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Emergence of single-molecule sequencing and potential for molecular diagnostic applications

Pages 659-666 | Published online: 09 Jan 2014

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Colin M Court, Jacob S Ankeny, Shuang Hou, Hsian-Rong Tseng & James S Tomlinson. (2015) Improving pancreatic cancer diagnosis using circulating tumor cells: prospects for staging and single-cell analysis. Expert Review of Molecular Diagnostics 15:11, pages 1491-1504.
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Yan Gao, Liwei Deng, Qin Yan, Yongqian Gao, Zengding Wu, Jinsen Cai, Daorui Ji, Gailing Li, Ping Wu, Huan Jin, Luyang Zhao, Song Liu, Liangjin Ge, Michael W. Deem & Jiankui He. (2016) Single molecule targeted sequencing for cancer gene mutation detection. Scientific Reports 6:1.
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Fernanda Veronese Oliveira, Carla Vecchione Gurgel, Tatiana Yuriko Kobayashi, Thiago José Dionísio, Lucimara Teixeira Neves, Carlos Ferreira Santos, Maria Aparecida Andrade Moreira Machado & Thais Marchini Oliveira. (2014) Amelogenesis Imperfecta and Screening of Mutation in Amelogenin Gene. Case Reports in Dentistry 2014, pages 1-5.
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Karel Knez, Dragana Spasic, Kris P. F. Janssen & Jeroen Lammertyn. (2014) Emerging technologies for hybridization based single nucleotide polymorphism detection. The Analyst 139:2, pages 353-370.
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Jiekun Xuan, Ying Yu, Tao Qing, Lei Guo & Leming Shi. (2013) Next-generation sequencing in the clinic: Promises and challenges. Cancer Letters 340:2, pages 284-295.
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C. Alexander Valencia, M. Ali Pervaiz, Ammar Husami, Yaping Qian & Kejian ZhangC. Alexander Valencia, M. Ali Pervaiz, Ammar Husami, Yaping Qian & Kejian Zhang. 2013. Next Generation Sequencing Technologies in Medical Genetics. Next Generation Sequencing Technologies in Medical Genetics 45 55 .
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Jessica M E van den Oever, Sahila Balkassmi, E Joanne Verweij, Maarten van Iterson, Phebe N Adama van Scheltema, Dick Oepkes, Jan M M van Lith, Mariëtte J V Hoffer, Johan T den Dunnen, Egbert Bakker & Elles M J Boon. (2012) Single Molecule Sequencing of Free DNA from Maternal Plasma for Noninvasive Trisomy 21 Detection. Clinical Chemistry 58:4, pages 699-706.
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John F. Thompson, Jeffrey G. Reifenberger, Eldar Giladi, Kristen Kerouac, Jaime Gill, Erik Hansen, Avak Kahvejian, Philipp Kapranov, Travis Knope, Doron Lipson, Kathleen E. Steinmann & Patrice M. Milos. (2012) Single-step capture and sequencing of natural DNA for detection of BRCA1 mutations . Genome Research 22:2, pages 340-345.
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Cristi R. King & Sharon Marsh. 2012. Principles of Pharmacogenetics and Pharmacogenomics. Principles of Pharmacogenetics and Pharmacogenomics 12 20 .
Paul Williams, Lakshmana Pendyala & Robert Superko. (2011) Survival bias and drug interaction can attenuate cross-sectional case-control comparisons of genes with health outcomes. An example of the kinesin-like protein 6 (KIF6) Trp719Arg polymorphism and coronary heart disease. BMC Medical Genetics 12:1.
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John F Thompson & Patrice M Milos. (2011) The properties and applications of single-molecule DNA sequencing. Genome Biology 12:2.
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Seokheun Choi, Michael Goryll, Lai Yi Mandy Sin, Pak Kin Wong & Junseok Chae. (2010) Microfluidic-based biosensors toward point-of-care detection of nucleic acids and proteins. Microfluidics and Nanofluidics 10:2, pages 231-247.
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Karl V. Voelkerding, Shale Dames & Jacob D. Durtschi. (2010) Next Generation Sequencing for Clinical Diagnostics-Principles and Application to Targeted Resequencing for Hypertrophic Cardiomyopathy. The Journal of Molecular Diagnostics 12:5, pages 539-551.
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Yi Fu & Joseph R. Lakowicz. (2010) Enhanced Single-Molecule Detection using Porous Silver Membrane. The Journal of Physical Chemistry C 114:16, pages 7492-7495.
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Alon Singer & Amit Meller. (2010) Nanopore‐based Sensing of Individual Nucleic Acid Complexes. Israel Journal of Chemistry 49:3-4, pages 323-331.
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