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David Ellinghaus

Showing results (11-20 of 133) with videos related to

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Bioinformatics (Oxford, England)|October 20, 2022
MAGScoT: a fast, lightweight and accurate bin-refinement toolMalte Christoph Rühlemann, Eike Matthias Wacker, David Ellinghaus, et al.
Bioinformatics (Oxford, England)|May 7, 2016
Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility lociAndré Lacour, David Ellinghaus, Stefan Schreiber, et al.
Inflammatory Bowel Diseases|September 7, 2016
A Promoter Variant Within the Aryl Hydrocarbon Receptor Gene Is Associated with an Epithelial Barrier Defect in Smokers with Crohn's DiseaseMatthias Prager, Janine Büttner, Philip Grunert, et al.
Human Genetics|December 18, 2008
A comprehensive evaluation of SNP genotype imputationMichael Nothnagel, David Ellinghaus, Stefan Schreiber, et al.
Nature Communications|June 11, 2026
TOFU-MAaPO: fast, scalable and reproducible analysis of large metagenome sequence data from the Sequence Read ArchiveEike Matthias Wacker, Malte Christoph Rühlemann, Andre Franke, et al.
European Journal of Human Genetics : EJHG|February 2, 2012
1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 DataJie Huang, David Ellinghaus, Andre Franke, et al.
Gut|October 9, 2023
Mendelian randomisation shows diverticular disease and irritable bowel syndrome increase the risk of haemorrhoidal diseaseSimonas Juzenas, David Ellinghaus, Serena Sanna, et al.
Scientific Reports|March 30, 2020
A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samplesFlorian Uellendahl-Werth, Markus Wolfien, Andre Franke, et al.
BMC Genetics|February 15, 2017
Opportunities and challenges of whole-genome and -exome sequencingBritt-Sabina Petersen, Broder Fredrich, Marc P Hoeppner, et al.
Source Code for Biology and Medicine|March 28, 2017
LitDB - Keeping Track of Research Papers From Your Institute Made SimpleJörn Bethune, Lars Kraemer, Ingo Thomsen, et al.
Pageof 14

Showing results (11-20 of 133) with videos related to

Sort By:
Pageof 14
Bioinformatics (Oxford, England)|October 20, 2022
MAGScoT: a fast, lightweight and accurate bin-refinement toolMalte Christoph Rühlemann, Eike Matthias Wacker, David Ellinghaus, et al.
Bioinformatics (Oxford, England)|May 7, 2016
Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility lociAndré Lacour, David Ellinghaus, Stefan Schreiber, et al.
Inflammatory Bowel Diseases|September 7, 2016
A Promoter Variant Within the Aryl Hydrocarbon Receptor Gene Is Associated with an Epithelial Barrier Defect in Smokers with Crohn's DiseaseMatthias Prager, Janine Büttner, Philip Grunert, et al.
Human Genetics|December 18, 2008
A comprehensive evaluation of SNP genotype imputationMichael Nothnagel, David Ellinghaus, Stefan Schreiber, et al.
Nature Communications|June 11, 2026
TOFU-MAaPO: fast, scalable and reproducible analysis of large metagenome sequence data from the Sequence Read ArchiveEike Matthias Wacker, Malte Christoph Rühlemann, Andre Franke, et al.
European Journal of Human Genetics : EJHG|February 2, 2012
1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 DataJie Huang, David Ellinghaus, Andre Franke, et al.
Gut|October 9, 2023
Mendelian randomisation shows diverticular disease and irritable bowel syndrome increase the risk of haemorrhoidal diseaseSimonas Juzenas, David Ellinghaus, Serena Sanna, et al.
Scientific Reports|March 30, 2020
A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samplesFlorian Uellendahl-Werth, Markus Wolfien, Andre Franke, et al.
BMC Genetics|February 15, 2017
Opportunities and challenges of whole-genome and -exome sequencingBritt-Sabina Petersen, Broder Fredrich, Marc P Hoeppner, et al.
Source Code for Biology and Medicine|March 28, 2017
LitDB - Keeping Track of Research Papers From Your Institute Made SimpleJörn Bethune, Lars Kraemer, Ingo Thomsen, et al.
Pageof 14