Large-Scale Copy Number Polymorphism in the Human Genome von Sebat, Jonathan, Lakshmi, B., Troge, Jennifer, Alexander, Joan, Young, Janet, Lundin, Pär, Månér, Susanne, Massa, Hillary, Walker, Megan, Chi, Maoyen, Navin, Nicholas, Lucito, Robert, Healy, John, Hicks, James, Ye, Kenny, Reiner, Andrew, Gilliam, T. Conrad, Trask, Barbara, Patterson, Nick, Zetterberg, Anders, Wigler, Michael

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Somatic mutagenesis in satellite cells associates with human skeletal muscle aging von Franco, Irene, Johansson, Anna, Olsson, Karl, Vrtačnik, Peter, Lundin, Pär, Helgadottir, Hafdis T., Larsson, Malin, Revêchon, Gwladys, Bosia, Carla, Pagnani, Andrea, Provero, Paolo, Gustafsson, Thomas, Fischer, Helene, Eriksson, Maria

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Inferring tumor progression from genomic heterogeneity von Navin, Nicholas, Krasnitz, Alexander, Rodgers, Linda, Cook, Kerry, Meth, Jennifer, Kendall, Jude, Riggs, Michael, Eberling, Yvonne, Troge, Jennifer, Grubor, Vladimir, Levy, Dan, Lundin, Pär, Månér, Susanne, Zetterberg, Anders, Hicks, James, Wigler, Michael

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Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type von Franco, Irene, Helgadottir, Hafdis T, Moggio, Aldo, Larsson, Malin, Vrtačnik, Peter, Johansson, Anna, Norgren, Nina, Lundin, Pär, Mas-Ponte, David, Nordström, Johan, Lundgren, Torbjörn, Stenvinkel, Peter, Wennberg, Lars, Supek, Fran, Eriksson, Maria

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SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population von Ameur, Adam, Dahlberg, Johan, Olason, Pall, Vezzi, Francesco, Karlsson, Robert, Martin, Marcel, Viklund, Johan, Kähäri, Andreas Kusalananda, Lundin, Pär, Che, Huiwen, Thutkawkorapin, Jessada, Eisfeldt, Jesper, Lampa, Samuel, Dahlberg, Mats, Hagberg, Jonas, Jareborg, Niclas, Liljedahl, Ulrika, Jonasson, Inger, Johansson, Åsa, Feuk, Lars, Lundeberg, Joakim, Syvänen, Ann-Christine, Lundin, Sverker, Nilsson, Daniel, Nystedt, Björn, Magnusson, Patrik Ke, Gyllensten, Ulf

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A novel RNA sequencing data analysis method for cell line authentication von Fasterius, Erik, Raso, Cinzia, Kennedy, Susan, Rauch, Nora, Lundin, Pär, Kolch, Walter, Uhlén, Mathias, Al-Khalili Szigyarto, Cristina

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Somatic mutation that affects transcription factor binding upstream of CD55 in the temporal cortex of a late-onset Alzheimer disease patient von Helgadottir, Hafdis T, Lundin, Pär, Wallén Arzt, Emelie, Lindström, Anna-Karin, Graff, Caroline, Eriksson, Maria

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Novel patterns of genome rearrangement and their association with survival in breast cancer von Hicks, James, Krasnitz, Alexander, Lakshmi, B, Navin, Nicholas E, Riggs, Michael, Leibu, Evan, Esposito, Diane, Alexander, Joan, Troge, Jen, Grubor, Vladimir, Yoon, Seungtai, Wigler, Michael, Ye, Kenny, Børresen-Dale, Anne-Lise, Naume, Bjørn, Schlicting, Ellen, Norton, Larry, Hägerström, Torsten, Skoog, Lambert, Auer, Gert, Månér, Susanne, Lundin, Pär, Zetterberg, Anders

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Genomic architecture characterizes tumor progression paths and fate in breast cancer patients von Russnes, HG, Vollan, HKM, Lingjaerde, OC, Krasnitz, A, Lundin, P, Naume, B, Sorlie, T, Borgen, E, Rye, IH, Langerod, A, Chin, SF, Teschendorff, AE, Stephens, PJ, Maner, S, Schlichting, E, Baumbusch, LO, Karesen, R, Stratton, MP, Wigler, M, Caldas, C, Zetterberg, A, Hicks, J, Borresen-Dale, AL

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Linkage and whole genome sequencing identify a locus on 6q25–26 for formal thought disorder and implicate MEF2A regulation von Thygesen, Johan Hilge, Zambach, Sine Katharina, Ingason, Andrés, Lundin, Pär, Hansen, Thomas, Bertalan, Marcelo, Rosengren, Anders, Bjerre, Ditte, Ferrero-Miliani, Laura, Rasmussen, Henrik Berg, Parnas, Josef, Werge, Thomas

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Quantitative multigene FISH on breast carcinomas identifies der(1;16)(q10;p10) as an early event in luminal A tumors von Rye, Inga H., Lundin, Pär, Månér, Susanne, Fjelldal, Renathe, Naume, Bjørn, Wigler, Michael, Hicks, James, Børresen-Dale, Anne-Lise, Zetterberg, Anders, Russnes, Hege G.

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PROBER: oligonucleotide FISH probe design software von Navin, Nicholas, Grubor, Vladimir, Hicks, Jim, Leibu, Evan, Thomas, Elizabeth, Troge, Jennifer, Riggs, Michael, Lundin, Pär, Månér, Susanne, Sebat, Jonathan, Zetterberg, Anders, Wigler, Michael

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Mutations in BRIP1 confer high risk of ovarian cancer von Rafnar, Thorunn, Stefansson, Kari, Gudbjartsson, Daniel F, Sulem, Patrick, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Besenbacher, Soren, Lundin, Pär, Stacey, Simon N, Gudmundsson, Julius, Magnusson, Olafur T, le Roux, Louise, Orlygsdottir, Gudbjorg, Helgadottir, Hafdis T, Johannsdottir, Hrefna, Gylfason, Arnaldur, Tryggvadottir, Laufey, Jonasson, Jon G, de Juan, Ana, Ortega, Eugenia, Ramon-Cajal, Jose M, García-Prats, Maria D, Mayordomo, Carlos, Panadero, Angeles, Rivera, Fernando, Aben, Katja K H, van Altena, Anne M, Massuger, Leon F A G, Aavikko, Mervi, Kujala, Paula M, Staff, Synnöve, Aaltonen, Lauri A, Olafsdottir, Kristrun, Bjornsson, Johannes, Kong, Augustine, Salvarsdottir, Anna, Saemundsson, Hafsteinn, Olafsson, Karl, Benediktsdottir, Kristrun R, Gulcher, Jeffrey, Masson, Gisli, Kiemeney, Lambertus A, Mayordomo, Jose I, Thorsteinsdottir, Unnur

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SO042WHOLE GENOME SEQUENCING OF HUMAN KIDNEY PROGENITORS IDENTIFIES A MUTATION-PRONE CELL TYPE IN THE PROXIMAL TUBULE von Franco, Irene, Helgadottir, Hafdis, Moggio, Aldo, Larsson, Malin, Vrtacnik, Peter, Johansson, Anna, Norgren, Nina, Lundin, Pär, Mas-Ponte, David, Nordstrom, Johan, Lundgren, Torbjörn, Stenvinkel, Peter, Wennberg, Lars, Supek, Fran, Eriksson, Maria

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SO042WHOLE GENOME SEQUENCING OF HUMAN KIDNEY PROGENITORS IDENTIFIES A MUTATION-PRONE CELL TYPE IN THE PROXIMAL TUBULE von Franco, Irene, Helgadottir, Hafdis, Moggio, Aldo, Larsson, Malin, Vrtacnik, Peter, Johansson, Anna, Norgren, Nina, Lundin, Pär, Mas-Ponte, David, Nordstrom, Johan, Lundgren, Torbjörn, Stenvinkel, Peter, Wennberg, Lars, Supek, Fran, Eriksson, Maria

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Analysis of chromosomal rearrangements and gene copy number changes in breast cancer cells von Lundin, Pär

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MOESM3 of Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type von Franco, Irene, Hafdis Helgadottir, Moggio, Aldo, Larsson, Malin, Vrtačnik, Peter, Johansson, Anna, Norgren, Nina, Lundin, Pär, Mas-Ponte, David, Nordström, Johan, Lundgren, Torbjörn, Stenvinkel, Peter, Wennberg, Lars, Supek, Fran, Eriksson, Maria

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MOESM2 of Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type von Franco, Irene, Hafdis Helgadottir, Moggio, Aldo, Larsson, Malin, Vrtačnik, Peter, Johansson, Anna, Norgren, Nina, Lundin, Pär, Mas-Ponte, David, Nordström, Johan, Lundgren, Torbjörn, Stenvinkel, Peter, Wennberg, Lars, Supek, Fran, Eriksson, Maria

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Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type von Franco, Irene, Helgadottir, Hafdis T, Moggio, Aldo, Larsson, Malin, Vrtacnik, Peter, Johansson, Anna C. V, Norgren, Nina, Lundin, Par, Mas-Ponte, David, Nordstrom, Johan, Lundgren, Torbjorn, Stenvinkel, Peter, Wennberg, Lars, Supek, Fran, Eriksson, Maria

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Somatic mutagenesis in satellite cells associates with human skeletal muscle aging von Franco, Irene, Johansson, Anna C. V, Olsson, Karl, Vrtacnik, Peter, Lundin, Par, Helgadottir, Hafdis T, Larsson, Malin, Revechon, Gwladys, Bosia, Carla, Pagnani, Andrea, Provero, Paolo, Gustafsson, Thomas, Fischer, Helene, Eriksson, Maria

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