Risultati finali
Opensource software supporting the molecular tumour characterization pipeline and predicting perturbed pathways
Software package for automated benchmarkingOpen-source software with updated Renjin and code library of benchmarks and technical report describing most significant performance bottlenecks
Opensource software implementing an updated version of Renjin that supports the major Bioconductor packages a code library of benchmarks and a technical report describing the most significant performance bottlenecks
Open-source software CAUSEXPR, to prioritize likely causal mutations from genotype and gene expressionOpen-source software CAUSEXPR to prioritize likely causal mutations from genotype and gene expression
Open-source software that implements tumour diversity time series analysisTechnical report and software for predictive modelling of drug response and detection of outlier samples
Technical report and accompanying open-source software for predictive modelling of drug response and detection of outlier samples in lymphomas and leukaemias.
Open-source software CAUSAMET and BIOMARKOpen-source software CAUSAMET, to prioritize likely causal mutations from genotype, gene expression, metabolite and phenotypes; and BIOMARK, to detect biomarkers for disease progression from longitudinal blood sample transcriptome and metabolome profiling.
Open-source software to implement causal stability ranking for high-dimensional genotype dataOpensource software that implements causal stability ranking for highdimensional genotype data
Open-source software for the standardized application of existing methods in liquid biopsy data analysisOpen-source software for the standardized application of existing methods in liquid biopsy data analysis, supported by online catalogue of existing methods and data resources.
Open-source software implementing InteractiveReports and catalogue of standard templates.Open-source software implementing InteractiveReports for displaying and scripting reproducible workflows; and a software catalogue of standard templates for informed decision-making.
Open-source software to estimate structured sparse models from multi-omics dataRelease of open-source software to estimate structured sparse models from multi-omics data.
Open-source software implementing end-to-end analysis and integrating the results from T1.1-1.5Open-source software implementing end-to-end analysis and integrating the results from T1.1-1.5, with documentation suitable for end-users.
Technical report on approaches to outlier detection in patient ’omics data
Technical report on biomarkers analysed with transcriptome and metabolome data and technical report on novel pathomechanisms
Technical report on biomarkers analysed in >=100 samples with transcriptome and metabolome data; and technical report on novel pathomechanism(s) leading to impaired energy metabolism discovered by multi-omic patient data analysis
Technical report on existing and novel methodsTechnical report on existing methods and novel methods developed in WP2
Technical report with best practice guidelines and software packageTechnical report with definitions and best practice guidelines; and software package for simulation of experimental design and choice of validation sites in cancer genomics.
Technical report with evaluation of performance improvement or regression from D9.2Technical report with evaluation of performance improvement or regression from D9.1
White paper description software design principles and open-source software implementation of SOUNDHub and SOUNDData.White paper describing software design principles and implementations; and open-source software implementation of SOUNDHub (annotation) amd SOUNDData (experiment data) services and clients, with specific development of controlled and federated data access.
Technical report describing the design of re-capture platform for deep sequencing and validationTechnical report describing the design of re-capture platform for deep sequencing and validation on independent patient cohort.
Technical report on new disease entities that were identified using novel statistical methodsTechnical report describing the data structure and methods for operating on screening data, as described in T1.1
Technical report describing the data structure and methods for operating on screening data as described in T11
Three or more SOUNDData public data resources as identified and developed in collaboration with WP leads; four or more SOUNDHub/AnnotationHub public data resources.
Website of InteractiveReports for select outcomes of WP2, 5-7.Make available InteractiveReports for select outcomes of WP2, 5-7 on website.
Pubblicazioni
Autori:
Ricard Argelaguet, Britta Velten, Damien Arnol, Sascha Dietrich, Thorsten Zenz, John C Marioni, Florian Buettner, Wolfgang Huber, Oliver Stegle
Pubblicato in:
Molecular Systems Biology, Numero 14/6, 2018, Pagina/e e8124, ISSN 1744-4292
Editore:
Nature Publishing Group
DOI:
10.15252/msb.20178124
Autori:
Sascha Dietrich, Małgorzata Oleś, Junyan Lu, Leopold Sellner, Simon Anders, Britta Velten, Bian Wu, Jennifer Hüllein, Michelle da Silva Liberio, Tatjana Walther, Lena Wagner, Sophie Rabe, Sonja Ghidelli-Disse, Marcus Bantscheff, Andrzej K. Oleś, Mikołaj Słabicki, Andreas Mock, Christopher C. Oakes, Shihui Wang, Sina Oppermann, Marina Lukas, Vladislav Kim, Martin Sill, Axel Benner, Anna Jauch
Pubblicato in:
Journal of Clinical Investigation, Numero 128/1, 2018, Pagina/e 427-445, ISSN 0021-9738
Editore:
American Society for Clinical Investigation
DOI:
10.1172/JCI93801
Autori:
Laura S. Kremer, Daniel M. Bader, Christian Mertes, Robert Kopajtich, Garwin Pichler, Arcangela Iuso, Tobias B. Haack, Elisabeth Graf, Thomas Schwarzmayr, Caterina Terrile, Eliška Koňaříková, Birgit Repp, Gabi Kastenmüller, Jerzy Adamski, Peter Lichtner, Christoph Leonhardt, Benoit Funalot, Alice Donati, Valeria Tiranti, Anne Lombes, Claude Jardel, Dieter Gläser, Robert W. Taylor, Daniele G
Pubblicato in:
Nature Communications, Numero 8, 2017, Pagina/e 15824, ISSN 2041-1723
Editore:
Nature Publishing Group
DOI:
10.1038/ncomms15824
Autori:
Georg Stricker, Mathilde Galinier, Julien Gagneur
Pubblicato in:
BMC Bioinformatics, Numero 19/1, 2018, ISSN 1471-2105
Editore:
BioMed Central
DOI:
10.1186/s12859-018-2238-7
Autori:
Vicente A. Yépez, Laura S. Kremer, Arcangela Iuso, Mirjana Gusic, Robert Kopajtich, Eliška Koňaříková, Agnieszka Nadel, Leonhard Wachutka, Holger Prokisch, Julien Gagneur
Pubblicato in:
PLOS ONE, Numero 13/7, 2018, Pagina/e e0199938, ISSN 1932-6203
Editore:
Public Library of Science
DOI:
10.1371/journal.pone.0199938
Autori:
Marta B. Lopes, André Veríssimo, Eunice Carrasquinha, Sandra Casimiro, Niko Beerenwinkel, Susana Vinga
Pubblicato in:
BMC Bioinformatics, Numero 19/1, 2018, ISSN 1471-2105
Editore:
BioMed Central
DOI:
10.1186/s12859-018-2149-7
Autori:
Eunice Carrasquinha, André Veríssimo, Marta B. Lopes, Susana Vinga
Pubblicato in:
BioData Mining, Numero 11/1, 2018, ISSN 1756-0381
Editore:
BioMed Central
DOI:
10.1186/s13040-018-0162-z
Autori:
Pieter Segaert, Marta B Lopes, Sandra Casimiro, Susana Vinga, Peter J Rousseeuw
Pubblicato in:
Statistical Methods in Medical Research, 2018, Pagina/e 096228021879472, ISSN 0962-2802
Editore:
SAGE Publications
DOI:
10.1177/0962280218794722
Autori:
Sarah Louise Stenton, Holger Prokisch
Pubblicato in:
Essays In Biochemistry, Numero 62/3, 2018, Pagina/e 399-408, ISSN 0071-1365
Editore:
Portland Press, Ltd.
DOI:
10.1042/EBC20170110
Autori:
Arcangela Iuso, Marit Wiersma, Hans-Joachim Schüller, Ben Pode-Shakked, Dina Marek-Yagel, Mathias Grigat, Thomas Schwarzmayr, Riccardo Berutti, Bader Alhaddad, Bart Kanon, Nicola A. Grzeschik, Jürgen G. Okun, Zeev Perles, Yishay Salem, Ortal Barel, Amir Vardi, Marina Rubinshtein, Tal Tirosh, Gal Dubnov-Raz, Ana C. Messias, Caterina Terrile, Iris Barshack, Alex Volkov, Camilla Avivi, Eran Eyal, E
Pubblicato in:
The American Journal of Human Genetics, Numero 102/6, 2018, Pagina/e 1018-1030, ISSN 0002-9297
Editore:
University of Chicago Press
DOI:
10.1016/j.ajhg.2018.03.022
Autori:
Miroslav P Milev, Claudio Graziano, Daniela Karall, Willemijn F E Kuper, Noraldin Al-Deri, Duccio Maria Cordelli, Tobias B Haack, Katharina Danhauser, Arcangela Iuso, Flavia Palombo, Tommaso Pippucci, Holger Prokisch, Djenann Saint-Dic, Marco Seri, Daniela Stanga, Giovanna Cenacchi, Koen L I van Gassen, Johannes Zschocke, Christine Fauth, Johannes A Mayr, Michael Sacher, Peter M van Hasselt
Pubblicato in:
Journal of Medical Genetics, 2018, Pagina/e jmedgenet-2018-105441, ISSN 0022-2593
Editore:
British Medical Association
DOI:
10.1136/jmedgenet-2018-105441
Autori:
Birgit M. Repp, Elisa Mastantuono, Charlotte L. Alston, Manuel Schiff, Tobias B. Haack, Agnes Rötig, Anna Ardissone, Anne Lombès, Claudia B. Catarino, Daria Diodato, Gudrun Schottmann, Joanna Poulton, Alberto Burlina, An Jonckheere, Arnold Munnich, Boris Rolinski, Daniele Ghezzi, Dariusz Rokicki, Diana Wellesley, Diego Martinelli, Ding Wenhong, Eleonora Lamantea, Elsebet Ostergaard, Ewa Pronicka
Pubblicato in:
Orphanet Journal of Rare Diseases, Numero 13/1, 2018, ISSN 1750-1172
Editore:
BioMed Central
DOI:
10.1186/s13023-018-0784-8
Autori:
René G. Feichtinger, Monika Oláhová, Yoshihito Kishita, Caterina Garone, Laura S. Kremer, Mikako Yagi, Takeshi Uchiumi, Alexis A. Jourdain, Kyle Thompson, Aaron R. D’Souza, Robert Kopajtich, Charlotte L. Alston, Johannes Koch, Wolfgang Sperl, Elisa Mastantuono, Tim M. Strom, Saskia B. Wortmann, Thomas Meitinger, Germaine Pierre, Patrick F. Chinnery, Zofia M. Chrzanowska-Lightowlers, Robert N.
Pubblicato in:
The American Journal of Human Genetics, Numero 101/4, 2017, Pagina/e 525-538, ISSN 0002-9297
Editore:
University of Chicago Press
DOI:
10.1016/j.ajhg.2017.08.015
Autori:
Laura S. Kremer, Saskia B. Wortmann, Holger Prokisch
Pubblicato in:
Journal of Inherited Metabolic Disease, Numero 41/3, 2018, Pagina/e 525-532, ISSN 0141-8955
Editore:
Kluwer Academic Publishers
DOI:
10.1007/s10545-017-0133-4
Autori:
Zhiwen Xu, Wing-Sze Lo, David B. Beck, Luise A. Schuch, Monika Oláhová, Robert Kopajtich, Yeeting E. Chong, Charlotte L. Alston, Elias Seidl, Liting Zhai, Ching-Fun Lau, Donna Timchak, Charles A. LeDuc, Alain C. Borczuk, Andrew F. Teich, Jane Juusola, Christina Sofeso, Christoph Müller, Germaine Pierre, Tom Hilliard, Peter D. Turnpenny, Matias Wagner, Matthias Kappler, Frank Brasch, John Paul B
Pubblicato in:
The American Journal of Human Genetics, Numero 103/1, 2018, Pagina/e 100-114, ISSN 0002-9297
Editore:
University of Chicago Press
DOI:
10.1016/j.ajhg.2018.06.006
Autori:
Ruth I. C. Glasgow, Kyle Thompson, Inês A. Barbosa, Langping He, Charlotte L. Alston, Charu Deshpande, Michael A. Simpson, Andrew A. M. Morris, Axel Neu, Ulrike Löbel, Julie Hall, Holger Prokisch, Tobias B. Haack, Maja Hempel, Robert McFarland, Robert W. Taylor
Pubblicato in:
neurogenetics, Numero 18/4, 2017, Pagina/e 227-235, ISSN 1364-6745
Editore:
Springer Verlag
DOI:
10.1007/s10048-017-0526-4
Autori:
Christos Dimitrakopoulos, Sravanth Kumar Hindupur, Luca Häfliger, Jonas Behr, Hesam Montazeri, Michael N Hall, Niko Beerenwinkel
Pubblicato in:
Bioinformatics, Numero 34/14, 2018, Pagina/e 2441-2448, ISSN 1367-4803
Editore:
Oxford University Press
DOI:
10.1093/bioinformatics/bty148
Autori:
André Veríssimo, Arlindo Limede Oliveira, Marie-France Sagot, Susana Vinga
Pubblicato in:
BMC Bioinformatics, Numero 17/S16, 2016, ISSN 1471-2105
Editore:
BioMed Central
DOI:
10.1186/s12859-016-1310-4
Autori:
Samira Ait-El-Mkadem, Manal Dayem-Quere, Mirjana Gusic, Annabelle Chaussenot, Sylvie Bannwarth, Bérengère François, Emmanuelle C. Genin, Konstantina Fragaki, Catharina L.M. Volker-Touw, Christelle Vasnier, Valérie Serre, Koen L.I. van Gassen, Françoise Lespinasse, Susan Richter, Graeme Eisenhofer, Cécile Rouzier, Fanny Mochel, Anne De Saint-Martin, Marie-Thérèse Abi Warde, Monique G.M. de
Pubblicato in:
The American Journal of Human Genetics, Numero 100/1, 2017, Pagina/e 151-159, ISSN 0002-9297
Editore:
University of Chicago Press
DOI:
10.1016/j.ajhg.2016.11.014
Autori:
Ariane L. Hofmann, Jonas Behr, Jochen Singer, Jack Kuipers, Christian Beisel, Peter Schraml, Holger Moch, Niko Beerenwinkel
Pubblicato in:
BMC Bioinformatics, Numero 18/1, 2017, ISSN 1471-2105
Editore:
BioMed Central
DOI:
10.1186/s12859-016-1417-7
Autori:
Robert Kopajtich, Kei Murayama, Andreas R. Janecke, Tobias B. Haack, Maximilian Breuer, A.S. Knisely, Inga Harting, Toya Ohashi, Yasushi Okazaki, Daisaku Watanabe, Yoshimi Tokuzawa, Urania Kotzaeridou, Stefan Kölker, Sven Sauer, Matthias Carl, Simon Straub, Andreas Entenmann, Elke Gizewski, René G. Feichtinger, Johannes A. Mayr, Karoline Lackner, Tim M. Strom, Thomas Meitinger, Thomas Müll
Pubblicato in:
The American Journal of Human Genetics, Numero 99/2, 2016, Pagina/e 414-422, ISSN 0002-9297
Editore:
University of Chicago Press
DOI:
10.1016/j.ajhg.2016.05.027
Autori:
Georg Stricker, Alexander Engelhardt, Daniel Schulz, Matthias Schmid, Achim Tresch, Julien Gagneur
Pubblicato in:
Bioinformatics, 2017, ISSN 1367-4803
Editore:
Oxford University Press
DOI:
10.1093/bioinformatics/btx150
Autori:
Elson Tomás, Susana Vinga, Alexandra M. Carvalho
Pubblicato in:
Computational Statistics, 2017, ISSN 0943-4062
Editore:
Physica-Verlag Gmbh und Co.
DOI:
10.1007/s00180-016-0707-x
Autori:
Lindsey Van Haute, Sabine Dietmann, Laura Kremer, Shobbir Hussain, Sarah F. Pearce, Christopher A. Powell, Joanna Rorbach, Rebecca Lantaff, Sandra Blanco, Sascha Sauer, Urania Kotzaeridou, Georg F. Hoffmann, Yasin Memari, Anja Kolb-Kokocinski, Richard Durbin, Johannes A. Mayr, Michaela Frye, Holger Prokisch, Michal Minczuk
Pubblicato in:
Nature Communications, Numero 7, 2016, Pagina/e 12039, ISSN 2041-1723
Editore:
Nature Publishing Group
DOI:
10.1038/ncomms12039
Autori:
Thomas Thurnherr, Franziska Singer, Daniel J. Stekhoven, Niko Beerenwinkel
Pubblicato in:
F1000Research, Numero 5, 2016, Pagina/e 1963, ISSN 2046-1402
Editore:
F1000 Research Ltd.
DOI:
10.12688/f1000research.9357.2
Autori:
Felix Brechtmann, Agne Matuseviciute, Christian Mertes, Vicente A Yepez, Ziga Avsec, Maximilian Herzog, Daniel Magnus Bader, Holger Prokisch, Julien Gagneur
Pubblicato in:
bioRxiv, 2018
Editore:
bioRxiv
DOI:
10.1101/322149
Autori:
Dongxue Wang, Basak Eraslan, Thomas Wieland, Bjorn M Hallstrom, Thomas Hopf, Daniel Paul Zolg, Jana Zecha, Anna Asplund, Li-hua Li, Chen Meng, Martin Frejno, Tobias Schmidt, Karsten Schnatbaum, Mathias Wilhelm, Fredrik Ponten, Mathias Uhlen, Julien Gagneur, Hannes Hahne, Bernhard Kuster
Pubblicato in:
bioRxiv, 2018
Editore:
bioRxiv
DOI:
10.1101/357137
Autori:
Basak Eraslan, Dongxue Wang, Mirjana Gusic, Holger Prokisch, Bjorn M Hallstrom, Mathias Uhlen, Anna Asplund, Fredrik Ponten, Thomas Wieland, Thomas Hopf, Hannes Hahne, Bernhard Kuster, Julien Gagneur
Pubblicato in:
bioRxiv, 2018
Editore:
bioRxiv
DOI:
10.1101/353763
Autori:
André Veríssimo, Eunice Carrasquinha, Marta B. Lopes, Arlindo L. Oliveira, Marie-France Sagot, Susana Vinga
Pubblicato in:
2018
Editore:
bioRxiv
Autori:
Eunice Carrasquinha, André Veríssimo, Susana Vinga
Pubblicato in:
2018
Editore:
bioRxiv
DOI:
10.1101/421917
Autori:
Laura S Kremer, View ORCID ProfileDaniel M Bader, Christian Mertes, Robert Kopajtich, Garwin Pichler, Arcangela Iuso, Tobias B Haack, Elisabeth Graf, Thomas Schwarzmayr, Caterina Terrile, Eliska Konafikova, Birgit Repp, Gabi Kastenmüller, Jerzy Adamski, Peter Lichtner, Christoph Leonhardt, Benoit Funalot, Alice Donati, Valeria Tiranti, Anne Lombes, Claude Jardel, Dieter Gläser, Robert W Taylor,
Pubblicato in:
2016
Editore:
bioRxiv
DOI:
10.1101/066738
Autori:
Solaimani P., Kallen M., Bertram A.
Pubblicato in:
F1000Research, 2016
Editore:
F1000Research
DOI:
10.7490/f1000research.1113288.1
È in corso la ricerca di dati su OpenAIRE...
Si è verificato un errore durante la ricerca dei dati su OpenAIRE
Nessun risultato disponibile