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2010 – 2019
- 2018
[j4]Paul Deveau, Leo Colmet Daage
, Derek Oldridge, Virginie Bernard, Angela Bellini, Mathieu Chicard, Nathalie Clement, Eve Lapouble, Valerie Combaret, Anne Boland, Vincent Meyer, Jean-Francois Deleuze, Isabelle Janoueix-Lerosey, Emmanuel Barillot, Olivier Delattre, John M. Maris, Gudrun Schleiermacher, Valentina Boeva:
QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction. Bioinform. 34(11): 1808-1816 (2018)- 2016
- [c2]Hubert Ebner, Dieter Hayn, Markus Falgenhauer, Michael Nitzlnader, Gudrun Schleiermacher, Riccardo Haupt, Giovanni Erminio, Raffaella Defferrari, Katia Mazzocco, Jan Kohler, Gian Paolo Tonini, Ruth Ladenstein, Günter Schreier:
Piloting the European Unified Patient Identity Management (EUPID) Concept to Facilitate Secondary Use of Neuroblastoma Data from Clinical Trials and Biobanking. eHealth 2016: 31-38 - [c1]Dieter Hayn, Markus Falgenhauer, Martin Kropf, Michael Nitzlnader, Stefan Welte, Hubert Ebner, Ruth Ladenstein, Gudrun Schleiermacher, Barbara Hero, Günter Schreier:
IT Infrastructure for Merging Data from Different Clinical Trials and Across Independent Research Networks. MIE 2016: 287-291 - 2014
- [j3]Toby Dylan Hocking, Valentina Boeva, Guillem Rigaill, Gudrun Schleiermacher, Isabelle Janoueix-Lerosey, Olivier Delattre, Wilfrid Richer, Franck Bourdeaut, Miyuki Suguro, Masao Seto, Francis R. Bach, Jean-Philippe Vert:
SegAnnDB: interactive Web-based genomic segmentation. Bioinform. 30(11): 1539-1546 (2014) - 2013
- [j2]Toby Dylan Hocking, Gudrun Schleiermacher, Isabelle Janoueix-Lerosey, Valentina Boeva, Julie Cappo, Olivier Delattre, Francis R. Bach, Jean-Philippe Vert:
Learning smoothing models of copy number profiles using breakpoint annotations. BMC Bioinform. 14: 164 (2013) - 2012
- [j1]Valentina Boeva, Tatiana G. Popova, Kevin Bleakley, Pierre Chiche, Julie Cappo, Gudrun Schleiermacher, Isabelle Janoueix-Lerosey, Olivier Delattre, Emmanuel Barillot:
Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data. Bioinform. 28(3): 423-425 (2012)
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