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Dominik Seelow

Showing results (11-20 of 62) with videos related to

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Journal of Medical Genetics|June 5, 2013
CNVinspector: a web-based tool for the interactive evaluation of copy number variations in single patients and in cohortsEllen Knierim, Jana Marie Schwarz, Markus Schuelke, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Novel sequencing technologies and bioinformatic tools for deciphering the non-coding genomeJana Marie Schwarz, Richard Lüpken, Dominik Seelow, et al.
Nucleic Acids Research|April 28, 2020
Pervasive and CpG-dependent promoter-like characteristics of transcribed enhancersRobin Steinhaus, Tonatiuh Gonzalez, Dominik Seelow, et al.
BMC Genomics|July 25, 2014
GrabBlur--a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF filesBjörn Stade, Dominik Seelow, Ingo Thomsen, et al.
Plos One|December 6, 2011
Systematic comparison of three methods for fragmentation of long-range PCR products for next generation sequencingEllen Knierim, Barbara Lucke, Jana Marie Schwarz, et al.
Mitochondrion|December 3, 2014
Clinical application of whole exome sequencing reveals a novel compound heterozygous TK2-mutation in two brothers with rapidly progressive combined muscle-brain atrophy, axonal neuropathy, and status epilepticusEllen Knierim, Dominik Seelow, Esther Gill, et al.
Nucleic Acids Research|April 30, 2022
AutozygosityMapper: Identification of disease-mutations in consanguineous familiesRobin Steinhaus, Felix Boschann, Melanie Vogel, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Public data sources for regulatory genomic featuresSamuele Garda, Jana Marie Schwarz, Markus Schuelke, et al.
Human Genetics|October 18, 2002
Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneityGerald Stöber, Dominik Seelow, Franz Rüschendorf, et al.
BMC Genomics|May 23, 2016
A systematic, large-scale comparison of transcription factor binding site modelsDaniela Hombach, Jana Marie Schwarz, Peter N Robinson, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|June 5, 2013
CNVinspector: a web-based tool for the interactive evaluation of copy number variations in single patients and in cohortsEllen Knierim, Jana Marie Schwarz, Markus Schuelke, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Novel sequencing technologies and bioinformatic tools for deciphering the non-coding genomeJana Marie Schwarz, Richard Lüpken, Dominik Seelow, et al.
Nucleic Acids Research|April 28, 2020
Pervasive and CpG-dependent promoter-like characteristics of transcribed enhancersRobin Steinhaus, Tonatiuh Gonzalez, Dominik Seelow, et al.
BMC Genomics|July 25, 2014
GrabBlur--a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF filesBjörn Stade, Dominik Seelow, Ingo Thomsen, et al.
Plos One|December 6, 2011
Systematic comparison of three methods for fragmentation of long-range PCR products for next generation sequencingEllen Knierim, Barbara Lucke, Jana Marie Schwarz, et al.
Mitochondrion|December 3, 2014
Clinical application of whole exome sequencing reveals a novel compound heterozygous TK2-mutation in two brothers with rapidly progressive combined muscle-brain atrophy, axonal neuropathy, and status epilepticusEllen Knierim, Dominik Seelow, Esther Gill, et al.
Nucleic Acids Research|April 30, 2022
AutozygosityMapper: Identification of disease-mutations in consanguineous familiesRobin Steinhaus, Felix Boschann, Melanie Vogel, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Public data sources for regulatory genomic featuresSamuele Garda, Jana Marie Schwarz, Markus Schuelke, et al.
Human Genetics|October 18, 2002
Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneityGerald Stöber, Dominik Seelow, Franz Rüschendorf, et al.
BMC Genomics|May 23, 2016
A systematic, large-scale comparison of transcription factor binding site modelsDaniela Hombach, Jana Marie Schwarz, Peter N Robinson, et al.
Pageof 7