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Adam P Butler

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

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Current Protocols in Bioinformatics|December 19, 2015
VAGrENT: Variation Annotation GeneratorAndy Menzies, Jon W Teague, Adam P Butler, et al.
Current Protocols in Bioinformatics|December 19, 2015
cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End SequencingKeiran M Raine, Jonathan Hinton, Adam P Butler, et al.
Current Protocols in Bioinformatics|December 9, 2016
cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS DataDavid Jones, Keiran M Raine, Helen Davies, et al.
Bioinformatics (Oxford, England)|November 18, 2021
Variant Library Annotation Tool (VaLiAnT): an oligonucleotide library design and annotation tool for saturation genome editing and other deep mutational scanning experimentsLuca Barbon, Victoria Offord, Elizabeth J Radford, et al.
Current Protocols in Bioinformatics|December 9, 2016
ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing DataKeiran M Raine, Peter Van Loo, David C Wedge, et al.
Haematologica|October 26, 2019
RNAmut: robust identification of somatic mutations in acute myeloid leukemia using RNA-sequencingMuxin Gu, Maximillian Zwiebel, Swee Hoe Ong, et al.
Bioinformatics (Oxford, England)|October 31, 2025
SPARKI: a tool for the statistical analysis of pathogen identification resultsJacqueline M Boccacino, Martin Del Castillo Velasco-Herrera, Mathew A Beale, et al.
BMC Genomics|August 15, 2018
Unsupervised correction of gene-independent cell responses to CRISPR-Cas9 targetingFrancesco Iorio, Fiona M Behan, Emanuel Gonçalves, et al.
Database : the Journal of Biological Databases and Curation|May 26, 2011
Data mining using the Catalogue of Somatic Mutations in Cancer BioMartRebecca Shepherd, Simon A Forbes, David Beare, et al.
Nature Genetics|April 15, 2014
Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancerSerena Nik-Zainal, David C Wedge, Ludmil B Alexandrov, et al.
Pageof 4

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

Sort By:
Pageof 4
Current Protocols in Bioinformatics|December 19, 2015
VAGrENT: Variation Annotation GeneratorAndy Menzies, Jon W Teague, Adam P Butler, et al.
Current Protocols in Bioinformatics|December 19, 2015
cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End SequencingKeiran M Raine, Jonathan Hinton, Adam P Butler, et al.
Current Protocols in Bioinformatics|December 9, 2016
cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS DataDavid Jones, Keiran M Raine, Helen Davies, et al.
Bioinformatics (Oxford, England)|November 18, 2021
Variant Library Annotation Tool (VaLiAnT): an oligonucleotide library design and annotation tool for saturation genome editing and other deep mutational scanning experimentsLuca Barbon, Victoria Offord, Elizabeth J Radford, et al.
Current Protocols in Bioinformatics|December 9, 2016
ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing DataKeiran M Raine, Peter Van Loo, David C Wedge, et al.
Haematologica|October 26, 2019
RNAmut: robust identification of somatic mutations in acute myeloid leukemia using RNA-sequencingMuxin Gu, Maximillian Zwiebel, Swee Hoe Ong, et al.
Bioinformatics (Oxford, England)|October 31, 2025
SPARKI: a tool for the statistical analysis of pathogen identification resultsJacqueline M Boccacino, Martin Del Castillo Velasco-Herrera, Mathew A Beale, et al.
BMC Genomics|August 15, 2018
Unsupervised correction of gene-independent cell responses to CRISPR-Cas9 targetingFrancesco Iorio, Fiona M Behan, Emanuel Gonçalves, et al.
Database : the Journal of Biological Databases and Curation|May 26, 2011
Data mining using the Catalogue of Somatic Mutations in Cancer BioMartRebecca Shepherd, Simon A Forbes, David Beare, et al.
Nature Genetics|April 15, 2014
Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancerSerena Nik-Zainal, David C Wedge, Ludmil B Alexandrov, et al.
Pageof 4