Bilaketaren emaitzak - Luquette, Lovelace J

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

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Estimating enrichment of repetitive elements from high-throughput sequence data nork 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 nork Kim, Tae-Min, Luquette, Lovelace J, Xi, Ruibin, Park, Peter J

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Detecting somatic mutations in normal cells nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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 nork 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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