Morris A. Swertz
Orcid: 0000-0002-0979-3401
According to our database1,
Morris A. Swertz
authored at least 50 papers
between 2004 and 2024.
Collaborative distances:
Collaborative distances:
Timeline
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Bibliography
2024
J. Biomed. Semant., December, 2024
Database J. Biol. Databases Curation, January, 2024
Genom. Proteom. Bioinform., 2024
Proceedings of the 15th International Conference on Semantic Web Applications and Tools for Health Care and Life Sciences, 2024
Comparing Sequence-Based and Literature-Based Pathogenicity Scoring Methods for Human Variants.
Proceedings of the Digital Health and Informatics Innovations for Sustainable Health Care Systems, 2024
2023
A Resource for Guiding Data Stewards to Make European Rare Disease Patient Registries FAIR.
Data Sci. J., January, 2023
Semi-automatic translation of medicine usage data (in Dutch, free-text) from Lifelines COVID-19 questionnaires to ATC codes.
Database J. Biol. Databases Curation, 2023
Visualisation and Exploration of Linked Data Using Virtual Reality - a preview of Graph2VR.
Proceedings of the 14th International Conference on Semantic Web Applications and Tools for Health Care and Life Sciences (SWAT4HCLS 2023), 2023
Surveyed common data access policies preferences amongst European Reference Networks.
Proceedings of the 14th International Conference on Semantic Web Applications and Tools for Health Care and Life Sciences (SWAT4HCLS 2023), 2023
2022
Semantic modelling of common data elements for rare disease registries, and a prototype workflow for their deployment over registry data.
J. Biomed. Semant., 2022
2020
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.
F1000Research, 2020
BMC Bioinform., 2020
2019
Bioinform., 2019
Proceedings of the 12th International Conference on Semantic Web Applications and Tools for Health Care and Life Sciences, 2019
2018
NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing.
BMC Bioinform., 2018
Machine Learning for Multi-Omics Data Integration and Variant Pathogenicity Estimation.
Proceedings of the 14th IEEE International Conference on e-Science, 2018
2017
PeerJ Prepr., 2017
BiobankUniverse: automatic matchmaking between datasets for biobank data discovery and integration.
Bioinform., 2017
2016
PeerJ Prepr., 2016
MOLGENIS/connect: a system for semi-automatic integration of heterogeneous phenotype data with applications in biobanks.
Bioinform., 2016
Proceedings of the Astroinformatics 2016, Sorrento, Italy, October 19-25, 2016, 2016
2015
Proceedings of the Smart Health - Open Problems and Future Challenges, 2015
PyPedia: using the wiki paradigm as crowd sourcing environment for bioinformatics protocols.
Source Code Biol. Medicine, 2015
BiobankConnect: software to rapidly connect data elements for pooled analysis across biobanks using ontological and lexical indexing.
J. Am. Medical Informatics Assoc., 2015
SORTA: a system for ontology-based re-coding and technical annotation of biomedical phenotype data.
Database J. Biol. Databases Curation, 2015
2014
WormQTL<sup>HD</sup> - a web database for linking human disease to natural variation data in <i>C. elegans</i>.
Nucleic Acids Res., 2014
Proceedings of the Machine Learning and Knowledge Discovery in Databases, 2014
2013
WormQTL - public archive and analysis web portal for natural variation data in <i>Caenorhabditis</i> spp.
Nucleic Acids Res., 2013
Proceedings of the 5th International Workshop on Science Gateways, 2013
Visualization of Bioinformatics Workflows for Ease of Understanding and Design Activities.
Proceedings of the BIOINFORMATICS 2013 - Proceedings of the International Conference on Bioinformatics Models, Methods and Algorithms, Barcelona, Spain, 11, 2013
2012
BMC Bioinform., 2012
Bioinform., 2012
Bioinformatics tools and database resources for systems genetics analysis in mice - a short review and an evaluation of future needs.
Briefings Bioinform., 2012
Introducing Data Provenance and Error Handling for NGS Workflows within the MOLGENIS Computational Framework.
Proceedings of the BIOINFORMATICS 2012 - Proceedings of the International Conference on Bioinformatics Models, Methods and Algorithms, Vilamoura, Algarve, Portugal, 1, 2012
2011
BMC Bioinform., 2011
A high-throughput processing service for retention time alignment of complex proteomics and metabolomics LC-MS data.
Bioinform., 2011
Proceedings of the 19th International Euromicro Conference on Parallel, 2011
2010
BMC Bioinform., 2010
Database J. Biol. Databases Curation, 2010
Finding and sharing: new approaches to registries of databases and services for the biomedical sciences.
Database J. Biol. Databases Curation, 2010
2009
designGG: an R-package and web tool for the optimal design of genetical genomics experiments.
BMC Bioinform., 2009
2008
Solutions for data integration in functional genomics: a critical assessment and case study.
Briefings Bioinform., 2008
Proceedings of the 8th IEEE International Conference on Bioinformatics and Bioengineering, 2008
2005
2004
Molecular Genetics Information System (MOLGENIS): alternatives in developing local experimental genomics databases.
Bioinform., 2004