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2020 – today
- 2023
[j4]Sven Berres, Jörg Gromoll, Marius Wöste, Sarah Sandmann
, Sandra Laurentino:
OGRE: calculate, visualize, and analyze overlap between genomic input regions and public annotations. BMC Bioinform. 24(1): 300 (2023)
2010 – 2019
- 2018
- [j3]Sarah Sandmann, Mohsen Karimi, Aniek O. de Graaf, Christian Rohde, Stefanie Göllner, Julian Varghese, Jan Ernsting, Gunilla Walldin, Bert A. van der Reijden, Carsten Müller-Tidow, Luca Malcovati, Eva Hellström-Lindberg, Joop H. Jansen, Martin Dugas:
appreci8: a pipeline for precise variant calling integrating 8 tools. Bioinform. 34(24): 4205-4212 (2018) - [j2]Julian Varghese, Maren Kleine, Sophia Isabella Gessner, Sarah Sandmann, Martin Dugas:
Effects of computerized decision support system implementations on patient outcomes in inpatient care: a systematic review. J. Am. Medical Informatics Assoc. 25(5): 593-602 (2018) - 2017
- [b1]Sarah Sandmann:
Evaluating variant calling tools for non-matched next-generation sequencing data. University of Münster, Germany, 2017 - [j1]Sarah Sandmann, Aniek O. de Graaf, Martin Dugas:
BBCAnalyzer: a visual approach to facilitate variant calling. BMC Bioinform. 18(1): 133:1-133:6 (2017) - [c1]Julian Varghese, Maren Kleine, Sophia Isabella Gessner, Sarah Sandmann, Martin Dugas:
Medical Effect of Venous Thromboembolism Prophylaxis Systems and Common Input Categories: Preliminary Findings from a Systematic Review. MedInfo 2017: 1175-1179
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