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Manuel Holtgrewe

Showing results (1-10 of 48) with videos related to

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Bioinformatics (Oxford, England)|August 28, 2012
RazerS 3: faster, fully sensitive read mappingDavid Weese, Manuel Holtgrewe, Knut Reinert
Bioinformatics (Oxford, England)|February 5, 2015
Methods for the detection and assembly of novel sequence in high-throughput sequencing dataManuel Holtgrewe, Leon Kuchenbecker, Knut Reinert
Bioinformatics (Oxford, England)|March 24, 2017
HLA-MA: simple yet powerful matching of samples using HLA typing resultsClemens Messerschmidt, Manuel Holtgrewe, Dieter Beule
BMC Bioinformatics|April 10, 2014
Genome alignment with graph data structures: a comparisonBirte Kehr, Kathrin Trappe, Manuel Holtgrewe, et al.
BMC Bioinformatics|May 28, 2011
A novel and well-defined benchmarking method for second generation read mappingManuel Holtgrewe, Anne-Katrin Emde, David Weese, et al.
Peerj|March 3, 2020
SCelVis: exploratory single cell data analysis on the desktop and in the cloudBenedikt Obermayer, Manuel Holtgrewe, Mikko Nieminen, et al.
Gigascience|July 27, 2023
SODAR: managing multiomics study data and metadataMikko Nieminen, Oliver Stolpe, Mathias Kuhring, et al.
BMC Medical Genomics|November 29, 2019
Identification and ranking of recurrent neo-epitopes in cancerEric Blanc, Manuel Holtgrewe, Arunraj Dhamodaran, et al.
Bioinformatics (Oxford, England)|August 28, 2014
Fiona: a parallel and automatic strategy for read error correctionMarcel H Schulz, David Weese, Manuel Holtgrewe, et al.
Bioinformatics (Oxford, England)|June 25, 2022
ClearCNV: CNV calling from NGS panel data in the presence of ambiguity and noiseVinzenz May, Leonard Koch, Björn Fischer-Zirnsak, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Bioinformatics (Oxford, England)|August 28, 2012
RazerS 3: faster, fully sensitive read mappingDavid Weese, Manuel Holtgrewe, Knut Reinert
Bioinformatics (Oxford, England)|February 5, 2015
Methods for the detection and assembly of novel sequence in high-throughput sequencing dataManuel Holtgrewe, Leon Kuchenbecker, Knut Reinert
Bioinformatics (Oxford, England)|March 24, 2017
HLA-MA: simple yet powerful matching of samples using HLA typing resultsClemens Messerschmidt, Manuel Holtgrewe, Dieter Beule
BMC Bioinformatics|April 10, 2014
Genome alignment with graph data structures: a comparisonBirte Kehr, Kathrin Trappe, Manuel Holtgrewe, et al.
BMC Bioinformatics|May 28, 2011
A novel and well-defined benchmarking method for second generation read mappingManuel Holtgrewe, Anne-Katrin Emde, David Weese, et al.
Peerj|March 3, 2020
SCelVis: exploratory single cell data analysis on the desktop and in the cloudBenedikt Obermayer, Manuel Holtgrewe, Mikko Nieminen, et al.
Gigascience|July 27, 2023
SODAR: managing multiomics study data and metadataMikko Nieminen, Oliver Stolpe, Mathias Kuhring, et al.
BMC Medical Genomics|November 29, 2019
Identification and ranking of recurrent neo-epitopes in cancerEric Blanc, Manuel Holtgrewe, Arunraj Dhamodaran, et al.
Bioinformatics (Oxford, England)|August 28, 2014
Fiona: a parallel and automatic strategy for read error correctionMarcel H Schulz, David Weese, Manuel Holtgrewe, et al.
Bioinformatics (Oxford, England)|June 25, 2022
ClearCNV: CNV calling from NGS panel data in the presence of ambiguity and noiseVinzenz May, Leonard Koch, Björn Fischer-Zirnsak, et al.
Pageof 5