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  1. 1
    454 sequencing put to the test using the complex genome of barley

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

    出版 2006
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  2. 2
    Prenatal Whole Genome Sequencing

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

    出版 2012
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  3. 3
    Underlying Data for Sequencing the Mitochondrial Genome with the Massively Parallel Sequencing Platform Ion Torrent™ PGM™

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

    出版 2015
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  4. 4
    Prospects for Personalized Cardiovascular Medicine

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

    出版 2005
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  5. 5
    FOXM1 binds directly to non-consensus sequences in the human genome

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

    出版 2015
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  6. 6
    High-Throughput Sequencing Technologies

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

    出版 2015
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  7. 7
    Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data

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

    出版 2012
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  8. 8
    Clinical application of next-generation sequencing for Mendelian diseases

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

    出版 2015
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  9. 9
    Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age

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

    出版 2015
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  10. 10
    Personal genomes in progress: from the Human Genome Project to the Personal Genome Project

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

    出版 2010
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  11. 11
    The sheep genome reference sequence: a work in progress

    The sheep genome reference sequence: a work in progress 由 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

    出版 2010
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  12. 12
    Cpipe: a shared variant detection pipeline designed for diagnostic settings

    Cpipe: a shared variant detection pipeline designed for diagnostic settings 由 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

    出版 2015
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  13. 13
    Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes

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

    出版 2015
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  14. 14
    Kiwi genome provides insights into evolution of a nocturnal lifestyle

    Kiwi genome provides insights into evolution of a nocturnal lifestyle 由 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

    出版 2015
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  15. 15
    Defining “mutation” and “polymorphism” in the era of personal genomics

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

    出版 2015
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  16. 16
    It's more than stamp collecting: how genome sequencing can unify biological research

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

    出版 2015
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  17. 17
    The Future of Personal Genomics

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

    出版 2007
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  18. 18
    16<sup>th</sup> IHIW : Review of HLA typing by NGS

    16<sup>th</sup> IHIW : Review of HLA typing by NGS 由 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

    出版 2013
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  19. 19
    Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project

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

    出版 2015
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  20. 20
    Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories

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

    出版 2015
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