Որոնման արդյունքները - David E. Larson
- Ցուցադրվում են 1 - 20 արդյունքները 45
- Գնացեք Հաջորդ էջ
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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 Aaron Hinz, David E. Larson, Christopher Smith, Yves V. Brun
Հրապարակվել է 2003Artigo -
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CTNS Mutations in an American-Based Population of Cystinosis Patients Vorasuk Shotelersuk, David E. Larson, Yair Anikster, Geraldine A. McDowell, Rosemary Lemons, Isa Bernardini, Juanru Guo, Jess G. Thoene, William A. Gahl
Հրապարակվել է 1998Artigo -
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VarScan: variant detection in massively parallel sequencing of individual and pooled samples Daniel C. Koboldt, Ken Chen, Todd Wylie, David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding
Հրապարակվել է 2009Artigo -
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SomaticSniper: identification of somatic point mutations in whole genome sequencing data 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
Հրապարակվել է 2011Artigo -
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VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing 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
Հրապարակվել է 2012Artigo -
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CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data 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
Հրապարակվել է 2009Artigo -
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Bam-readcount - rapid generation of basepair-resolution sequence metrics 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
Հրապարակվել է 2022Pré-impressão -
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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation 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
Հրապարակվել է 2009Artigo -
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Mapping and characterization of structural variation in 17,795 human genomes 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
Հրապարակվել է 2020Artigo -
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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects 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
Հրապարակվել է 2018Artigo -
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Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers 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
Հրապարակվել է 2016Artigo -
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Background Mutations in Parental Cells Account for Most of the Genetic Heterogeneity of Induced Pluripotent Stem Cells 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
Հրապարակվել է 2012Artigo -
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Integrated analysis of germline and somatic variants in ovarian cancer 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
Հրապարակվել է 2014Artigo -
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The Alzheimer's Disease Sequencing Project: Study design and sample selection 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
Հրապարակվել է 2017Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
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