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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 detection
Dorota H Sendorek, Cristian Caloian, Kyle Ellrott, et al.
Genome Biology
|
September 12, 2019
Reproducible biomedical benchmarking in the cloud: lessons from crowd-sourced data challenges
Kyle 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 Pipelines
Kyle Ellrott, Matthew H Bailey, Gordon Saksena, et al.
BMC Bioinformatics
|
September 27, 2018
Valection: design optimization for validation and verification studies
Christopher 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 Portal
Yulia Newton, Adam M Novak, Teresa Swatloski, et al.
STAR Protocols
|
April 9, 2025
Protocol for obtaining cancer type and subtype predictions using subSCOPE
Jasleen 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 challenge
Paul 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 samples
Matthew 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 samples
Matthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.
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Search research articles
Search
Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 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 detection
Dorota H Sendorek, Cristian Caloian, Kyle Ellrott, et al.
Genome Biology
|
September 12, 2019
Reproducible biomedical benchmarking in the cloud: lessons from crowd-sourced data challenges
Kyle 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 Pipelines
Kyle Ellrott, Matthew H Bailey, Gordon Saksena, et al.
BMC Bioinformatics
|
September 27, 2018
Valection: design optimization for validation and verification studies
Christopher 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 Portal
Yulia Newton, Adam M Novak, Teresa Swatloski, et al.
STAR Protocols
|
April 9, 2025
Protocol for obtaining cancer type and subtype predictions using subSCOPE
Jasleen 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 challenge
Paul 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 samples
Matthew 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 samples
Matthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.
Page
of 6