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Benedict Paten

Showing results (81-90 of 203) with videos related to

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NAR Genomics and Bioinformatics|April 13, 2026
Lancet2: Improved and accelerated somatic variant calling with joint multi-sample local assembly graphsRajeeva Lochan Musunuri, Bryan Zhu, Wayne E Clarke, et al.
Genome Research|May 10, 2023
Gaps and complex structurally variant loci in phased genome assembliesDavid Porubsky, Mitchell R Vollger, William T Harvey, et al.
Journal of Biomedical Informatics|May 15, 2017
Developing a framework for digital objects in the Big Data to Knowledge (BD2K) commons: Report from the Commons Framework Pilots workshopKathleen M Jagodnik, Simon Koplev, Sherry L Jenkins, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Pangenome-aware DeepVariantMobin Asri, Pi-Chuan Chang, Juan Carlos Mier, et al.
Annual Review of Genomics and Human Genetics|May 27, 2020
Pangenome GraphsJordan M Eizenga, Adam M Novak, Jonas A Sibbesen, et al.
Nucleic Acids Research|May 12, 2021
The Dockstore: enhancing a community platform for sharing reproducible and accessible computational protocolsDenis Yuen, Louise Cabansay, Andrew Duncan, et al.
Research Square|November 24, 2025
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffeXian Chang, Adam M Novak, Jordan M Eizenga, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffeXian Chang, Adam M Novak, Jordan M Eizenga, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
A Pan-pangenome illuminates complex structural variation and selection in humans, chimpanzees, and bonobosJoana Rocha, Runyang Nicolas Lou, Carolina De Lima Adam, et al.
Biorxiv : the Preprint Server for Biology|October 1, 2025
Diploid genome assembly of human fibroblast cell lines enables clone specific variant calling, improved read mapping and accurate phasingT Rhyker Ranallo-Benavidez, Yue Hao, Emilia Volpe, et al.
Pageof 21

Showing results (81-90 of 203) with videos related to

Sort By:
Pageof 21
NAR Genomics and Bioinformatics|April 13, 2026
Lancet2: Improved and accelerated somatic variant calling with joint multi-sample local assembly graphsRajeeva Lochan Musunuri, Bryan Zhu, Wayne E Clarke, et al.
Genome Research|May 10, 2023
Gaps and complex structurally variant loci in phased genome assembliesDavid Porubsky, Mitchell R Vollger, William T Harvey, et al.
Journal of Biomedical Informatics|May 15, 2017
Developing a framework for digital objects in the Big Data to Knowledge (BD2K) commons: Report from the Commons Framework Pilots workshopKathleen M Jagodnik, Simon Koplev, Sherry L Jenkins, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Pangenome-aware DeepVariantMobin Asri, Pi-Chuan Chang, Juan Carlos Mier, et al.
Annual Review of Genomics and Human Genetics|May 27, 2020
Pangenome GraphsJordan M Eizenga, Adam M Novak, Jonas A Sibbesen, et al.
Nucleic Acids Research|May 12, 2021
The Dockstore: enhancing a community platform for sharing reproducible and accessible computational protocolsDenis Yuen, Louise Cabansay, Andrew Duncan, et al.
Research Square|November 24, 2025
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffeXian Chang, Adam M Novak, Jordan M Eizenga, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffeXian Chang, Adam M Novak, Jordan M Eizenga, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
A Pan-pangenome illuminates complex structural variation and selection in humans, chimpanzees, and bonobosJoana Rocha, Runyang Nicolas Lou, Carolina De Lima Adam, et al.
Biorxiv : the Preprint Server for Biology|October 1, 2025
Diploid genome assembly of human fibroblast cell lines enables clone specific variant calling, improved read mapping and accurate phasingT Rhyker Ranallo-Benavidez, Yue Hao, Emilia Volpe, et al.
Pageof 21