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Bioinformatics (Oxford, England)
|
August 24, 2018
VARAN-GIE: curation of genomic interval sets
Niko Popitsch
Bioinformatics (Oxford, England)
|
May 30, 2014
CODOC: efficient access, analysis and compression of depth of coverage signals
Niko Popitsch
Nucleic Acids Research
|
October 16, 2012
NGC: lossless and lossy compression of aligned high-throughput sequencing data
Niko Popitsch, Arndt von Haeseler
Bioinformatics (Oxford, England)
|
December 24, 2024
Rnalib: a Python library for custom transcriptomics analyses
Niko Popitsch, Stefan L Ameres
Bioinformatics (Oxford, England)
|
July 16, 2021
Nanopanel2 calls phased low-frequency variants in Nanopore panel sequencing data
Niko Popitsch, Sandra Preuner, Thomas Lion
Bioinformatics (Oxford, England)
|
September 9, 2016
ReliableGenome: annotation of genomic regions with high/low variant calling concordance
Niko 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 data
Edoardo Giacopuzzi, Niko Popitsch, Jenny C Taylor
RNA Biology
|
June 13, 2014
Revisiting the coding potential of the E. coli genome through Hfq co-immunoprecipitation
Ivana Bilusic, Niko Popitsch, Philipp Rescheneder, et al.
Genome Biology
|
June 25, 2024
Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework
Niko Popitsch, Tobias Neumann, Arndt von Haeseler, et al.
BMC Genomics
|
January 7, 2017
Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
Niko Popitsch, Ivana Bilusic, Philipp Rescheneder, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Bioinformatics (Oxford, England)
|
August 24, 2018
VARAN-GIE: curation of genomic interval sets
Niko Popitsch
Bioinformatics (Oxford, England)
|
May 30, 2014
CODOC: efficient access, analysis and compression of depth of coverage signals
Niko Popitsch
Nucleic Acids Research
|
October 16, 2012
NGC: lossless and lossy compression of aligned high-throughput sequencing data
Niko Popitsch, Arndt von Haeseler
Bioinformatics (Oxford, England)
|
December 24, 2024
Rnalib: a Python library for custom transcriptomics analyses
Niko Popitsch, Stefan L Ameres
Bioinformatics (Oxford, England)
|
July 16, 2021
Nanopanel2 calls phased low-frequency variants in Nanopore panel sequencing data
Niko Popitsch, Sandra Preuner, Thomas Lion
Bioinformatics (Oxford, England)
|
September 9, 2016
ReliableGenome: annotation of genomic regions with high/low variant calling concordance
Niko 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 data
Edoardo Giacopuzzi, Niko Popitsch, Jenny C Taylor
RNA Biology
|
June 13, 2014
Revisiting the coding potential of the E. coli genome through Hfq co-immunoprecipitation
Ivana Bilusic, Niko Popitsch, Philipp Rescheneder, et al.
Genome Biology
|
June 25, 2024
Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework
Niko Popitsch, Tobias Neumann, Arndt von Haeseler, et al.
BMC Genomics
|
January 7, 2017
Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
Niko Popitsch, Ivana Bilusic, Philipp Rescheneder, et al.
Page
of 5