Existing and Emerging Technologies for Tumor Genomic Profiling

作者: Laura E. MacConaill

DOI: 10.1200/JCO.2012.46.5948

关键词:

摘要: Ongoing global genome characterization efforts are revolutionizing our knowledge of cancer genomics and tumor biology. In parallel, information gleaned from these studies on driver gene alterations—mutations, copy number alterations, translocations, and/or chromosomal rearrangements—can be leveraged, in principle, to develop a cohesive framework for individualized treatment. These possibilities have been enabled, large degree, by revolutionary advances genomic technologies that facilitate systematic profiling hallmark genetic alterations at increasingly fine resolutions. innovations existing technologies, as well the many emerging will likely continue advance translational precision medicine.

参考文章(109)
Iris Schrijver, Nazneen Aziz, Daniel H. Farkas, Manohar Furtado, Andrea Ferreira Gonzalez, Timothy C. Greiner, Wayne W. Grody, Tina Hambuch, Lisa Kalman, Jeffrey A. Kant, Roger D. Klein, Debra G.B. Leonard, Ira M. Lubin, Rong Mao, Narasimhan Nagan, Victoria M. Pratt, Mark E. Sobel, Karl V. Voelkerding, Jane S. Gibson, Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology. The Journal of Molecular Diagnostics. ,vol. 14, pp. 525- 540 ,(2012) , 10.1016/J.JMOLDX.2012.04.006
Robert J. Lonigro, Catherine S. Grasso, Dan R. Robinson, Xiaojun Jing, Yi-Mi Wu, Xuhong Cao, Michael J. Quist, Scott A. Tomlins, Kenneth J. Pienta, Arul M. Chinnaiyan, Detection of somatic copy number alterations in cancer using targeted exome capture sequencing. Neoplasia. ,vol. 13, pp. 1019- 1025 ,(2011) , 10.1593/NEO.111252
Andrea Warrick, Erin M. Forbes, Dylan Nelson, Emily Justusson, Judith Levine, Tanaya L. Neff, Janice Patterson, Ajia Presnell, Arin McKinley, Laura J. Winter, Christie Dewey, Amy Harlow, Oscar Barney, Brian J. Druker, Kathryn G. Schuff, Christopher L. Corless, Carol Beadling, Michael C. Heinrich, Multiplex Mutation Screening by Mass Spectrometry: Evaluation of 820 Cases from a Personalized Cancer Medicine Registry The Journal of Molecular Diagnostics. ,vol. 13, pp. 504- 513 ,(2011) , 10.1016/J.JMOLDX.2011.04.003
Matthew Meyerson, Stacey Gabriel, Gad Getz, Advances in understanding cancer genomes through second-generation sequencing Nature Reviews Genetics. ,vol. 11, pp. 685- 696 ,(2010) , 10.1038/NRG2841
A Kallioniemi, O. Kallioniemi, D Sudar, D Rutovitz, J. Gray, F Waldman, D Pinkel, Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors Science. ,vol. 258, pp. 818- 821 ,(1992) , 10.1126/SCIENCE.1359641
Lloyd M. Smith, Jane Z. Sanders, Robert J. Kaiser, Peter Hughes, Chris Dodd, Charles R. Connell, Cheryl Heiner, Stephen B. H. Kent, Leroy E. Hood, Fluorescence detection in automated DNA sequence analysis Nature. ,vol. 321, pp. 674- 679 ,(1986) , 10.1038/321674A0
Jeffery A Schloss, How to get genomes at one ten-thousandth the cost. Nature Biotechnology. ,vol. 26, pp. 1113- 1115 ,(2008) , 10.1038/NBT1008-1113
Laura E. MacConaill, Levi A. Garraway, Clinical Implications of the Cancer Genome Journal of Clinical Oncology. ,vol. 28, pp. 5219- 5228 ,(2010) , 10.1200/JCO.2009.27.4944