Zoekresultaten - Wheeler, David A.

From human genome to cancer genome: The first decade door Wheeler, David A., Wang, Linghua

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Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma door Wheeler, David A., Roberts, Lewis R.

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Acquired uniparental disomy of chromosome 9p in hematological malignancies door Wang, Linghua, Wheeler, David A., Prchal, Josef T.

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Prediction of Missense Mutation Functionality Depends on both the Algorithm and Sequence Alignment Employed door Hicks, Stephanie, Wheeler, David A., Plon, Sharon E., Kimmel, Marek

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A Paradigm for Electronic Publication door Steffen, David L., Yarus, Sinai, Burch, Paula E., Wheeler, David A.

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ID/HIV Physician Ambassadors: Advancing Policy to Improve Health door Brito, Maximo O, Dugdale, Caitlin M, Collins-Ogle, Michelle, Snowden, Jessica, Wheeler, David A

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Infectious Diseases/Human Immunodeficiency Virus Physician Ambassadors: Advancing Policy to Improve Health door Brito, Maximo O, Dugdale, Caitlin M, Collins-Ogle, Michelle, Snowden, Jessica, Wheeler, David A

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Framework for microRNA variant annotation and prioritization using human population and disease datasets door Oak, Ninad, Ghosh, Rajarshi, Huang, Kuan-lin, Wheeler, David A., Ding, Li, Plon, Sharon E.

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SubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization door Qiao, Yi, Quinlan, Aaron R, Jazaeri, Amir A, Verhaak, Roeland GW, Wheeler, David A, Marth, Gabor T

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Orphan Nuclear Receptor GCNF Is Required for the Repression of Pluripotency Genes during Retinoic Acid-Induced Embryonic Stem Cell Differentiation door Gu, Peili, LeMenuet, Damien, Chung, Arthur C.-K., Mancini, Michael, Wheeler, David A., Cooney, Austin J.

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Overview of the Development of Personalized Genomic Medicine and Surgery door Brunicardi, F. Charles, Gibbs, Richard A., Wheeler, David A., Nemunaitis, John, Fisher, William, Goss, John, Chen, Changyi

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Coexistence of gain-of-function JAK2 germ line mutations with JAK2(V617F) in polycythemia vera door Lanikova, Lucie, Babosova, Olga, Swierczek, Sabina, Wang, Linghua, Wheeler, David A., Divoky, Vladimir, Korinek, Vladimir, Prchal, Josef T.

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Orphan Nuclear Receptor GCNF Is Required for the Repression ofPluripotency Genes during Retinoic Acid-Induced EmbryonicStem Cell Differentiation door Gu, Peili, Le Menuet, Damien, Chung, Arthur C.-K., Mancini, Michael A., Wheeler, David A., Cooney, Austin J.

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Genome-Wide Analysis of Binding Sites and Direct Target Genes of the Orphan Nuclear Receptor NR2F1/COUP-TFI door Montemayor, Celina, Montemayor, Oscar A., Ridgeway, Alex, Lin, Feng, Wheeler, David A., Pletcher, Scott D., Pereira, Fred A.

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MuSE: accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data door Fan, Yu, Xi, Liu, Hughes, Daniel S. T., Zhang, Jianjun, Zhang, Jianhua, Futreal, P. Andrew, Wheeler, David A., Wang, Wenyi

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Dynamic Analyses of Alternative Polyadenylation from RNA-Seq Reveal 3′-UTR Landscape Across 7 Tumor Types door Xia, Zheng, Donehower, Lawrence A, Cooper, Thomas A., Neilson, Joel R., Wheeler, David A., Wagner, Eric J., Li, Wei

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RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data door Bařinka, Jan, Hu, Zunsong, Wang, Lu, Wheeler, David A., Rahbarinia, Delaram, McLeod, Clay, Gu, Zhaohui, Mullighan, Charles G.

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Web-Based Tools for Medical Education Information Management door Wheeler, David A., Steffen, David L., Deretchin, Louise F., Chapman, Jeanne Anne, Burch, Paula E., Beck, J. Robert, Jefferson, Larry S.

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ITD assembler: an algorithm for internal tandem duplication discovery from short-read sequencing data door Rustagi, Navin, Hampton, Oliver A, Li, Jie, Xi, Liu, Gibbs, Richard A., Plon, Sharon E., Kimmel, Marek, Wheeler, David A.

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Mixed Phenotype Acute Leukemia (MPAL) Exhibits Frequent Mutations in DNMT3A and Activated Signaling Genes door Eckstein, Olive S., Wang, Linghua, Punia, Jyotinder N., Kornblau, Steven M., Andreeff, Michael, Wheeler, David A., Goodell, Margaret A., Rau, Rachel E.

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