Resultados da pesquisa

454 sequencing put to the test using the complex genome of barley Por Thomas Wicker, Edith Schlagenhauf, Andreas Graner, Timothy J. Close, Beat Keller, Nils Stein

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Prenatal Whole Genome Sequencing Por Greer Donley, Sara Chandros Hull, Benjamin E. Berkman

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Underlying Data for Sequencing the Mitochondrial Genome with the Massively Parallel Sequencing Platform Ion Torrent™ PGM™ Por Seung Bum Seo, Xiangpei Zeng, Jonathan L. King, Bobby LaRue, Mourad Assidi, Mohamed H. Alqahtani, Antti Sajantila, Bruce Budowle

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Prospects for Personalized Cardiovascular Medicine Por Geoffrey S. Ginsburg, Mark Donahue, L. Kristin Newby

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FOXM1 binds directly to non-consensus sequences in the human genome Por Deborah A. Sanders, Michael V. Gormally, Giovanni Marsico, Dario Beraldi, David Tannahill, Shankar Balasubramanian

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High-Throughput Sequencing Technologies Por Jason Reuter, Damek V. Spacek, M Snyder

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Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data Por Qi Liu, Yan Guo, Jiang Li, Jirong Long, Bing Zhang, Yu Shyr

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Clinical application of next-generation sequencing for Mendelian diseases Por Saumya Shekhar Jamuar, Ene‐Choo Tan

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Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age Por Kimberly A. Kaphingst, Jennifer Ivanovich, Barbara B. Biesecker, Rebecca Dresser, Jiae Seo, L. G. Dressler, Paul J. Goodfellow, Melody S. Goodman

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Personal genomes in progress: from the Human Genome Project to the Personal Genome Project Por Jeantine E. Lunshof, Jason Bobe, John Aach, Misha Angrist, Joseph V. Thakuria, Daniel B. Vorhaus, Margret R. Hoehe, George M. Church

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The sheep genome reference sequence: a work in progress Por Alan Archibald, N. E. Cockett, Brian P. Dalrymple, T. Faraut, James Kijas, J F Maddox, John C. McEwan, V. Hutton Oddy, H. W. Raadsma, Claire M. Wade, Jian Wang, W. Wang, Xun Xu

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Cpipe: a shared variant detection pipeline designed for diagnostic settings Por Simon Sadedin, Harriet Dashnow, Paul A. James, Melanie Bahlo, Denis C. Bauer, Andrew Lonie, Sebastian Lunke, Ivan Macciocca, Jason P. Ross, Kirby Siemering, Zornitza Stark, Susan M. White, Graham R. Taylor, Clara Gaff, Alicia Oshlack, Natalie Thorne

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Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes Por Tony S. Shen, Stefan Hans Pajaro-Van de Stadt, Nai Chien Yeat, Jimmy Lin

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Kiwi genome provides insights into evolution of a nocturnal lifestyle Por Diana Le Duc, Gabriel Renaud, Arunkumar Krishnan, Markus Sällman Almén, Leon Huynen, Sonja J. Prohaska, Matthias Ongyerth, Bárbara Domingues Bitarello, Helgi B. Schiöth, Michael Hofreiter, Peter F. Stadler, Kay Prüfer, David M. Lambert, Janet Kelso, Torsten Schöneberg

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Defining “mutation” and “polymorphism” in the era of personal genomics Por Roshan Karki, Deep Pandya, Robert C. Elston, Cristiano Ferlini

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It's more than stamp collecting: how genome sequencing can unify biological research Por Stephen Richards

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The Future of Personal Genomics Por Amy L. McGuire, Mildred K. Cho, Sean E. McGuire, Timothy Caulfield

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16^th IHIW : Review of HLA typing by NGS Por Dianne De Santis, David Dinauer, Jamie L. Duke, M Kellis, Cherie L. Holcomb, Curt Lind, Kate Mackiewicz, Dimitri Monos, Arnav Moudgil, Paul J. Norman, Peter Parham, Ariella Sasson, Richard Allcock

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Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project Por Saskia C. Sanderson, Michael D. Linderman, Sabrina A. Suckiel, George A. Díaz, Randi E. Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E. Schadt

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Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories Por Jennifer Saam, Christopher Arnell, Aaron Theisen, Kelsey Moyes, Ingrid Marino, Kirstin M. Roundy, Richard Wenstrup

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