Zoekresultaten - Kloosterman, Wigard P.
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MicroRNAs show a wide diversity of expression profiles in the developing and mature central nervous system door Kapsimali, Marika, Kloosterman, Wigard P, de Bruijn, Ewart, Rosa, Frederic, Plasterk, Ronald HA, Wilson, Stephen W
Gepubliceerd in 2007Text -
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sv-callers: a highly portable parallel workflow for structural variant detection in whole-genome sequence data door Kuzniar, Arnold, Maassen, Jason, Verhoeven, Stefan, Santuari, Luca, Shneider, Carl, Kloosterman, Wigard P., de Ridder, Jeroen
Gepubliceerd in 2020Text -
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ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation door Sante, Tom, Vergult, Sarah, Volders, Pieter-Jan, Kloosterman, Wigard P., Trooskens, Geert, De Preter, Katleen, Dheedene, Annelies, Speleman, Frank, De Meyer, Tim, Menten, Björn
Gepubliceerd in 2014Text -
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Development of a Personalized Tumor Neoantigen Based Vaccine Formulation (FRAME-001) for Use in a Phase II Trial for the Treatment of Advanced Non-Small Cell Lung Cancer door Oosting, Linette T., Franke, Katka, Martin, Michael V., Kloosterman, Wigard P., Jamieson, Jennifer A., Glenn, Laura A., de Jager, Miranda W., van Zanten, Jacoba, Allersma, Derk P., Gareb, Bahez
Gepubliceerd in 2022Text -
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Improving mammalian genome scaffolding using large insert mate-pair next-generation sequencing door van Heesch, Sebastiaan, Kloosterman, Wigard P, Lansu, Nico, Ruzius, Frans-Paul, Levandowsky, Elizabeth, Lee, Clarence C, Zhou, Shiguo, Goldstein, Steve, Schwartz, David C, Harkins, Timothy T, Guryev, Victor, Cuppen, Edwin
Gepubliceerd in 2013Text -
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Same-day genomic and epigenomic diagnosis of brain tumors using real-time nanopore sequencing door Euskirchen, Philipp, Bielle, Franck, Labreche, Karim, Kloosterman, Wigard P., Rosenberg, Shai, Daniau, Mailys, Schmitt, Charlotte, Masliah-Planchon, Julien, Bourdeaut, Franck, Dehais, Caroline, Marie, Yannick, Delattre, Jean-Yves, Idbaih, Ahmed
Gepubliceerd in 2017Text -
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Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring door de Pagter, Mirjam S., van Roosmalen, Markus J., Baas, Annette F., Renkens, Ivo, Duran, Karen J., van Binsbergen, Ellen, Tavakoli-Yaraki, Masoumeh, Hochstenbach, Ron, van der Veken, Lars T., Cuppen, Edwin, Kloosterman, Wigard P.
Gepubliceerd in 2015Text -
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A framework for the detection of de novo mutations in family-based sequencing data door Francioli, Laurent C, Cretu-Stancu, Mircea, Garimella, Kiran V, Fromer, Menachem, Kloosterman, Wigard P, Samocha, Kaitlin E, Neale, Benjamin M, Daly, Mark J, Banks, Eric, DePristo, Mark A, de Bakker, Paul IW
Gepubliceerd in 2017Text -
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Mouse microRNA profiles determined with a new and sensitive cloning method door Takada, Shuji, Berezikov, Eugene, Yamashita, Yoshihiro, Lagos-Quintana, Mariana, Kloosterman, Wigard P., Enomoto, Munehiro, Hatanaka, Hisashi, Fujiwara, Shin-ichiro, Watanabe, Hideki, Soda, Manabu, Choi, Young Lim, Plasterk, Ronald H. A., Cuppen, Edwin, Mano, Hiroyuki
Gepubliceerd in 2006Text -
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Micronuclei-based model system reveals functional consequences of chromothripsis in human cells door Kneissig, Maja, Keuper, Kristina, de Pagter, Mirjam S, van Roosmalen, Markus J, Martin, Jana, Otto, Hannah, Passerini, Verena, Campos Sparr, Aline, Renkens, Ivo, Kropveld, Fenna, Vasudevan, Anand, Sheltzer, Jason M, Kloosterman, Wigard P, Storchova, Zuzana
Gepubliceerd in 2019Text -
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Discovery of variants unmasked by hemizygous deletions door Hochstenbach, Ron, Poot, Martin, Nijman, Isaac J, Renkens, Ivo, Duran, Karen J, van'T Slot, Ruben, van Binsbergen, Ellen, van der Zwaag, Bert, Vogel, Maartje J, Terhal, Paulien A, Ploos van Amstel, Hans Kristian, Kloosterman, Wigard P, Cuppen, Edwin
Gepubliceerd in 2012Text