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  1. 1
    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™ af Seung Bum Seo, Xiangpei Zeng, Jonathan L. King, Bobby LaRue, Mourad Assidi, Mohamed H. Alqahtani, Antti Sajantila, Bruce Budowle

    Udgivet 2015
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  2. 2
    Detection of Genomic Structural Variants from Next-Generation Sequencing Data

    Detection of Genomic Structural Variants from Next-Generation Sequencing Data af Lorenzo Tattini, Romina D’Aurizio, Alberto Magi

    Udgivet 2015
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  3. 3
    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 af Tony S. Shen, Stefan Hans Pajaro-Van de Stadt, Nai Chien Yeat, Jimmy Lin

    Udgivet 2015
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  4. 4
    Functional Genomics in the Mouse: Phenotype-Based Mutagenesis Screens

    Functional Genomics in the Mouse: Phenotype-Based Mutagenesis Screens af John C. Schimenti, Maja Bućan

    Udgivet 1998
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  5. 5
    Advances in computational approaches for prioritizing driver mutations and significantly mutated genes in cancer genomes

    Advances in computational approaches for prioritizing driver mutations and significantly mutated genes in cancer genomes af Feixiong Cheng, Junfei Zhao, Zhongming Zhao

    Udgivet 2015
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  6. 6
    Translating cancer genomes and transcriptomes for precision oncology

    Translating cancer genomes and transcriptomes for precision oncology af Sameek Roychowdhury, Arul M. Chinnaiyan

    Udgivet 2015
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  7. 7
    Next-generation sequencing

    Next-generation sequencing af Jorge S. Reis‐Filho

    Udgivet 2009
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  8. 8
    Expanding the computational toolbox for mining cancer genomes

    Expanding the computational toolbox for mining cancer genomes af Li Ding, Michael C. Wendl, Joshua F. McMichael, Benjamin J. Raphael

    Udgivet 2014
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  9. 9
    Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches

    Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches af Haley Abel, Eric J. Duncavage

    Udgivet 2013
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  10. 10
    Understanding genomic alterations in cancer genomes using an integrative network approach

    Understanding genomic alterations in cancer genomes using an integrative network approach af Edwin Wang

    Udgivet 2012
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  11. 11
    Novel Molecular and Computational Methods Improve the Accuracy of Insertion Site Analysis in Sleeping Beauty-Induced Tumors

    Novel Molecular and Computational Methods Improve the Accuracy of Insertion Site Analysis in Sleeping Beauty-Induced Tumors af Benjamin T. Brett, Katherine E. Berquam‐Vrieze, Kishore Nannapaneni, Jian Huang, Todd E. Scheetz, Adam J. Dupuy

    Udgivet 2011
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  12. 12
    A physical map of the human genome

    A physical map of the human genome af John D. McPherson, Marco A. Marra, LaDeana Hillier, R Waterston, Asif Chinwalla, John Wallis, Mandeep Sekhon, Kristine M. Wylie, Elaine R. Mardis, Richard K. Wilson, Robert S. Fulton, Tamara A. Kucaba, Caryn Wagner-McPherson, W. Brad Barbazuk, Simon G. Gregory, Sean Humphray, Lisa French, Richard S. Evans, Graeme Bethel, Adam Whittaker, Jane L. Holden, Owen T McCann, Andrew Dunham, Carol Soderlund, Clare L. Scott, David Bentley, Gregory D. Schuler, Hsiu-Chuan Chen, Wonhee Jang, Eric D. Green, Jacquelyn R. Idol, Valerie V. Maduro, Kate Montgomery, Eunice Lee, Ashley Miller, Suzanne Emerling, Raju Kucherlapati, Richard A. Gibbs, Stephen W. Scherer, James H. Gorrell, Erica Sodergren, Kerstin P. Clerc-Blankenburg, Paul E. Tabor, Susan L. Naylor, Dawn Garcia, Pieter J. de Jong, Joseph J. Catanese, Norma J. Nowak, Kazutoyo Osoegawa, Shizhen Qin, Lee Rowen, Anuradha Madan, Monica Dors, Leroy Hood, Barbara J. Trask, Cynthia Friedman, Hillary F. Massa, Vivian G. Cheung, Ilan R. Kirsch, Thomas Reid, Raluca Yonescu, Jean Weissenbach, Thomas Brüls, Roland Heilig, Elbert Branscomb, Anne S. Olsen, Norman A. Doggett, Jan‐Fang Cheng, Trevor Hawkins, R Myers, Jin Shang, Lucı́a Ramı́rez, Jeremy Schmutz, Olivia Velasquez, Kami Dixon, Nancy Stone, David R. Cox, David Haussler, W. James Kent, Terrence S. Furey, Sanja Rogić, Scot Kennedy, Steven J.M. Jones, André Rosenthal, Gaiping Wen, Markus B. Schilhabel, Gernot Glöeckner, Gerald Nyakatura, Reiner Siebert, Brigitte Schlegelberger, Julie R. Korenberg, Xiao–Ning Chen, Asao Fujiyama, Masahira Hattori, Atsushi Toyoda, Tetsushi Yada, Hong‐Seok Park, Yoshiyuki Sakaki, Nobuyoshi Shimizu, Shuichi Asakawa

    Udgivet 2001
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  13. 13
    Cancer whole-genome sequencing: present and future

    Cancer whole-genome sequencing: present and future af Hidewaki Nakagawa, Christopher P. Wardell, Mayuko Furuta, Hiroaki Taniguchi, Akihiro Fujimoto

    Udgivet 2015
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  14. 14
    Genomic and Functional Characteristics of Human Cytomegalovirus Revealed by Next-Generation Sequencing

    Genomic and Functional Characteristics of Human Cytomegalovirus Revealed by Next-Generation Sequencing af Steven Sijmons, Marc Van Ranst, Piet Maes

    Udgivet 2014
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  15. 15
    An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data

    An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data af Yuichi Shiraishi, Yusuke Sato, Kenichi Chiba, Yusuke Okuno, Yasunobu Nagata, Kenichi Yoshida, Norio Shiba, Yasuhide Hayashi, Haruki Kume, Yukio Homma, Masashi Sanada, Seishi Ogawa, Satoru Miyano

    Udgivet 2013
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  16. 16
    Quantitative phenotyping via deep barcode sequencing

    Quantitative phenotyping via deep barcode sequencing af Andrew Smith, Lawrence E. Heisler, Joseph Mellor, Fiona Kaper, Michael J. Thompson, Mark S. Chee, Frederick P. Roth, Guri Giaever, Corey Nislow

    Udgivet 2009
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  17. 17
    Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads

    Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads af Yu Bai, Min Ni, Blerta Cooper, Yi Wei, Wen Fury

    Udgivet 2014
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  18. 18
    Genome-wide analysis of noncoding regulatory mutations in cancer

    Genome-wide analysis of noncoding regulatory mutations in cancer af Nils Weinhold, Anders J. Skanderup, Nikolaus Schultz, Chris Sander, William Lee

    Udgivet 2014
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  19. 19
    DrGaP: A Powerful Tool for Identifying Driver Genes and Pathways in Cancer Sequencing Studies

    DrGaP: A Powerful Tool for Identifying Driver Genes and Pathways in Cancer Sequencing Studies af Xing Hua, Haiming Xu, Yaning Yang, Jun Zhu, Pengyuan Liu, Yan Lü

    Udgivet 2013
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  20. 20
    Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

    Screening the human exome: a comparison of whole genome and whole transcriptome sequencing af Elizabeth T. Cirulli, Abanish Singh, Kevin V. Shianna, Dongliang Ge, Jason P. Smith, Jessica M. Maia, Erin L. Heinzen, James J. Goedert, David B. Goldstein

    Udgivet 2010
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