Αποτελέσματα αναζήτησης - 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 από Aaron Hinz, David E. Larson, Christopher Smith, Yves V. Brun
Έκδοση 2003Artigo -
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VarScan: variant detection in massively parallel sequencing of individual and pooled samples από Daniel C. Koboldt, Ken Chen, Todd Wylie, David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding
Έκδοση 2009Artigo -
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SomaticSniper: identification of somatic point mutations in whole genome sequencing data από 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
Έκδοση 2011Artigo -
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VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing από 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
Έκδοση 2012Artigo -
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CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data από 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
Έκδοση 2009Artigo -
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Bam-readcount - rapid generation of basepair-resolution sequence metrics από 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
Έκδοση 2022Pré-impressão -
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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation από 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
Έκδοση 2009Artigo -
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Mapping and characterization of structural variation in 17,795 human genomes από 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
Έκδοση 2020Artigo -
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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects από 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
Έκδοση 2018Artigo -
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Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers από 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
Έκδοση 2016Artigo -
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Background Mutations in Parental Cells Account for Most of the Genetic Heterogeneity of Induced Pluripotent Stem Cells από 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
Έκδοση 2012Artigo -
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Integrated analysis of germline and somatic variants in ovarian cancer από 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
Έκδοση 2014Artigo -
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The Alzheimer's Disease Sequencing Project: Study design and sample selection από 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
Έκδοση 2017Artigo
Εργαλεία αναζήτησης:
Σχετικά θέματα
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