Next Generation Clinical Diagnostics: The Sequence of Events

作者: Nicole Hoppman , David I. Smith , Eric W. Klee , Matthew J. Ferber

DOI: 10.1007/978-1-4614-8127-0_13

关键词:

摘要: The development of automated sequencing platforms based upon capillary electrophoresis and fluorescently labeled terminator bases made it possible to generate the first draft sequence human genome. However, what started as an effort develop new technologies entire genomes cheaper faster than electrophoresis-based has engendered a revolution that resulted in tremendous increases output capacity. Since introduction these so-called next-generation 2006, various been increasing greater fivefold every year. This led dramatic correspondingly decreased costs for DNA sequencing. These will quickly make whole genome so affordable inevitably become routine part clinical practice. In this chapter we review discuss potential applications transformative technology.

参考文章(67)
Tina Brooks, Law Library. Supreme Court of the United States. Petitions for Writ of Certiorari. University of Kentucky College of Law College of Law. ,(2012)
Katherine E. Cullen, Encyclopedia of life science ,(2009)
Giovanni Maglia, Andrew J. Heron, David Stoddart, Deanpen Japrung, Hagan Bayley, ANALYSIS OF SINGLE NUCLEIC ACID MOLECULES WITH PROTEIN NANOPORES Methods in Enzymology. ,vol. 475, pp. 591- 623 ,(2010) , 10.1016/S0076-6879(10)75022-9
John Aach, Joseph V. Thakuria, Jason Bobe, George M. Church, Jeantine E. Lunshof, Misha Angrist, Daniel B. Vorhaus, Margret R. Hoehe, Personal genomes in progress: from the Human Genome Project to the Personal Genome Project Dialogues in clinical neuroscience. ,vol. 12, pp. 47- 60 ,(2010)
Mary-Kayt N Jones, Richard Jh Smith, Nonsyndromic Hearing Loss and Deafness, DFNB1 University of Washington, Seattle. ,(2016)
Richard Williams, Sergio G Peisajovich, Oliver J Miller, Shlomo Magdassi, Dan S Tawfik, Andrew D Griffiths, Amplification of complex gene libraries by emulsion PCR Nature Methods. ,vol. 3, pp. 545- 550 ,(2006) , 10.1038/NMETH896
Thomas J Albert, Michael N Molla, Donna M Muzny, Lynne Nazareth, David Wheeler, Xingzhi Song, Todd A Richmond, Chris M Middle, Matthew J Rodesch, Charles J Packard, George M Weinstock, Richard A Gibbs, Direct selection of human genomic loci by microarray hybridization. Nature Methods. ,vol. 4, pp. 903- 905 ,(2007) , 10.1038/NMETH1111
Benjamin A Flusberg, Dale R Webster, Jessica H Lee, Kevin J Travers, Eric C Olivares, Tyson A Clark, Jonas Korlach, Stephen W Turner, Direct detection of DNA methylation during single-molecule, real-time sequencing Nature Methods. ,vol. 7, pp. 461- 465 ,(2010) , 10.1038/NMETH.1459
Jonathan M. Rothberg, Wolfgang Hinz, Todd M. Rearick, Jonathan Schultz, William Mileski, Mel Davey, John H. Leamon, Kim Johnson, Mark J. Milgrew, Matthew Edwards, Jeremy Hoon, Jan F. Simons, David Marran, Jason W. Myers, John F. Davidson, Annika Branting, John R. Nobile, Bernard P. Puc, David Light, Travis A. Clark, Martin Huber, Jeffrey T. Branciforte, Isaac B. Stoner, Simon E. Cawley, Michael Lyons, Yutao Fu, Nils Homer, Marina Sedova, Xin Miao, Brian Reed, Jeffrey Sabina, Erika Feierstein, Michelle Schorn, Mohammad Alanjary, Eileen Dimalanta, Devin Dressman, Rachel Kasinskas, Tanya Sokolsky, Jacqueline A. Fidanza, Eugeni Namsaraev, Kevin J. McKernan, Alan Williams, G. Thomas Roth, James Bustillo, An integrated semiconductor device enabling non-optical genome sequencing Nature. ,vol. 475, pp. 348- 352 ,(2011) , 10.1038/NATURE10242