Resultats de la cerca - David E. Larson
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The <i>Caulobacter crescentus</i> polar organelle development protein PodJ is differentially localized and is required for polar targeting of the PleC development regulator per Aaron Hinz, David E. Larson, Christopher Smith, Yves V. Brun
Publicat 2003Artigo -
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VarScan: variant detection in massively parallel sequencing of individual and pooled samples per Daniel C. Koboldt, Ken Chen, Todd Wylie, David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding
Publicat 2009Artigo -
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SomaticSniper: identification of somatic point mutations in whole genome sequencing data per David E. Larson, Christopher Harris, Ken Chen, Daniel C. Koboldt, Travis E. Abbott, David J. Dooling, Timothy J. Ley, Elaine R. Mardis, Richard K. Wilson, Li Ding
Publicat 2011Artigo -
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VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing per 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
Publicat 2012Artigo -
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CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data per 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
Publicat 2009Artigo -
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Bam-readcount - rapid generation of basepair-resolution sequence metrics per Ajay Khanna, David E. Larson, Sridhar Nonavinkere Srivatsan, Matthew Mosior, Travis Abbott, Susanna Kiwala, Timothy J. Ley, Eric J. Duncavage, Matthew J. Walter, Jason Walker, Obi L. Griffith, Malachi Griffith, Christopher A. Miller
Publicat 2022Pré-impressão -
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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation per 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
Publicat 2009Artigo -
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Mapping and characterization of structural variation in 17,795 human genomes per Haley Abel, David E. Larson, Allison Regier, Colby Chiang, Indraniel Das, Krishna Kanchi, Ryan M. Layer, Benjamin M. Neale, William Salerno, Catherine Reeves, Steven Buyske, Tara C. Matise, Donna M. Muzny, Michael C. Zody, Eric S. Lander, Susan K. Dutcher, Nathan O. Stitziel, Ira M. Hall
Publicat 2020Artigo -
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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects per Allison Regier, Yossi Farjoun, David E. Larson, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan, Bo-Juen Chen, Manisha Kher, Eric Banks, Darren C. Ames, Adam C. English, Heng Li, Jinchuan Xing, Yeting Zhang, Tara C. Matise, Gonçalo R. Abecasis, Will Salerno, Michael C. Zody, Benjamin M. Neale, Ira M. Hall
Publicat 2018Artigo -
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Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers per Christopher A. Miller, Yevgeniy Gindin, Charles Lu, Obi L. Griffith, Malachi Griffith, Dong Shen, Jeremy Hoog, Tiandao Li, David E. Larson, Mark A. Watson, Sherri R. Davies, Kelly K. Hunt, Vera J. Suman, Jacqueline Snider, Thomas Walsh, Graham A. Colditz, Katherine DeSchryver, Richard K. Wilson, Elaine R. Mardis, Matthew J. Ellis
Publicat 2016Artigo -
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Background Mutations in Parental Cells Account for Most of the Genetic Heterogeneity of Induced Pluripotent Stem Cells per Margaret A. Young, David E. Larson, Chiao-Wang Sun, Daniel R. George, Li Ding, Chris Miller, Ling Lin, Kevin M. Pawlik, Ken Chen, Xian Fan, Heather K. Schmidt, Joelle Kalicki-Veizer, Lisa L. Cook, Gary W. Swift, Ryan Demeter, Michael C. Wendl, Mark S. Sands, Elaine R. Mardis, Richard K. Wilson, Tim M. Townes, Timothy J. Ley
Publicat 2012Artigo -
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Integrated analysis of germline and somatic variants in ovarian cancer per Krishna Kanchi, Kimberly Johnson, Charles Lu, Michael D. McLellan, Mark D.M. Leiserson, Michael C. Wendl, Qunyuan Zhang, Daniel C. Koboldt, Mingchao Xie, Cyriac Kandoth, Joshua F. McMichael, Matthew A. Wyczalkowski, David E. Larson, Heather K. Schmidt, Christopher A. Miller, Robert S. Fulton, Paul T. Spellman, Elaine R. Mardis, Todd E. Druley, Timothy A. Graubert, Paul J. Goodfellow, Benjamin J. Raphael, Richard K. Wilson, Li Ding
Publicat 2014Artigo -
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The Alzheimer's Disease Sequencing Project: Study design and sample selection per Gary W. Beecham, Joshua C. Bis, Eden R. Martin, Seung Hoan Choi, Anita L. DeStefano, Cornelia M. van Duijn, Myriam Fornage, S.B. Gabriel, Daniel C. Koboldt, David E. Larson, A.C. Naj, Bruce M. Psaty, William Salerno, William S. Bush, Tatiana Foroud, Ellen M. Wijsman, Lindsay A. Farrer, Alison Goate, Jonathan L. Haines, Margaret A. Pericak‐Vance, Eric Boerwinkle, Richard Mayeux, Sudha Seshadri, Gerard D. Schellenberg
Publicat 2017Artigo
Eines de cerca:
Matèries relacionades
Biology
Genetics
Gene
Computational biology
Mutation
Cancer research
Genome
Medicine
Cancer
Computer science
Genotype
DNA sequencing
Exome
Exome sequencing
Single-nucleotide polymorphism
Internal medicine
Myeloid leukemia
Oncology
Germline mutation
Leukemia
Myeloid
Botany
Data mining
Human genome
Identification (biology)
Missense mutation
Phenotype
Somatic cell
Somatic evolution in cancer
Whole genome sequencing