Хайлтын үр дүнгүүд - Larson, David E
- 49-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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VarScan: variant detection in massively parallel sequencing of individual and pooled samples -н Koboldt, Daniel C., Chen, Ken, Wylie, Todd, Larson, David E., McLellan, Michael D., Mardis, Elaine R., Weinstock, George M., Wilson, Richard K., Ding, Li
Хэвлэсэн 2009текст -
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VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing -н 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.
Хэвлэсэн 2012текст -
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SomaticSniper: identification of somatic point mutations in whole genome sequencing data -н 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
Хэвлэсэн 2012текст -
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Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African-Americans -н 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.
Хэвлэсэн 2016текст -
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CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data -н 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.
Хэвлэсэн 2010текст -
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Bam-readcount - rapid generation of basepair-resolution sequence metrics -н 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.
Хэвлэсэн 2021текст -
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Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders -н 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.
Хэвлэсэн 2014текст -
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BreakDancer: An algorithm for high resolution mapping of genomic structural variation -н 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.
Хэвлэсэн 2009текст -
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Mapping and characterization of structural variation in 17,795 human genomes -н 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.
Хэвлэсэн 2020текст -
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Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers -н 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.
Хэвлэсэн 2016текст -
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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects -н 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.
Хэвлэсэн 2018текст