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Stephan Ossowski

Showing results (41-50 of 155) with videos related to

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Open Biology|July 30, 2025
Long-read RNA-sequencing reveals transcript-specific regulation in human-derived cortical neuronsJishu Xu, Michaela Hörner, Elena Buena Atienza, et al.
BMC Genomics|November 12, 2017
Genomic characterisation of clinical and environmental Pseudomonas putida group strains and determination of their role in the transfer of antimicrobial resistance genes to Pseudomonas aeruginosaSilke Peter, Philipp Oberhettinger, Leonard Schuele, et al.
Evolution; International Journal of Organic Evolution|June 10, 2014
A shift from magnitude to sign epistasis during adaptive evolution of a bacterial social traitPeter C Zee, Helena Mendes-Soares, Yuen-Tsu N Yu, et al.
Molecular Cell|January 27, 2015
Chromatin-wide profiling of DYRK1A reveals a role as a gene-specific RNA polymerase II CTD kinaseChiara Di Vona, Daniela Bezdan, Abul B M M K Islam, et al.
Nature Methods|August 1, 2009
SHOREmap: simultaneous mapping and mutation identification by deep sequencingKorbinian Schneeberger, Stephan Ossowski, Christa Lanz, et al.
Clinical and Translational Radiation Oncology|December 13, 2024
Tumor sequencing before and after neoadjuvant chemoradiotherapy in locally advanced rectal cancer: Genetic tumor characterization and clinical outcomeKerstin Clasen, Nadja Ballin, Leon Schütz, et al.
European Journal of Human Genetics : EJHG|May 31, 2024
Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomesGerman Demidov, Steven Laurie, Annalaura Torella, et al.
European Journal of Human Genetics : EJHG|April 8, 2025
Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomesGerman Demidov, Steven Laurie, Annalaura Torella, et al.
Human Mutation|October 25, 2018
Allele balance bias identifies systematic genotyping errors and false disease associationsFrancesc Muyas, Mattia Bosio, Anna Puig, et al.
Molecular Genetics & Genomic Medicine|September 7, 2021
Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing dataGerman Demidov, Joohyun Park, Sorin Armeanu-Ebinger, et al.
Pageof 16

Showing results (41-50 of 155) with videos related to

Sort By:
Pageof 16
Open Biology|July 30, 2025
Long-read RNA-sequencing reveals transcript-specific regulation in human-derived cortical neuronsJishu Xu, Michaela Hörner, Elena Buena Atienza, et al.
BMC Genomics|November 12, 2017
Genomic characterisation of clinical and environmental Pseudomonas putida group strains and determination of their role in the transfer of antimicrobial resistance genes to Pseudomonas aeruginosaSilke Peter, Philipp Oberhettinger, Leonard Schuele, et al.
Evolution; International Journal of Organic Evolution|June 10, 2014
A shift from magnitude to sign epistasis during adaptive evolution of a bacterial social traitPeter C Zee, Helena Mendes-Soares, Yuen-Tsu N Yu, et al.
Molecular Cell|January 27, 2015
Chromatin-wide profiling of DYRK1A reveals a role as a gene-specific RNA polymerase II CTD kinaseChiara Di Vona, Daniela Bezdan, Abul B M M K Islam, et al.
Nature Methods|August 1, 2009
SHOREmap: simultaneous mapping and mutation identification by deep sequencingKorbinian Schneeberger, Stephan Ossowski, Christa Lanz, et al.
Clinical and Translational Radiation Oncology|December 13, 2024
Tumor sequencing before and after neoadjuvant chemoradiotherapy in locally advanced rectal cancer: Genetic tumor characterization and clinical outcomeKerstin Clasen, Nadja Ballin, Leon Schütz, et al.
European Journal of Human Genetics : EJHG|May 31, 2024
Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomesGerman Demidov, Steven Laurie, Annalaura Torella, et al.
European Journal of Human Genetics : EJHG|April 8, 2025
Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomesGerman Demidov, Steven Laurie, Annalaura Torella, et al.
Human Mutation|October 25, 2018
Allele balance bias identifies systematic genotyping errors and false disease associationsFrancesc Muyas, Mattia Bosio, Anna Puig, et al.
Molecular Genetics & Genomic Medicine|September 7, 2021
Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing dataGerman Demidov, Joohyun Park, Sorin Armeanu-Ebinger, et al.
Pageof 16