Bauke Ylstra

According to our database, Bauke Ylstra authored at least 12 papers between 2003 and 2020.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2020

The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.

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

F1000Research, 2020

2019

ACE: absolute copy number estimation from low-coverage whole-genome sequencing data.

Jos B. Poell, Matias Mendeville, Daoud Sie, Arjen Brink, Ruud H. Brakenhoff, Bauke Ylstra

Bioinform., 2019

2016

GeneBreak: detection of recurrent DNA copy number aberration-associated chromosomal breakpoints within genes.

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

F1000Research, 2016

2012

Matching of array CGH and gene expression microarray features for the purpose of integrative genomic analyses.

Wessel N. van Wieringen, Kristian Unger, Gwenaël G. R. Leday, Oscar Krijgsman, Renée X. de Menezes, Bauke Ylstra, Mark A. van de Wiel

BMC Bioinform., 2012

2011

Preprocessing and downstream analysis of microarray DNA copy number profiles.

Mark A. van de Wiel, Franck Picard, Wessel N. van Wieringen, Bauke Ylstra

Briefings Bioinform., 2011

2010

CGHpower: exploring sample size calculations for chromosomal copy number experiments.

Ilari Scheinin, Jose A. Ferreira, Sakari Knuutila, Gerrit Meijer, Mark A. van de Wiel, Bauke Ylstra

BMC Bioinform., 2010

2009

Smoothing waves in array CGH tumor profiles.

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

Bioinform., 2009

2007

CGHcall: calling aberrations for array CGH tumor profiles.

Mark A. van de Wiel, Kyung In Kim, Sjoerd J. Vosse, Wessel N. van Wieringen, Saskia M. Wilting, Bauke Ylstra

Bioinform., 2007

2006

ACE-it: a tool for genome-wide integration of gene dosage and RNA expression data.

Wessel N. van Wieringen, Jeroen A. M. Beliën, Sjoerd J. Vosse, Eskeatnaf M. Achame, Bauke Ylstra

Bioinform., 2006

2005

CGHMultiArray: exact P-values for multi-array comparative genomic hybridization data.

Mark A. van de Wiel, Serge J. Smeets, Ruud H. Brakenhoff, Bauke Ylstra

Bioinform., 2005

2004

Breakpoint identification and smoothing of array comparative genomic hybridization data.

Kees Jong, Elena Marchiori, Gerrit Meijer, Aad van der Vaart, Bauke Ylstra

Bioinform., 2004

2003

Chromosomal Breakpoint Detection in Human Cancer.

Kees Jong, Elena Marchiori, Aad van der Vaart, Bauke Ylstra, Marjan Weiss, Gerrit Meijer

Proceedings of the Applications of Evolutionary Computing, 2003