true},
 hidden = {false},
 citation_key = {Bayley2015},
 abstract = {DNA sequencing and hence genomics have been transformed over the last decade by the commercialization of inexpensive, massively parallel, short-read, sequencing technology. Nonetheless, a new generation of single-molecule DNA sequencers, which uses nanopore technology, is initiating a further upheaval in genomics. These instruments are portable, capable of reads of over 100 kb, cheap and fast. Nanopore sequencing, a huge technical challenge, took over 25 years to develop. Today's availability of a commercial nanopore sequencing device can be traced to the 1990s when nucleic acid translocation through nanopores was first observed, stochastic sensing developed and the high-resolution structure of a protein nanopore solved. The nanopore platform that has been developed is also capable of the single-molecule detection of a wide variety of additional analytes of medical interest, ranging from small molecules to post-translationally modified proteins.},
 bibtype = {article},
 author = {Bayley, Hagan},
 journal = {Clinical Chemistry},
 number = {1}
}

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