Dominik Seelow

According to our database, Dominik Seelow authored at least 14 papers between 2004 and 2023.

Collaborative distances:

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

2023

Editorial: the 21st annual <i>Nucleic Acids Research</i> Web Server Issue 2023.

Dominik Seelow

Nucleic Acids Res., July, 2023

2022

FABIAN-variant: predicting the effects of DNA variants on transcription factor binding.

Robin Steinhaus, Peter N. Robinson, Dominik Seelow

Nucleic Acids Res., 2022

Deep phenotyping: symptom annotation made simple with SAMS.

Robin Steinhaus, Sebastian Proft, Evelyn Seelow, Tobias Schalau, Peter N. Robinson, Dominik Seelow

Nucleic Acids Res., 2022

AutozygosityMapper: Identification of disease-mutations in consanguineous families.

Robin Steinhaus, Felix Boschann, Melanie Vogel, Björn Fischer-Zirnsak, Dominik Seelow

Nucleic Acids Res., 2022

RegEl corpus: identifying DNA regulatory elements in the scientific literature.

Samuele Garda, Freyda Lenihan-Geels, Sebastian Proft, Stefanie Hochmuth, Markus Schuelke, Dominik Seelow, Ulf Leser

Database J. Biol. Databases Curation, 2022

2021

MutationTaster2021.

Robin Steinhaus, Sebastian Proft, Markus Schuelke, David N. Cooper, Jana Marie Schwarz, Dominik Seelow

Nucleic Acids Res., 2021

Aviator: a web service for monitoring the availability of web services.

Tobias Fehlmann, Fabian Kern, Pascal Hirsch, Robin Steinhaus, Dominik Seelow, Andreas Keller

Nucleic Acids Res., 2021

2020

VarFish: comprehensive DNA variant analysis for diagnostics and research.

Manuel Holtgrewe, Oliver Stolpe, Mikko Nieminen, Stefan Mundlos, Alexej Knaus, Uwe Kornak, Dominik Seelow, Lara Segebrecht, Malte Spielmann, Björn Fischer-Zirnsak, Felix Boschann, Ute Scholl, Nadja Ehmke, Dieter Beule

Nucleic Acids Res., 2020

2019

RegulationSpotter: annotation and interpretation of extratranscriptic DNA variants.

Jana Marie Schwarz, Daniela Hombach, Sebastian Köhler, David N. Cooper, Markus Schuelke, Dominik Seelow

Nucleic Acids Res., 2019

MutationDistiller: user-driven identification of pathogenic DNA variants.

Daniela Hombach, Markus Schuelke, Ellen Knierim, Nadja Ehmke, Jana Marie Schwarz, Björn Fischer-Zirnsak, Dominik Seelow

Nucleic Acids Res., 2019

2012

HomozygosityMapper2012 - bridging the gap between homozygosity mapping and deep sequencing.

Dominik Seelow, Markus Schuelke

Nucleic Acids Res., 2012

2009

HomozygosityMapper - an interactive approach to homozygosity mapping.

Dominik Seelow, Markus Schuelke, Friedhelm Hildebrandt, Peter Nürnberg

Nucleic Acids Res., 2009

2007

AssociationDB: web-based exploration of genomic association.

Dominik Seelow, Katrin Hoffmann, Tom H. Lindner

Bioinform., 2007

2004

d-matrix - database exploration, visualization and analysis.

Dominik Seelow, Raffaello Galli, Siegrun Mebus, Hans-Peter Sperling, Hans Lehrach, Silke Sperling

BMC Bioinform., 2004