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Andrew Lonie

Showing results (1-10 of 24) with videos related to

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Proceedings of XSEDE16 : Diversity, Big Data, and Science at Scale : July 17-21, 2016, Intercontinental Miami Hotel, Miami, Florida, USA. Conference on Extreme Science and Engineering Discovery Environment (5Th : 2016 : Miami, Fla.)|August 23, 2021
CloudBridge: a Simple Cross-Cloud Python LibraryNuwan Goonasekera, Andrew Lonie, James Taylor, et al.
Future Generations Computer Systems : FGCS|August 9, 2021
CloudLaunch: Discover and Deploy Cloud ApplicationsEnis Afgan, Andrew Lonie, James Taylor, et al.
BMC Bioinformatics|July 14, 2017
Investigating reproducibility and tracking provenance - A genomic workflow case studySehrish Kanwal, Farah Zaib Khan, Andrew Lonie, et al.
Journal of Extracellular Vesicles|November 13, 2015
iSRAP - a one-touch research tool for rapid profiling of small RNA-seq dataCamelia Quek, Chol-Hee Jung, Shayne A Bellingham, et al.
Gigascience|November 2, 2019
Sharing interoperable workflow provenance: A review of best practices and their practical application in CWLProvFarah Zaib Khan, Stian Soiland-Reyes, Richard O Sinnott, et al.
Parasites & Vectors|March 18, 2016
Pipeline for the identification and classification of ion channels in parasitic flatwormsBahiyah Nor, Neil D Young, Pasi K Korhonen, et al.
Parasites & Vectors|June 3, 2014
Identification of G protein-coupled receptors in Schistosoma haematobium and S. mansoni by comparative genomicsTulio D L Campos, Neil D Young, Pasi K Korhonen, et al.
Plos One|October 27, 2015
Genomics Virtual Laboratory: A Practical Bioinformatics Workbench for the CloudEnis Afgan, Clare Sloggett, Nuwan Goonasekera, et al.
Breast Cancer Research and Treatment|November 20, 2014
Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancerGianluca Severi, Melissa C Southey, Dallas R English, et al.
BMC Bioinformatics|February 28, 2013
FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasetsBernard J Pope, Tú Nguyen-Dumont, Fabrice Odefrey, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Proceedings of XSEDE16 : Diversity, Big Data, and Science at Scale : July 17-21, 2016, Intercontinental Miami Hotel, Miami, Florida, USA. Conference on Extreme Science and Engineering Discovery Environment (5Th : 2016 : Miami, Fla.)|August 23, 2021
CloudBridge: a Simple Cross-Cloud Python LibraryNuwan Goonasekera, Andrew Lonie, James Taylor, et al.
Future Generations Computer Systems : FGCS|August 9, 2021
CloudLaunch: Discover and Deploy Cloud ApplicationsEnis Afgan, Andrew Lonie, James Taylor, et al.
BMC Bioinformatics|July 14, 2017
Investigating reproducibility and tracking provenance - A genomic workflow case studySehrish Kanwal, Farah Zaib Khan, Andrew Lonie, et al.
Journal of Extracellular Vesicles|November 13, 2015
iSRAP - a one-touch research tool for rapid profiling of small RNA-seq dataCamelia Quek, Chol-Hee Jung, Shayne A Bellingham, et al.
Gigascience|November 2, 2019
Sharing interoperable workflow provenance: A review of best practices and their practical application in CWLProvFarah Zaib Khan, Stian Soiland-Reyes, Richard O Sinnott, et al.
Parasites & Vectors|March 18, 2016
Pipeline for the identification and classification of ion channels in parasitic flatwormsBahiyah Nor, Neil D Young, Pasi K Korhonen, et al.
Parasites & Vectors|June 3, 2014
Identification of G protein-coupled receptors in Schistosoma haematobium and S. mansoni by comparative genomicsTulio D L Campos, Neil D Young, Pasi K Korhonen, et al.
Plos One|October 27, 2015
Genomics Virtual Laboratory: A Practical Bioinformatics Workbench for the CloudEnis Afgan, Clare Sloggett, Nuwan Goonasekera, et al.
Breast Cancer Research and Treatment|November 20, 2014
Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancerGianluca Severi, Melissa C Southey, Dallas R English, et al.
BMC Bioinformatics|February 28, 2013
FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasetsBernard J Pope, Tú Nguyen-Dumont, Fabrice Odefrey, et al.
Pageof 3