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Peter J Tonellato

Showing results (1-10 of 53) with videos related to

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F1000 Medicine Reports|July 18, 2012
The future of genomics in pathologyDennis P Wall, Peter J Tonellato
Personalized Medicine|May 16, 2018
Deriving clinical action from whole-genome analysisDennis P Wall, Peter J Tonellato
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|December 5, 2013
Analysis of sequence-based copy number variation detection tools for cancer studiesSheida Nabavi, Zhengqiu Cai, Peter J Tonellato
Methods in Cell Biology|December 18, 2004
Automated analysis of conserved syntenies for the zebrafish genomeJohn Postlethwait, Victor Ruotti, Michael J Carvan, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|March 9, 2017
Optimal decision support rules improve personalize warfarin treatment outcomesChih-Lin Chi, Kourosh Ravvaz, John Weissert, et al.
Future Virology|March 24, 2022
A community call to action: mitigating COVID pandemic's impact on mental healthWahid Ullah, Muhammad Ilyas, Mukhtar Alam, et al.
BMC Bioinformatics|January 22, 2017
MC-GenomeKey: a multicloud system for the detection and annotation of genomic variantsHatem Elshazly, Yassine Souilmi, Peter J Tonellato, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 9, 2017
Using simulation and optimization approach to improve outcome through warfarin precision treatmentChih-Lin Chi, Lu He, Kourosh Ravvaz, et al.
American Journal of Clinical Pathology|April 20, 2011
A national agenda for the future of pathology in personalized medicine: report of the proceedings of a meeting at the Banbury Conference Center on genome-era pathology, precision diagnostics, and preemptive care: a stakeholder summitPeter J Tonellato, James M Crawford, Mark S Boguski, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
Ultradense array CGH and discovery of micro-copy number alterations and gene fusions in the cancer genomeEwa Przybytkowski, Adriana Aguilar-Mahecha, Sheida Nabavi, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
F1000 Medicine Reports|July 18, 2012
The future of genomics in pathologyDennis P Wall, Peter J Tonellato
Personalized Medicine|May 16, 2018
Deriving clinical action from whole-genome analysisDennis P Wall, Peter J Tonellato
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|December 5, 2013
Analysis of sequence-based copy number variation detection tools for cancer studiesSheida Nabavi, Zhengqiu Cai, Peter J Tonellato
Methods in Cell Biology|December 18, 2004
Automated analysis of conserved syntenies for the zebrafish genomeJohn Postlethwait, Victor Ruotti, Michael J Carvan, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|March 9, 2017
Optimal decision support rules improve personalize warfarin treatment outcomesChih-Lin Chi, Kourosh Ravvaz, John Weissert, et al.
Future Virology|March 24, 2022
A community call to action: mitigating COVID pandemic's impact on mental healthWahid Ullah, Muhammad Ilyas, Mukhtar Alam, et al.
BMC Bioinformatics|January 22, 2017
MC-GenomeKey: a multicloud system for the detection and annotation of genomic variantsHatem Elshazly, Yassine Souilmi, Peter J Tonellato, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 9, 2017
Using simulation and optimization approach to improve outcome through warfarin precision treatmentChih-Lin Chi, Lu He, Kourosh Ravvaz, et al.
American Journal of Clinical Pathology|April 20, 2011
A national agenda for the future of pathology in personalized medicine: report of the proceedings of a meeting at the Banbury Conference Center on genome-era pathology, precision diagnostics, and preemptive care: a stakeholder summitPeter J Tonellato, James M Crawford, Mark S Boguski, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
Ultradense array CGH and discovery of micro-copy number alterations and gene fusions in the cancer genomeEwa Przybytkowski, Adriana Aguilar-Mahecha, Sheida Nabavi, et al.
Pageof 6