Suchergebnisse - Michael D. McLellan

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  1. 1
    PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data

    PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data von Ken Chen, Michael D. McLellan, Li Ding, Michael C. Wendl, Yumi Kasai, Richard K. Wilson, Elaine R. Mardis

    Veröffentlicht 2007
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  2. 2
    MSIsensor: microsatellite instability detection using paired tumor-normal sequence data

    MSIsensor: microsatellite instability detection using paired tumor-normal sequence data von Beifang Niu, Kai Ye, Qunyuan Zhang, Charles Lu, Mingchao Xie, Michael D. McLellan, Michael C. Wendl, Li Ding

    Veröffentlicht 2013
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  3. 3
    Clonal evolution revealed by whole genome sequencing in a case of primary myelofibrosis transformed to secondary acute myeloid leukemia

    Clonal evolution revealed by whole genome sequencing in a case of primary myelofibrosis transformed to secondary acute myeloid leukemia von Elizabeth K. Engle, D. Fisher, Chris Miller, Michael D. McLellan, Robert S. Fulton, David M. Moore, Richard K. Wilson, T J Ley, Stephen T. Oh

    Veröffentlicht 2014
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  4. 4
    VarScan: variant detection in massively parallel sequencing of individual and pooled samples

    VarScan: variant detection in massively parallel sequencing of individual and pooled samples von Daniel C. Koboldt, Ken Chen, Todd Wylie, David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding

    Veröffentlicht 2009
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  5. 5
    Reduced<i>PU.1</i>expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARα

    Reduced<i>PU.1</i>expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARα von Matthew J. Walter, John S. Park, Rhonda E. Ries, Steven K. Lau, Michael D. McLellan, Sara R. Jaeger, Richard K. Wilson, Elaine R. Mardis, Timothy J. Ley

    Veröffentlicht 2005
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  6. 6
    VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing

    VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing von Daniel C. Koboldt, Qunyuan Zhang, David E. Larson, Dong Shen, Michael D. McLellan, Ling Lin, Christopher A. Miller, Elaine R. Mardis, Li Ding, Richard K. Wilson

    Veröffentlicht 2012
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  7. 7
    CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data

    CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data von Qunyuan Zhang, Li Ding, David E. Larson, Daniel C. Koboldt, Michael D. McLellan, Ken Chen, Xiaoqi Shi, Aldi T. Kraja, Elaine R. Mardis, Richard K. Wilson, Ingrid B. Borecki, Michael A. Province

    Veröffentlicht 2009
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  8. 8
    Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif

    Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif von Mark P. Hamilton, Kimal Rajapakshe, Sean M. Hartig, Boris Reva, Michael D. McLellan, Cyriac Kandoth, Jun Li, Travis Zack, Preethi H. Gunaratne, David A. Wheeler, Cristian Coarfa, Sean E. McGuire

    Veröffentlicht 2013
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  9. 9
    Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma

    Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma von David H. Gutmann, Michael D. McLellan, Ibrahim Hussain, John W. Wallis, Lucinda Fulton, Robert S. Fulton, Vincent Magrini, Ryan Demeter, Todd Wylie, Cyriac Kandoth, Jeffrey R. Leonard, Abhijit Guha, Christopher A. Miller, Jun Li, Elaine R. Mardis

    Veröffentlicht 2012
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  10. 10
    Novel <i>MEK1</i> Mutation Identified by Mutational Analysis of Epidermal Growth Factor Receptor Signaling Pathway Genes in Lung Adenocarcinoma

    Novel <i>MEK1</i> Mutation Identified by Mutational Analysis of Epidermal Growth Factor Receptor Signaling Pathway Genes in Lung Adenocarcinoma von Jenifer L. Marks, Yixuan Gong, Dhananjay Chitale, Ben Golas, Michael D. McLellan, Yumi Kasai, Li Ding, Elaine R. Mardis, Richard K. Wilson, David B. Solit, Ross L. Levine, Kathrin Michel, Roman K. Thomas, Valerie W. Rusch, Marc Ladanyi, William Pao

    Veröffentlicht 2008
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  11. 11
    BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

    BreakDancer: an algorithm for high-resolution mapping of genomic structural variation von Ken Chen, John W. Wallis, Michael D. McLellan, David E. Larson, Joelle Kalicki, Craig Pohl, Sean McGrath, Michael C. Wendl, Qunyuan Zhang, Devin P. Locke, Xiaoqi Shi, Robert S. Fulton, Timothy J. Ley, Richard K. Wilson, Li Ding, Elaine R. Mardis

    Veröffentlicht 2009
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  12. 12
    Recurrent DNMT3A mutations in patients with myelodysplastic syndromes

    Recurrent DNMT3A mutations in patients with myelodysplastic syndromes von Matthew J. Walter, Li Ding, Dong Shen, Jieya Shao, Marcus Grillot, Michael D. McLellan, Robert S. Fulton, H Schmidt, Joelle Kalicki-Veizer, Michele O’Laughlin, Cyriac Kandoth, Jack Baty, Peter Westervelt, John F. DiPersio, Elaine R. Mardis, Richard K. Wilson, T J Ley, Timothy A. Graubert

    Veröffentlicht 2011
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  13. 13
    Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4

    Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4 von Jenifer L. Marks, Michael D. McLellan, Maureen F. Zakowski, Alex E. Lash, Yumi Kasai, Stephen Broderick, Inderpal S. Sarkaria, DuyKhanh Pham, Bhuvanesh Singh, Tracie L. Miner, Ginger Fewell, Lucinda Fulton, Elaine R. Mardis, Richard K. Wilson, Mark G. Kris, Valerie W. Rusch, Harold Varmus, William Pao

    Veröffentlicht 2007
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  14. 14
    Protein-structure-guided discovery of functional mutations across 19 cancer types

    Protein-structure-guided discovery of functional mutations across 19 cancer types von Beifang Niu, Adam Scott, Sohini Sengupta, Matthew H. Bailey, Prag Batra, Jie Ning, Matthew A. Wyczalkowski, Wen-Wei Liang, Qunyuan Zhang, Michael D. McLellan, Sam Q. Sun, Piyush Tripathi, Carolyn Lou, Kai Ye, R. Jay Mashl, John Wallis, Michael C. Wendl, Feng Chen, Li Ding

    Veröffentlicht 2016
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  15. 15
    Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes

    Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes von Mark D.M. Leiserson, Fabio Vandin, Hsin-Ta Wu, Jason R. Dobson, Jonathan V Eldridge, Jacob Thomas, Alexandra Papoutsaki, Younhun Kim, Beifang Niu, Michael D. McLellan, Michael S. Lawrence, Abel González-Pérez, David Tamborero, Yu‐Wei Cheng, Gregory Ryslik, Núria López-Bigas, Gad Getz, Li Ding, Benjamin J. Raphael

    Veröffentlicht 2014
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  16. 16
    Optimized polyepitope neoantigen DNA vaccines elicit neoantigen-specific immune responses in preclinical models and in clinical translation

    Optimized polyepitope neoantigen DNA vaccines elicit neoantigen-specific immune responses in preclinical models and in clinical translation von Lijin Li, Xiuli Zhang, Xiaoli Wang, Samuel W. Kim, John M. Herndon, Michelle Becker‐Hapak, Beatriz M. Carreno, Nancy B. Myers, Mark Sturmoski, Michael D. McLellan, Christopher A. Miller, Tanner M. Johanns, Benjamin Tan, Gavin P. Dunn, Timothy P. Fleming, Ted H. Hansen, S. Peter Goedegebuure, William E. Gillanders

    Veröffentlicht 2021
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  17. 17
    Mutational landscape and significance across 12 major cancer types

    Mutational landscape and significance across 12 major cancer types von Cyriac Kandoth, Michael D. McLellan, Fabio Vandin, Kai Ye, Beifang Niu, Charles Lu, Mingchao Xie, Qunyuan Zhang, Joshua F. McMichael, Matthew A. Wyczalkowski, Mark D.M. Leiserson, Christopher A. Miller, John S. Welch, Matthew J. Walter, Michael C. Wendl, Timothy J. Ley, Richard K. Wilson, Benjamin J. Raphael, Li Ding

    Veröffentlicht 2013
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  18. 18
    Systematic discovery of complex insertions and deletions in human cancers

    Systematic discovery of complex insertions and deletions in human cancers von Kai Ye, Jiayin Wang, Reyka G. Jayasinghe, Eric-Wubbo Lameijer, Joshua F. McMichael, Jie Ning, Michael D. McLellan, Mingchao Xie, Song Cao, Venkata Yellapantula, Kuan‐lin Huang, Adam Scott, Steven M. Foltz, Beifang Niu, Kimberly J. Johnson, Matthijs Moed, P. Eline Slagboom, Feng Chen, Michael C. Wendl, Li Ding

    Veröffentlicht 2015
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  19. 19
    Age-related mutations associated with clonal hematopoietic expansion and malignancies

    Age-related mutations associated with clonal hematopoietic expansion and malignancies von Mingchao Xie, Charles Lu, Jiayin Wang, Michael D. McLellan, Kimberly Johnson, Michael C. Wendl, Joshua F. McMichael, Heather K. Schmidt, Venkata Yellapantula, Christopher A. Miller, Bradley A. Ozenberger, John S. Welch, Daniel C. Link, Matthew J. Walter, Elaine R. Mardis, John F. DiPersio, Feng Chen, Richard K. Wilson, Timothy J. Ley, Li Ding

    Veröffentlicht 2014
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  20. 20
    Clonal diversity of recurrently mutated genes in myelodysplastic syndromes

    Clonal diversity of recurrently mutated genes in myelodysplastic syndromes von Matthew J. Walter, Dong Shen, Jin Shao, Li Ding, Brian S. White, Cyriac Kandoth, Christopher A. Miller, Bing Niu, Michael D. McLellan, Nathan D. Dees, Robert S. Fulton, Kerryn Elliot, Simon Heath, Marcus Grillot, Peter Westervelt, Daniel C. Link, John F. DiPersio, Elaine R. Mardis, Timothy J. Ley, Richard K. Wilson, Timothy A. Graubert

    Veröffentlicht 2013
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