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Niko Popitsch

Showing results (1-10 of 45) with videos related to

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Bioinformatics (Oxford, England)|August 24, 2018
VARAN-GIE: curation of genomic interval setsNiko Popitsch
Bioinformatics (Oxford, England)|May 30, 2014
CODOC: efficient access, analysis and compression of depth of coverage signalsNiko Popitsch
Nucleic Acids Research|October 16, 2012
NGC: lossless and lossy compression of aligned high-throughput sequencing dataNiko Popitsch, Arndt von Haeseler
Bioinformatics (Oxford, England)|December 24, 2024
Rnalib: a Python library for custom transcriptomics analysesNiko Popitsch, Stefan L Ameres
Bioinformatics (Oxford, England)|July 16, 2021
Nanopanel2 calls phased low-frequency variants in Nanopore panel sequencing dataNiko Popitsch, Sandra Preuner, Thomas Lion
Bioinformatics (Oxford, England)|September 9, 2016
ReliableGenome: annotation of genomic regions with high/low variant calling concordanceNiko Popitsch, , Anna Schuh, et al.
Nucleic Acids Research|March 2, 2022
GREEN-DB: a framework for the annotation and prioritization of non-coding regulatory variants from whole-genome sequencing dataEdoardo Giacopuzzi, Niko Popitsch, Jenny C Taylor
RNA Biology|June 13, 2014
Revisiting the coding potential of the E. coli genome through Hfq co-immunoprecipitationIvana Bilusic, Niko Popitsch, Philipp Rescheneder, et al.
Genome Biology|June 25, 2024
Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation frameworkNiko Popitsch, Tobias Neumann, Arndt von Haeseler, et al.
BMC Genomics|January 7, 2017
Temperature-dependent sRNA transcriptome of the Lyme disease spirocheteNiko Popitsch, Ivana Bilusic, Philipp Rescheneder, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Bioinformatics (Oxford, England)|August 24, 2018
VARAN-GIE: curation of genomic interval setsNiko Popitsch
Bioinformatics (Oxford, England)|May 30, 2014
CODOC: efficient access, analysis and compression of depth of coverage signalsNiko Popitsch
Nucleic Acids Research|October 16, 2012
NGC: lossless and lossy compression of aligned high-throughput sequencing dataNiko Popitsch, Arndt von Haeseler
Bioinformatics (Oxford, England)|December 24, 2024
Rnalib: a Python library for custom transcriptomics analysesNiko Popitsch, Stefan L Ameres
Bioinformatics (Oxford, England)|July 16, 2021
Nanopanel2 calls phased low-frequency variants in Nanopore panel sequencing dataNiko Popitsch, Sandra Preuner, Thomas Lion
Bioinformatics (Oxford, England)|September 9, 2016
ReliableGenome: annotation of genomic regions with high/low variant calling concordanceNiko Popitsch, , Anna Schuh, et al.
Nucleic Acids Research|March 2, 2022
GREEN-DB: a framework for the annotation and prioritization of non-coding regulatory variants from whole-genome sequencing dataEdoardo Giacopuzzi, Niko Popitsch, Jenny C Taylor
RNA Biology|June 13, 2014
Revisiting the coding potential of the E. coli genome through Hfq co-immunoprecipitationIvana Bilusic, Niko Popitsch, Philipp Rescheneder, et al.
Genome Biology|June 25, 2024
Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation frameworkNiko Popitsch, Tobias Neumann, Arndt von Haeseler, et al.
BMC Genomics|January 7, 2017
Temperature-dependent sRNA transcriptome of the Lyme disease spirocheteNiko Popitsch, Ivana Bilusic, Philipp Rescheneder, et al.
Pageof 5