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Venkatraman E Seshan

Showing results (1-10 of 106) with videos related to

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Nucleic Acids Research|June 9, 2016
FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencingRonglai Shen, Venkatraman E Seshan
Genetic Epidemiology|January 6, 2015
False discovery rates for rare variants from sequenced dataMarinela Capanu, Venkatraman E Seshan
Methods in Molecular Biology (Clifton, N.J.)|February 7, 2012
Multi-SNP haplotype analysis methods for association analysisDaniel O Stram, Venkatraman E Seshan
Methods in Molecular Biology (Clifton, N.J.)|June 25, 2022
FACETS: Fraction and Allele-Specific Copy Number Estimates from Tumor SequencingArshi Arora, Ronglai Shen, Venkatraman E Seshan
Clinical Trials (London, England)|July 25, 2013
Testing the incremental predictive accuracy of new markersColin B Begg, Mithat Gonen, Venkatraman E Seshan
Biometrics|February 13, 2008
Comparison of properties of tests for assessing tumor clonalityIrina Ostrovnaya, Venkatraman E Seshan, Colin B Begg
The Annals of Applied Statistics|November 24, 2015
USING SOMATIC MUTATION DATA TO TEST TUMORS FOR CLONAL RELATEDNESSIrina Ostrovnaya, Venkatraman E Seshan, Colin B Begg
Statistics in Medicine|October 5, 2012
Comparing ROC curves derived from regression modelsVenkatraman E Seshan, Mithat Gönen, Colin B Begg
American Journal of Epidemiology|March 13, 2018
RE: "A MULTINOMIAL REGRESSION APPROACH TO MODEL OUTCOME HETEROGENEITY"Colin B Begg, Venkatraman E Seshan, Emily C Zabor
Genome Medicine|December 4, 2020
Pan-cancer identification of clinically relevant genomic subtypes using outcome-weighted integrative clusteringArshi Arora, Adam B Olshen, Venkatraman E Seshan, et al.
Pageof 11

Showing results (1-10 of 106) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|June 9, 2016
FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencingRonglai Shen, Venkatraman E Seshan
Genetic Epidemiology|January 6, 2015
False discovery rates for rare variants from sequenced dataMarinela Capanu, Venkatraman E Seshan
Methods in Molecular Biology (Clifton, N.J.)|February 7, 2012
Multi-SNP haplotype analysis methods for association analysisDaniel O Stram, Venkatraman E Seshan
Methods in Molecular Biology (Clifton, N.J.)|June 25, 2022
FACETS: Fraction and Allele-Specific Copy Number Estimates from Tumor SequencingArshi Arora, Ronglai Shen, Venkatraman E Seshan
Clinical Trials (London, England)|July 25, 2013
Testing the incremental predictive accuracy of new markersColin B Begg, Mithat Gonen, Venkatraman E Seshan
Biometrics|February 13, 2008
Comparison of properties of tests for assessing tumor clonalityIrina Ostrovnaya, Venkatraman E Seshan, Colin B Begg
The Annals of Applied Statistics|November 24, 2015
USING SOMATIC MUTATION DATA TO TEST TUMORS FOR CLONAL RELATEDNESSIrina Ostrovnaya, Venkatraman E Seshan, Colin B Begg
Statistics in Medicine|October 5, 2012
Comparing ROC curves derived from regression modelsVenkatraman E Seshan, Mithat Gönen, Colin B Begg
American Journal of Epidemiology|March 13, 2018
RE: "A MULTINOMIAL REGRESSION APPROACH TO MODEL OUTCOME HETEROGENEITY"Colin B Begg, Venkatraman E Seshan, Emily C Zabor
Genome Medicine|December 4, 2020
Pan-cancer identification of clinically relevant genomic subtypes using outcome-weighted integrative clusteringArshi Arora, Adam B Olshen, Venkatraman E Seshan, et al.
Pageof 11