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Dominik Seelow

Showing results (21-30 of 62) with videos related to

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Nucleic Acids Research|May 26, 2021
Aviator: a web service for monitoring the availability of web servicesTobias Fehlmann, Fabian Kern, Pascal Hirsch, et al.
BMC Bioinformatics|October 30, 2004
d-matrix - database exploration, visualization and analysisDominik Seelow, Raffaello Galli, Siegrun Mebus, et al.
American Journal of Human Genetics|October 28, 2008
The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary diseasePeter N Robinson, Sebastian Köhler, Sebastian Bauer, et al.
Nucleic Acids Research|May 7, 2022
Deep phenotyping: symptom annotation made simple with SAMSRobin Steinhaus, Sebastian Proft, Evelyn Seelow, et al.
Clinical Genetics|November 13, 2018
Phenotero: Annotate as you writeDaniela Hombach, Jana M Schwarz, Ellen Knierim, et al.
BMC Genomics|December 4, 2023
Discovery of a non-canonical GRHL1 binding site using deep convolutional and recurrent neural networksSebastian Proft, Janna Leiz, Udo Heinemann, et al.
Nucleic Acids Research|April 24, 2021
MutationTaster2021Robin Steinhaus, Sebastian Proft, Markus Schuelke, et al.
Nucleic Acids Research|May 21, 2019
RegulationSpotter: annotation and interpretation of extratranscriptic DNA variantsJana Marie Schwarz, Daniela Hombach, Sebastian Köhler, et al.
Database : the Journal of Biological Databases and Curation|June 27, 2022
RegEl corpus: identifying DNA regulatory elements in the scientific literatureSamuele Garda, Freyda Lenihan-Geels, Sebastian Proft, et al.
Nucleic Acids Research|May 21, 2019
MutationDistiller: user-driven identification of pathogenic DNA variantsDaniela Hombach, Markus Schuelke, Ellen Knierim, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
Nucleic Acids Research|May 26, 2021
Aviator: a web service for monitoring the availability of web servicesTobias Fehlmann, Fabian Kern, Pascal Hirsch, et al.
BMC Bioinformatics|October 30, 2004
d-matrix - database exploration, visualization and analysisDominik Seelow, Raffaello Galli, Siegrun Mebus, et al.
American Journal of Human Genetics|October 28, 2008
The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary diseasePeter N Robinson, Sebastian Köhler, Sebastian Bauer, et al.
Nucleic Acids Research|May 7, 2022
Deep phenotyping: symptom annotation made simple with SAMSRobin Steinhaus, Sebastian Proft, Evelyn Seelow, et al.
Clinical Genetics|November 13, 2018
Phenotero: Annotate as you writeDaniela Hombach, Jana M Schwarz, Ellen Knierim, et al.
BMC Genomics|December 4, 2023
Discovery of a non-canonical GRHL1 binding site using deep convolutional and recurrent neural networksSebastian Proft, Janna Leiz, Udo Heinemann, et al.
Nucleic Acids Research|April 24, 2021
MutationTaster2021Robin Steinhaus, Sebastian Proft, Markus Schuelke, et al.
Nucleic Acids Research|May 21, 2019
RegulationSpotter: annotation and interpretation of extratranscriptic DNA variantsJana Marie Schwarz, Daniela Hombach, Sebastian Köhler, et al.
Database : the Journal of Biological Databases and Curation|June 27, 2022
RegEl corpus: identifying DNA regulatory elements in the scientific literatureSamuele Garda, Freyda Lenihan-Geels, Sebastian Proft, et al.
Nucleic Acids Research|May 21, 2019
MutationDistiller: user-driven identification of pathogenic DNA variantsDaniela Hombach, Markus Schuelke, Ellen Knierim, et al.
Pageof 7