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Gerrit Meijer
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2010 – 2019
- 2017
- [i3]Chao Zhang, Jochem Bijlard, Christine Staiger, Serena A. Scollen
, David van Enckevort
Systematically linking tranSMART, Galaxy and EGA for reusing human translational research data. F1000Research 6: 1488- (2017) - 2016
- [i2]Evert van den Broek, Stef van Lieshout, Christian Rausch, Bauke Ylstra
GeneBreak: detection of recurrent DNA copy number aberration-associated chromosomal breakpoints within genes. F1000Research 5: 2340 (2016) - [i1]Youri Hoogstrate
Integration of EGA secure data access into Galaxy. F1000Research 5: 2841 (2016) - 2015
- [j7]Askar Obulkasim, Gerrit A. Meijer
Semi-supervised adaptive-height snipping of the hierarchical clustering tree. BMC Bioinform. 16: 15:1-15:11 (2015) - [j6]Marinel Cavelaars, Jacob Rousseau, Cuneyt Parlayan, Sander de Ridder, Annemarie Verburg, Ruud Ross, Gerben Visser, Annelies Rotte, Rita Azevedo
OpenClinica. J. Clin. Bioinform. 5(S-1): S2 (2015) - [j5]Mariska Bierkens, Wim van der Linden, Kees van Bochove
tranSMART. J. Clin. Bioinform. 5(S-1): S9 (2015) - 2011
- [j4]Askar Obulkasim, Gerrit Meijer
Stepwise classification of cancer samples using clinical and molecular Data. BMC Bioinform. 12: 422 (2011) - 2010
- [j3]Ilari Scheinin, Jose A. Ferreira, Sakari Knuutila, Gerrit Meijer
CGHpower: exploring sample size calculations for chromosomal copy number experiments. BMC Bioinform. 11: 331 (2010)
2000 – 2009
- 2009
- [j2]Mark A. van de Wiel
Smoothing waves in array CGH tumor profiles. Bioinform. 25(9): 1099-1104 (2009) - 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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