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Bioinformatics (Oxford, England)|August 1, 2014
Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseasesDamian Smedley, Sebastian Köhler, Johanna Christina Czeschik, et al.Database : the Journal of Biological Databases and Curation|March 1, 2015
Automatic concept recognition using the human phenotype ontology reference and test suite corporaTudor Groza, Sebastian Köhler, Sandra Doelken, et al.American Journal of Human Genetics|October 6, 2009
Clinical diagnostics in human genetics with semantic similarity searches in ontologiesSebastian Köhler, Marcel H Schulz, Peter Krawitz, et al.Genome Medicine|December 5, 2014
Genomic data sharing for translational research and diagnosticsPeter N RobinsonGenome Biology|December 22, 2010
Whole-exome sequencing for finding de novo mutations in sporadic mental retardationPeter N RobinsonJournal of Alzheimer'S Disease : JAD|December 18, 2020
Primary Prevention of Dementia: An Ethical ReviewDorothee Horstkötter, Kay Deckers, Sebastian KöhlerJournal of Medical Genetics|October 5, 2014
Clinical interpretation of CNVs with cross-species phenotype dataSebastian Köhler, Uwe Schoeneberg, Johanna Christina Czeschik, et al.BMC Bioinformatics|February 14, 2006
HotSwap for bioinformatics: a STRAP tutorialChristoph Gille, Peter N RobinsonPageof 58