Hasil Pencarian - Paz Polak

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  1. 1
    APOBEC-Induced Cancer Mutations Are Uniquely Enriched in Early-Replicating, Gene-Dense, and Active Chromatin Regions

    APOBEC-Induced Cancer Mutations Are Uniquely Enriched in Early-Replicating, Gene-Dense, and Active Chromatin Regions oleh Marat D. Kazanov, Steven A. Roberts, Paz Polak, John Stamatoyannopoulos, Leszek J. Klimczak, Dmitry A. Gordenin, Shamil R. Sunyaev

    Diterbitkan 2015-11-01
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  2. 2
    The Great Majority of Homologous Recombination Repair-Deficient Tumors Are Accounted for by Established Causes

    The Great Majority of Homologous Recombination Repair-Deficient Tumors Are Accounted for by Established Causes oleh Paula Štancl, Nancy Hamel, Keith M. Sigel, William D. Foulkes, William D. Foulkes, William D. Foulkes, Rosa Karlić, Paz Polak

    Diterbitkan 2022-06-01
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  3. 3
    COOBoostR: An Extreme Gradient Boosting-Based Tool for Robust Tissue or Cell-of-Origin Prediction of Tumors

    COOBoostR: An Extreme Gradient Boosting-Based Tool for Robust Tissue or Cell-of-Origin Prediction of Tumors oleh Sungmin Yang, Kyungsik Ha, Woojeung Song, Masashi Fujita, Kirsten Kübler, Paz Polak, Eiso Hiyama, Hidewaki Nakagawa, Hong-Gee Kim, Hwajin Lee

    Diterbitkan 2022-12-01
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  4. 4
    Somatic mutation landscape reveals differential variability of cell-of-origin for primary liver cancer

    Somatic mutation landscape reveals differential variability of cell-of-origin for primary liver cancer oleh Kyungsik Ha, Masashi Fujita, Rosa Karlić, Sungmin Yang, Ruidong Xue, Chong Zhang, Fan Bai, Ning Zhang, Yujin Hoshida, Paz Polak, Hidewaki Nakagawa, Hong-Gee Kim, Hwajin Lee

    Diterbitkan 2020-02-01
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  5. 5
    A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

    A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns oleh Wei Jiao, Gurnit Atwal, Paz Polak, Rosa Karlic, Edwin Cuppen, PCAWG Tumor Subtypes and Clinical Translation Working Group, Alexandra Danyi, Jeroen de Ridder, Carla van Herpen, Martijn P. Lolkema, Neeltje Steeghs, Gad Getz, Quaid Morris, Lincoln D. Stein, PCAWG Consortium

    Diterbitkan 2020-02-01
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  6. 6
    Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer families

    Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer families oleh Thibaut S. Matis, Nadia Zayed, Bouchra Labraki, Manon de Ladurantaye, Théophane A. Matis, José Camacho Valenzuela, Nancy Hamel, Adrienne Atayan, Barbara Rivera, Yuval Tabach, Patricia N. Tonin, Alexandre Orthwein, Anne-Marie Mes-Masson, Zaki El Haffaf, William D. Foulkes, Paz Polak

    Diterbitkan 2021-08-01
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  7. 7
    Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

    Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns oleh Wei Jiao, Gurnit Atwal, Paz Polak, Rosa Karlic, Edwin Cuppen, PCAWG Tumor Subtypes and Clinical Translation Working Group, Alexandra Danyi, Jeroen de Ridder, Carla van Herpen, Martijn P. Lolkema, Neeltje Steeghs, Gad Getz, Quaid D. Morris, Lincoln D. Stein, PCAWG Consortium

    Diterbitkan 2022-12-01
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  8. 8
    Characterization of genetic predisposition to molecular subtypes of breast cancer in Brazilian patients

    Characterization of genetic predisposition to molecular subtypes of breast cancer in Brazilian patients oleh Daniele Paixão, Giovana Tardin Torrezan, Giovana Tardin Torrezan, Karina Miranda Santiago, Maria Nirvana Formiga, Samuel Terkper Ahuno, Emmanuel Dias-Neto, Emmanuel Dias-Neto, Israel Tojal da Silva, Israel Tojal da Silva, William D. Foulkes, Paz Polak, Dirce Maria Carraro, Dirce Maria Carraro

    Diterbitkan 2022-08-01
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  9. 9
    Author Correction: A framework for clinical cancer subtyping from nucleosome profiling of cell-free DNA

    Author Correction: A framework for clinical cancer subtyping from nucleosome profiling of cell-free DNA oleh Anna-Lisa Doebley, Minjeong Ko, Hanna Liao, A. Eden Cruikshank, Katheryn Santos, Caroline Kikawa, Joseph B. Hiatt, Robert D. Patton, Navonil De Sarkar, Katharine A. Collier, Anna C. H. Hoge, Katharine Chen, Anat Zimmer, Zachary T. Weber, Mohamed Adil, Jonathan B. Reichel, Paz Polak, Viktor A. Adalsteinsson, Peter S. Nelson, David MacPherson, Heather A. Parsons, Daniel G. Stover, Gavin Ha

    Diterbitkan 2023-01-01
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  10. 10
    A framework for clinical cancer subtyping from nucleosome profiling of cell-free DNA

    A framework for clinical cancer subtyping from nucleosome profiling of cell-free DNA oleh Anna-Lisa Doebley, Minjeong Ko, Hanna Liao, A. Eden Cruikshank, Katheryn Santos, Caroline Kikawa, Joseph B. Hiatt, Robert D. Patton, Navonil De Sarkar, Katharine A. Collier, Anna C. H. Hoge, Katharine Chen, Anat Zimmer, Zachary T. Weber, Mohamed Adil, Jonathan B. Reichel, Paz Polak, Viktor A. Adalsteinsson, Peter S. Nelson, David MacPherson, Heather A. Parsons, Daniel G. Stover, Gavin Ha

    Diterbitkan 2022-12-01
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  11. 11
    Circulating tumor DNA is readily detectable among Ghanaian breast cancer patients supporting non-invasive cancer genomic studies in Africa

    Circulating tumor DNA is readily detectable among Ghanaian breast cancer patients supporting non-invasive cancer genomic studies in Africa oleh Samuel Terkper Ahuno, Anna-Lisa Doebley, Thomas U. Ahearn, Joel Yarney, Nicholas Titiloye, Nancy Hamel, Ernest Adjei, Joe-Nat Clegg-Lamptey, Lawrence Edusei, Baffour Awuah, Xiaoyu Song, Verna Vanderpuye, Mustapha Abubakar, Maire Duggan, Daniel G. Stover, Kofi Nyarko, John M. S. Bartlett, Francis Aitpillah, Daniel Ansong, Kevin L. Gardner, Felix Andy Boateng, Anne M. Bowcock, Carlos Caldas, William D. Foulkes, Seth Wiafe, Beatrice Wiafe-Addai, Montserrat Garcia-Closas, Alexander Kwarteng, Gavin Ha, Jonine D. Figueroa, Paz Polak, the Ghana Breast Health Study Team

    Diterbitkan 2021-09-01
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  12. 12
    Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors

    Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors oleh Viktor A. Adalsteinsson, Gavin Ha, Samuel S. Freeman, Atish D. Choudhury, Daniel G. Stover, Heather A. Parsons, Gregory Gydush, Sarah C. Reed, Denisse Rotem, Justin Rhoades, Denis Loginov, Dimitri Livitz, Daniel Rosebrock, Ignaty Leshchiner, Jaegil Kim, Chip Stewart, Mara Rosenberg, Joshua M. Francis, Cheng-Zhong Zhang, Ofir Cohen, Coyin Oh, Huiming Ding, Paz Polak, Max Lloyd, Sairah Mahmud, Karla Helvie, Margaret S. Merrill, Rebecca A. Santiago, Edward P. O’Connor, Seong H. Jeong, Rachel Leeson, Rachel M. Barry, Joseph F. Kramkowski, Zhenwei Zhang, Laura Polacek, Jens G. Lohr, Molly Schleicher, Emily Lipscomb, Andrea Saltzman, Nelly M. Oliver, Lori Marini, Adrienne G. Waks, Lauren C. Harshman, Sara M. Tolaney, Eliezer M. Van Allen, Eric P. Winer, Nancy U. Lin, Mari Nakabayashi, Mary-Ellen Taplin, Cory M. Johannessen, Levi A. Garraway, Todd R. Golub, Jesse S. Boehm, Nikhil Wagle, Gad Getz, J. Christopher Love, Matthew Meyerson

    Diterbitkan 2017-11-01
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