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Anne-Katrin Emde

Showing results (1-10 of 38) with videos related to

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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.
Bioinformatics (Oxford, England)|July 17, 2014
Gustaf: Detecting and correctly classifying SVs in the NGS twilight zoneKathrin Trappe, Anne-Katrin Emde, Hans-Christian Ehrlich, et al.
Genome Research|July 14, 2009
RazerS--fast read mapping with sensitivity controlDavid Weese, Anne-Katrin Emde, Tobias Rausch, et al.
Bioinformatics (Oxford, England)|November 3, 2009
MicroRazerS: rapid alignment of small RNA readsAnne-Katrin Emde, Marcel Grunert, David Weese, et al.
Bioinformatics (Oxford, England)|August 12, 2008
Segment-based multiple sequence alignmentTobias Rausch, Anne-Katrin Emde, David Weese, et al.
Proteome Science|September 26, 2006
Analytical model of peptide mass cluster centres with applicationsWitold E Wolski, Malcolm Farrow, Anne-Katrin Emde, et al.
Bioinformatics (Oxford, England)|March 10, 2009
A consistency-based consensus algorithm for de novo and reference-guided sequence assembly of short readsTobias Rausch, Sergey Koren, Gennady Denisov, et al.
Bioinformatics (Oxford, England)|February 4, 2012
Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end readsRuping Sun, Michael I Love, Tomasz Zemojtel, et al.
Bioinformatics (Oxford, England)|January 13, 2012
Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerSAnne-Katrin Emde, Marcel H Schulz, David Weese, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 3, 2018
Whole Genome Sequencing-Based Discovery of Structural Variants in GlioblastomaKazimierz O Wrzeszczynski, Vanessa Felice, Minita Shah, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
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.
Bioinformatics (Oxford, England)|July 17, 2014
Gustaf: Detecting and correctly classifying SVs in the NGS twilight zoneKathrin Trappe, Anne-Katrin Emde, Hans-Christian Ehrlich, et al.
Genome Research|July 14, 2009
RazerS--fast read mapping with sensitivity controlDavid Weese, Anne-Katrin Emde, Tobias Rausch, et al.
Bioinformatics (Oxford, England)|November 3, 2009
MicroRazerS: rapid alignment of small RNA readsAnne-Katrin Emde, Marcel Grunert, David Weese, et al.
Bioinformatics (Oxford, England)|August 12, 2008
Segment-based multiple sequence alignmentTobias Rausch, Anne-Katrin Emde, David Weese, et al.
Proteome Science|September 26, 2006
Analytical model of peptide mass cluster centres with applicationsWitold E Wolski, Malcolm Farrow, Anne-Katrin Emde, et al.
Bioinformatics (Oxford, England)|March 10, 2009
A consistency-based consensus algorithm for de novo and reference-guided sequence assembly of short readsTobias Rausch, Sergey Koren, Gennady Denisov, et al.
Bioinformatics (Oxford, England)|February 4, 2012
Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end readsRuping Sun, Michael I Love, Tomasz Zemojtel, et al.
Bioinformatics (Oxford, England)|January 13, 2012
Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerSAnne-Katrin Emde, Marcel H Schulz, David Weese, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 3, 2018
Whole Genome Sequencing-Based Discovery of Structural Variants in GlioblastomaKazimierz O Wrzeszczynski, Vanessa Felice, Minita Shah, et al.
Pageof 4