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Kyle Ellrott

Showing results (21-30 of 56) with videos related to

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Nature Genetics|September 28, 2013
The Cancer Genome Atlas Pan-Cancer analysis project, John N Weinstein, Eric A Collisson, et al.
BMC Bioinformatics|February 2, 2018
Germline contamination and leakage in whole genome somatic single nucleotide variant detectionDorota H Sendorek, Cristian Caloian, Kyle Ellrott, et al.
Genome Biology|September 12, 2019
Reproducible biomedical benchmarking in the cloud: lessons from crowd-sourced data challengesKyle Ellrott, Alex Buchanan, Allison Creason, et al.
Cell Systems|March 30, 2018
Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic PipelinesKyle Ellrott, Matthew H Bailey, Gordon Saksena, et al.
BMC Bioinformatics|September 27, 2018
Valection: design optimization for validation and verification studiesChristopher I Cooper, Delia Yao, Dorota H Sendorek, et al.
Cancer Research|November 3, 2017
TumorMap: Exploring the Molecular Similarities of Cancer Samples in an Interactive PortalYulia Newton, Adam M Novak, Teresa Swatloski, et al.
STAR Protocols|April 9, 2025
Protocol for obtaining cancer type and subtype predictions using subSCOPEJasleen K Grewal, A Gordon Robertson, Kyle Ellrott, et al.
Nature Genetics|March 29, 2014
Global optimization of somatic variant identification in cancer genomes with a global community challengePaul C Boutros, Adam D Ewing, Kyle Ellrott, et al.
Nature Communications|September 22, 2020
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samplesMatthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.
Nature Communications|December 1, 2020
Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samplesMatthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Nature Genetics|September 28, 2013
The Cancer Genome Atlas Pan-Cancer analysis project, John N Weinstein, Eric A Collisson, et al.
BMC Bioinformatics|February 2, 2018
Germline contamination and leakage in whole genome somatic single nucleotide variant detectionDorota H Sendorek, Cristian Caloian, Kyle Ellrott, et al.
Genome Biology|September 12, 2019
Reproducible biomedical benchmarking in the cloud: lessons from crowd-sourced data challengesKyle Ellrott, Alex Buchanan, Allison Creason, et al.
Cell Systems|March 30, 2018
Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic PipelinesKyle Ellrott, Matthew H Bailey, Gordon Saksena, et al.
BMC Bioinformatics|September 27, 2018
Valection: design optimization for validation and verification studiesChristopher I Cooper, Delia Yao, Dorota H Sendorek, et al.
Cancer Research|November 3, 2017
TumorMap: Exploring the Molecular Similarities of Cancer Samples in an Interactive PortalYulia Newton, Adam M Novak, Teresa Swatloski, et al.
STAR Protocols|April 9, 2025
Protocol for obtaining cancer type and subtype predictions using subSCOPEJasleen K Grewal, A Gordon Robertson, Kyle Ellrott, et al.
Nature Genetics|March 29, 2014
Global optimization of somatic variant identification in cancer genomes with a global community challengePaul C Boutros, Adam D Ewing, Kyle Ellrott, et al.
Nature Communications|September 22, 2020
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samplesMatthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.
Nature Communications|December 1, 2020
Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samplesMatthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.
Pageof 6