MolBioLib: a C++11 framework for rapid development and deployment of bioinformatics tasks

por Ohsumi, Toshiro K., Borowsky, Mark L.
Publicado 2012

Functional analysis of the microtubule-interacting transcriptome

por Sharp, Judith A., Plant, Joshua J., Ohsumi, Toshiro K., Borowsky, Mark, Blower, Michael D.
Publicado 2011

Spreading of X chromosome inactivation via a hierarchy of defined Polycomb stations

por Pinter, Stefan F., Sadreyev, Ruslan I., Yildirim, Eda, Jeon, Yesu, Ohsumi, Toshiro K., Borowsky, Mark, Lee, Jeannie T.
Publicado 2012

The Microglial Sensome Revealed by Direct RNA Sequencing

por Hickman, Suzanne E., Kingery, Nathan D., Ohsumi, Toshiro, Borowsky, Mark, Wang, Li-chong, Means, Terry K., Khoury, Joseph El
Publicado 2013

Human RELA haploinsufficiency results in autosomal-dominant chronic mucocutaneous ulceration

por Badran, Yousef R., Dedeoglu, Fatma, Leyva Castillo, Juan Manuel, Bainter, Wayne, Ohsumi, Toshiro K., Bousvaros, Athos, Goldsmith, Jeffrey D., Geha, Raif S., Chou, Janet
Publicado 2017

Transposon activation mutagenesis as a screening tool for identifying resistance to cancer therapeutics

por Chen, Li, Stuart, Lynda, Ohsumi, Toshiro K, Burgess, Shawn, Varshney, Gaurav K, Dastur, Anahita, Borowsky, Mark, Benes, Cyril, Lacy-Hulbert, Adam, Schmidt, Emmett V
Publicado 2013

Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencing

por Nusbaum, Chad, Ohsumi, Toshiro K., Gomez, James, Aquadro, John, Victor, Thomas C., Warren, Robert M., Hung, Deborah T., Birren, Bruce W., Lander, Eric S., Jaffe, David B.
Publicado 2008

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

por Chiang, Colby, Jacobsen, Jessie C., Ernst, Carl, Hanscom, Carrie, Heilbut, Adrian, Blumenthal, Ian, Mills, Ryan E., Kirby, Andrew, Lindgren, Amelia M., Rudiger, Skye R., McLaughlan, Clive J., Bawden, C. Simon, Reid, Suzanne J., Faull, Richard L. M., Snell, Russell G., Hall, Ira M., Shen, Yiping, Ohsumi, Toshiro K., Borowsky, Mark L., Daly, Mark J., Lee, Charles, Morton, Cynthia C., MacDonald, Marcy E., Gusella, James F., Talkowski, Michael E.
Publicado 2012

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

por Jabara, Haifa H., Boyden, Steven E., Chou, Janet, Ramesh, Narayanaswamy, Massaad, Michel J., Benson, Halli, Bainter, Wayne, Fraulino, David, Rahimov, Fedik, Sieff, Colin, Liu, Zhi-Jian, Alshemmari, Salem H., Al-Ramadi, Basel K., Al-Dhekri, Hasan, Arnaout, Rand, Abu-Shukair, Mohammad, Vatsayan, Anant, Silver, Eli, Ahuja, Sanjay, Davies, E. Graham, Sola-Visner, Martha, Ohsumi, Toshiro K., Andrews, Nancy C., Notarangelo, Luigi D., Fleming, Mark D., Al-Herz, Waleed, Kunkel, Louis M., Geha, Raif S.
Publicado 2015