Výsledky vyhledávání - Luquette, Lovelace J

Somatic mutation accumulation seen through a single-molecule lens Autor Luquette, Lovelace J., Park, Peter J.

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Estimating enrichment of repetitive elements from high-throughput sequence data Autor Day, Daniel S, Luquette, Lovelace J, Park, Peter J, Kharchenko, Peter V

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rSW-seq: Algorithm for detection of copy number alterations in deep sequencing data Autor Kim, Tae-Min, Luquette, Lovelace J, Xi, Ruibin, Park, Peter J

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Detecting somatic mutations in normal cells Autor Dou, Yanmei, Gold, Heather D., Luquette, Lovelace J., Park, Peter J.

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Identification of somatic mutations in single cell DNA-seq using a spatial model of allelic imbalance Autor Luquette, Lovelace J., Bohrson, Craig L., Sherman, Max A., Park, Peter J.

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Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes Autor Kim, Tae-Min, Xi, Ruibin, Luquette, Lovelace J., Park, Richard W., Johnson, Mark D., Park, Peter J.

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COSMOS: Python library for massively parallel workflows Autor Gafni, Erik, Luquette, Lovelace J., Lancaster, Alex K., Hawkins, Jared B., Jung, Jae-Yoon, Souilmi, Yassine, Wall, Dennis P., Tonellato, Peter J.

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Systematic Identification of Synergistic Drug Pairs Targeting HIV Autor Tan, Xu, Hu, Long, Luquette, Lovelace J., Gao, Geng, Liu, Yifang, Qu, Hongjing, Xi, Ruibin, Lu, Zhi John, Park, Peter J., Elledge, Stephen J.

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Accurate detection of mosaic variants in sequencing data without matched controls Autor Dou, Yanmei, Kwon, Minseok, Rodin, Rachel E., Cortés-Ciriano, Isidro, Doan, Ryan, Luquette, Lovelace J., Galor, Alon, Bohrson, Craig, Walsh, Christopher A., Park, Peter J.

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Diverse mechanisms of somatic structural variations in human cancer genomes Autor Yang, Lixing, Luquette, Lovelace J., Gehlenborg, Nils, Xi, Ruibin, Haseley, Psalm S., Hsieh, Chih-Heng, Zhang, Chengsheng, Ren, Xiaojia, Protopopov, Alexei, Chin, Lynda, Kucherlapati, Raju, Lee, Charles, Park, Peter J.

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Impact of sequencing depth in ChIP-seq experiments Autor Jung, Youngsook L., Luquette, Lovelace J., Ho, Joshua W.K., Ferrari, Francesco, Tolstorukov, Michael, Minoda, Aki, Issner, Robbyn, Epstein, Charles B., Karpen, Gary H., Kuroda, Mitzi I., Park, Peter J.

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Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion Autor Xi, Ruibin, Hadjipanayis, Angela G., Luquette, Lovelace J., Kim, Tae-Min, Lee, Eunjung, Zhang, Jianhua, Johnson, Mark D., Muzny, Donna M., Wheeler, David A., Gibbs, Richard A., Kucherlapati, Raju, Park, Peter J.

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Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition Autor Brownstein, Catherine A., Towne, Meghan C., Luquette, Lovelace J., Harris, David J., Marinakis, Nicholas S., Meinecke, Peter, Kutsche, Kerstin, Campeau, Philippe M., Yu, Timothy W., Margulies, David M., Agrawal, Pankaj B., Beggs, Alan H.

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Linked-read analysis identifies mutations in single-cell DNA sequencing data Autor Bohrson, Craig L., Barton, Alison R., Lodato, Michael A., Rodin, Rachel E., Luquette, Lovelace J., Viswanadham, Vinay, Gulhan, Doga C., Cortés-Ciriano, Isidro, Sherman, Maxwell A., Kwon, Minseok, Coulter, Michael E., Galor, Alon, Walsh, Christopher A., Park, Peter J.

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Analysis of somatic retrotransposition in human cancers Autor Lee, Eunjung, Iskow, Rebecca, Yang, Lixing, Gokcumen, Omer, Haseley, Psalm, Luquette, Lovelace J, Lohr, Jens G, Harris, Christopher C, Ding, Li, Wilson, Richard K, Wheeler, David A, Gibbs, Richard A, Kucherlapati, Raju, Lee, Charles, Kharchenko, Peter V, Park, Peter J

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Landscape of Somatic Retrotransposition in Human Cancers Autor Lee, Eunjung, Iskow, Rebecca, Yang, Lixing, Gokcumen, Omer, Haseley, Psalm, Luquette, Lovelace J., Lohr, Jens G., Harris, Christopher C., Ding, Li, Wilson, Richard K., Wheeler, David A., Gibbs, Richard A., Kucherlapati, Raju, Lee, Charles, Kharchenko, Peter V., Park, Peter J.

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Orthogonal NGS for High Throughput Clinical Diagnostics Autor Chennagiri, Niru, White, Eric J., Frieden, Alexander, Lopez, Edgardo, Lieber, Daniel S., Nikiforov, Anastasia, Ross, Tristen, Batorsky, Rebecca, Hansen, Sherry, Lip, Va, Luquette, Lovelace J., Mauceli, Evan, Margulies, David, Milos, Patrice M., Napolitano, Nichole, Nizzari, Marcia M., Yu, Timothy, Thompson, John F.

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The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing Autor Rodin, Rachel E., Dou, Yanmei, Kwon, Minseok, Sherman, Maxwell A., D’Gama, Alissa M., Doan, Ryan N., Rento, Lariza M., Girskis, Kelly M., Bohrson, Craig L., Kim, Sonia N., Nadig, Ajay, Luquette, Lovelace J., Gulhan, Doga C., Park, Peter J., Walsh, Christopher A.

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Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing Autor Rodin, Rachel E., Dou, Yanmei, Kwon, Minseok, Sherman, Maxwell A., D’Gama, Alissa M., Doan, Ryan N., Rento, Lariza M., Girskis, Kelly M., Bohrson, Craig L., Kim, Sonia N., Nadig, Ajay, Luquette, Lovelace J., Gulhan, Doga C., Park, Peter J., Walsh, Christopher A.

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Aging and neurodegeneration are associated with increased mutations in single human neurons Autor Lodato, Michael A., Rodin, Rachel E., Bohrson, Craig L., Coulter, Michael E., Barton, Alison R., Kwon, Minseok, Sherman, Maxwell A., Vitzthum, Carl M., Luquette, Lovelace J., Yandava, Chandri N., Yang, Pengwei, Chittenden, Thomas W., Hatem, Nicole E., Ryu, Steven C., Woodworth, Mollie B., Park, Peter J., Walsh, Christopher A.

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