نتائج البحث - Larson, David E
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VarScan: variant detection in massively parallel sequencing of individual and pooled samples حسب Koboldt, Daniel C., Chen, Ken, Wylie, Todd, Larson, David E., McLellan, Michael D., Mardis, Elaine R., Weinstock, George M., Wilson, Richard K., Ding, Li
منشور في 2009نص -
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VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing حسب Koboldt, Daniel C., Zhang, Qunyuan, Larson, David E., Shen, Dong, McLellan, Michael D., Lin, Ling, Miller, Christopher A., Mardis, Elaine R., Ding, Li, Wilson, Richard K.
منشور في 2012نص -
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SomaticSniper: identification of somatic point mutations in whole genome sequencing data حسب Larson, David E., Harris, Christopher C., Chen, Ken, Koboldt, Daniel C., Abbott, Travis E., Dooling, David J., Ley, Timothy J., Mardis, Elaine R., Wilson, Richard K., Ding, Li
منشور في 2012نص -
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Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African-Americans حسب Koboldt, Daniel C., Kanchi, Krishna L., Gui, Bin, Larson, David E., Fulton, Robert S., Isaacs, William B., Kraja, Aldi, Borecki, Ingrid B., Jia, Li, Wilson, Richard K., Mardis, Elaine R., Kibel, Adam S.
منشور في 2016نص -
14
CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data حسب Zhang, Qunyuan, Ding, Li, Larson, David E., Koboldt, Daniel C., McLellan, Michael D., Chen, Ken, Shi, Xiaoqi, Kraja, Aldi, Mardis, Elaine R., Wilson, Richard K., Borecki, Ingrid B., Province, Michael A.
منشور في 2010نص -
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Bam-readcount - rapid generation of basepair-resolution sequence metrics حسب Khanna, Ajay, Larson, David E., Srivatsan, Sridhar Nonavinkere, Mosior, Matthew, Abbott, Travis E., Kiwala, Susanna, Ley, Timothy J., Duncavage, Eric J., Walter, Matthew J., Walker, Jason R., Griffith, Obi L., Griffith, Malachi, Miller, Christopher A.
منشور في 2021نص -
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Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders حسب Koboldt, Daniel C., Larson, David E., Sullivan, Lori S., Bowne, Sara J., Steinberg, Karyn M., Churchill, Jennifer D., Buhr, Aimee C., Nutter, Nathan, Pierce, Eric A., Blanton, Susan H., Weinstock, George M., Wilson, Richard K., Daiger, Stephen P.
منشور في 2014نص -
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BreakDancer: An algorithm for high resolution mapping of genomic structural variation حسب Chen, Ken, Wallis, John W., McLellan, Michael D., Larson, David E., Kalicki, Joelle M., Pohl, Craig S., McGrath, Sean D., Wendl, Michael C., Zhang, Qunyuan, Locke, Devin P., Shi, Xiaoqi, Fulton, Robert S., Ley, Timothy J., Wilson, Richard K., Ding, Li, Mardis, Elaine R.
منشور في 2009نص -
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Mapping and characterization of structural variation in 17,795 human genomes حسب Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.
منشور في 2020نص -
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Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers حسب Miller, Christopher A., Gindin, Yevgeniy, Lu, Charles, Griffith, Obi L, Griffith, Malachi, Shen, Dong, Hoog, Jeremy, Li, Tiandao, Larson, David E., Watson, Mark, Davies, Sherri R, Hunt, Kelly, Suman, Vera J., Snider, Jacqueline, Walsh, Thomas, Colditz, Graham A., DeSchryver, Katherine, Wilson, Richard K., Mardis, Elaine R., Ellis, Matthew J.
منشور في 2016نص -
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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects حسب Regier, Allison A., Farjoun, Yossi, Larson, David E., Krasheninina, Olga, Kang, Hyun Min, Howrigan, Daniel P., Chen, Bo-Juen, Kher, Manisha, Banks, Eric, Ames, Darren C., English, Adam C., Li, Heng, Xing, Jinchuan, Zhang, Yeting, Matise, Tara, Abecasis, Goncalo R., Salerno, Will, Zody, Michael C., Neale, Benjamin M., Hall, Ira M.
منشور في 2018نص