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Bioinformatics (Oxford, England)
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August 28, 2012
RazerS 3: faster, fully sensitive read mapping
David Weese, Manuel Holtgrewe, Knut Reinert
Bioinformatics (Oxford, England)
|
February 5, 2015
Methods for the detection and assembly of novel sequence in high-throughput sequencing data
Manuel Holtgrewe, Leon Kuchenbecker, Knut Reinert
Bioinformatics (Oxford, England)
|
March 24, 2017
HLA-MA: simple yet powerful matching of samples using HLA typing results
Clemens Messerschmidt, Manuel Holtgrewe, Dieter Beule
BMC Bioinformatics
|
April 10, 2014
Genome alignment with graph data structures: a comparison
Birte Kehr, Kathrin Trappe, Manuel Holtgrewe, et al.
BMC Bioinformatics
|
May 28, 2011
A novel and well-defined benchmarking method for second generation read mapping
Manuel Holtgrewe, Anne-Katrin Emde, David Weese, et al.
Peerj
|
March 3, 2020
SCelVis: exploratory single cell data analysis on the desktop and in the cloud
Benedikt Obermayer, Manuel Holtgrewe, Mikko Nieminen, et al.
Gigascience
|
July 27, 2023
SODAR: managing multiomics study data and metadata
Mikko Nieminen, Oliver Stolpe, Mathias Kuhring, et al.
BMC Medical Genomics
|
November 29, 2019
Identification and ranking of recurrent neo-epitopes in cancer
Eric Blanc, Manuel Holtgrewe, Arunraj Dhamodaran, et al.
Bioinformatics (Oxford, England)
|
August 28, 2014
Fiona: a parallel and automatic strategy for read error correction
Marcel 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 noise
Vinzenz May, Leonard Koch, Björn Fischer-Zirnsak, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 48) with videos related to
Sort By:
Page
of 5
Bioinformatics (Oxford, England)
|
August 28, 2012
RazerS 3: faster, fully sensitive read mapping
David Weese, Manuel Holtgrewe, Knut Reinert
Bioinformatics (Oxford, England)
|
February 5, 2015
Methods for the detection and assembly of novel sequence in high-throughput sequencing data
Manuel Holtgrewe, Leon Kuchenbecker, Knut Reinert
Bioinformatics (Oxford, England)
|
March 24, 2017
HLA-MA: simple yet powerful matching of samples using HLA typing results
Clemens Messerschmidt, Manuel Holtgrewe, Dieter Beule
BMC Bioinformatics
|
April 10, 2014
Genome alignment with graph data structures: a comparison
Birte Kehr, Kathrin Trappe, Manuel Holtgrewe, et al.
BMC Bioinformatics
|
May 28, 2011
A novel and well-defined benchmarking method for second generation read mapping
Manuel Holtgrewe, Anne-Katrin Emde, David Weese, et al.
Peerj
|
March 3, 2020
SCelVis: exploratory single cell data analysis on the desktop and in the cloud
Benedikt Obermayer, Manuel Holtgrewe, Mikko Nieminen, et al.
Gigascience
|
July 27, 2023
SODAR: managing multiomics study data and metadata
Mikko Nieminen, Oliver Stolpe, Mathias Kuhring, et al.
BMC Medical Genomics
|
November 29, 2019
Identification and ranking of recurrent neo-epitopes in cancer
Eric Blanc, Manuel Holtgrewe, Arunraj Dhamodaran, et al.
Bioinformatics (Oxford, England)
|
August 28, 2014
Fiona: a parallel and automatic strategy for read error correction
Marcel 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 noise
Vinzenz May, Leonard Koch, Björn Fischer-Zirnsak, et al.
Page
of 5