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2020 – today
- 2020
[i2]David Salgado
, Irina M. Armean, Michael Baudis, Sergi Beltran, Salvador Capella-Gutiérrez, Denise Carvalho-Silva, Victoria Dominguez Del Angel, Joaquín Dopazo, Laura I. Furlong, Bo Gao, Leyla Jael García Castro, Dietlind Gerloff, Ivo Gut, Attila Gyenesei, Nina Habermann, John M. Hancock, Marc Hanauer, Eivind Hovig, Lennart F. Johansson, Thomas Keane, Jan Korbel, Katharina B. Lauer, Steve Laurie, Brane Leskosek, David Lloyd, Tomàs Marquès-Bonet, Hailiang Mei, Katalin Monostory, Janet Piñero, Krzysztof Poterlowicz, Ana Rath, Pubudu Samarakoon, Ferran Sanz, Gary Saunders, Daoud Sie, Morris A. Swertz, Kirill Tsukanov, Alfonso Valencia, Marko Vidak, Cristina Yenyxe González, Bauke Ylstra, Christophe Béroud:
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research. F1000Research 9: 1229 (2020)
2010 – 2019
- 2019
- [j9]Jos B. Poell, Matias Mendeville, Daoud Sie, Arjen Brink, Ruud H. Brakenhoff, Bauke Ylstra:
ACE: absolute copy number estimation from low-coverage whole-genome sequencing data. Bioinform. 35(16): 2847-2849 (2019) - 2016
- [i1]Evert van den Broek, Stef van Lieshout, Christian Rausch, Bauke Ylstra, Mark A. van de Wiel, Gerrit A. Meijer, Remond J. A. Fijneman, Sanne Abeln:
GeneBreak: detection of recurrent DNA copy number aberration-associated chromosomal breakpoints within genes. F1000Research 5: 2340 (2016) - 2012
- [j8]Wessel N. van Wieringen, Kristian Unger, Gwenaël G. R. Leday, Oscar Krijgsman, Renée X. de Menezes, Bauke Ylstra, Mark A. van de Wiel:
Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses. BMC Bioinform. 13: 80 (2012) - 2011
- [j7]Mark A. van de Wiel, Franck Picard, Wessel N. van Wieringen, Bauke Ylstra:
Preprocessing and downstream analysis of microarray DNA copy number profiles. Briefings Bioinform. 12(1): 10-21 (2011) - 2010
- [j6]Ilari Scheinin, Jose A. Ferreira, Sakari Knuutila, Gerrit Meijer, Mark A. van de Wiel, Bauke Ylstra:
CGHpower: exploring sample size calculations for chromosomal copy number experiments. BMC Bioinform. 11: 331 (2010)
2000 – 2009
- 2009
- [j5]Mark A. van de Wiel, Rebecca Brosens, Paul H. C. Eilers, Candy Kumps, Gerrit Meijer, Björn Menten, Erik Sistermans, Frank Speleman, Marieke E. Timmerman, Bauke Ylstra:
Smoothing waves in array CGH tumor profiles. Bioinform. 25(9): 1099-1104 (2009) - 2007
- [j4]Mark A. van de Wiel, Kyung In Kim, Sjoerd J. Vosse, Wessel N. van Wieringen, Saskia M. Wilting, Bauke Ylstra:
CGHcall: calling aberrations for array CGH tumor profiles. Bioinform. 23(7): 892-894 (2007) - 2006
- [j3]Wessel N. van Wieringen, Jeroen A. M. Beliën, Sjoerd J. Vosse, Eskeatnaf M. Achame, Bauke Ylstra:
ACE-it: a tool for genome-wide integration of gene dosage and RNA expression data. Bioinform. 22(15): 1919-1920 (2006) - 2005
- [j2]Mark A. van de Wiel, Serge J. Smeets, Ruud H. Brakenhoff, Bauke Ylstra:
CGHMultiArray: exact P-values for multi-array comparative genomic hybridization data. Bioinform. 21(14): 3193-3194 (2005) - 2004
- [j1]Kees Jong, Elena Marchiori, Gerrit Meijer, Aad van der Vaart, Bauke Ylstra:
Breakpoint identification and smoothing of array comparative genomic hybridization data. Bioinform. 20(18): 3636-3637 (2004) - 2003
- [c1]Kees Jong, Elena Marchiori, Aad van der Vaart, Bauke Ylstra, Marjan Weiss, Gerrit Meijer:
Chromosomal Breakpoint Detection in Human Cancer. EvoWorkshops 2003: 54-65
Coauthor Index
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