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Stephen W Hartley

Showing results (1-10 of 29) with videos related to

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Bioinformatics (Oxford, England)|February 20, 2013
PleioGRiP: genetic risk prediction with pleiotropyStephen W Hartley, Paola Sebastiani
BMC Bioinformatics|July 19, 2015
QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experimentsStephen W Hartley, James C Mullikin
Nucleic Acids Research|June 4, 2016
Detection and visualization of differential splicing in RNA-Seq data with JunctionSeqStephen W Hartley, James C Mullikin
Frontiers in Genetics|September 14, 2012
Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk predictionStephen W Hartley, Stefano Monti, Ching-Ti Liu, et al.
Plos One|September 30, 2016
Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural RegulationStephen W Hartley, James C Mullikin, David C Klein, et al.
BMC Genetics|December 15, 2010
Clustering by genetic ancestry using genome-wide SNP dataNadia Solovieff, Stephen W Hartley, Clinton T Baldwin, et al.
Plos One|September 15, 2015
Neurotranscriptomics: The Effects of Neonatal Stimulus Deprivation on the Rat Pineal TranscriptomeStephen W Hartley, Steven L Coon, Luis E Savastano, et al.
BMC Genetics|December 17, 2008
Imputation of missing genotypes: an empirical evaluation of IMPUTEZhenming Zhao, Nadia Timofeev, Stephen W Hartley, et al.
Journal of the National Cancer Institute|September 9, 2025
Germline rare variants in cancer susceptibility genes and subsequent neoplasm risk after childhood cancerShahriar A Zamani, Danielle M Karyadi, Stephen W Hartley, et al.
JNCI Cancer Spectrum|March 21, 2026
Homologous recombination repair germline variants and subsequent neoplasm risk among childhood cancer survivorsShahriar A Zamani, Danielle M Karyadi, Stephen W Hartley, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Bioinformatics (Oxford, England)|February 20, 2013
PleioGRiP: genetic risk prediction with pleiotropyStephen W Hartley, Paola Sebastiani
BMC Bioinformatics|July 19, 2015
QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experimentsStephen W Hartley, James C Mullikin
Nucleic Acids Research|June 4, 2016
Detection and visualization of differential splicing in RNA-Seq data with JunctionSeqStephen W Hartley, James C Mullikin
Frontiers in Genetics|September 14, 2012
Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk predictionStephen W Hartley, Stefano Monti, Ching-Ti Liu, et al.
Plos One|September 30, 2016
Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural RegulationStephen W Hartley, James C Mullikin, David C Klein, et al.
BMC Genetics|December 15, 2010
Clustering by genetic ancestry using genome-wide SNP dataNadia Solovieff, Stephen W Hartley, Clinton T Baldwin, et al.
Plos One|September 15, 2015
Neurotranscriptomics: The Effects of Neonatal Stimulus Deprivation on the Rat Pineal TranscriptomeStephen W Hartley, Steven L Coon, Luis E Savastano, et al.
BMC Genetics|December 17, 2008
Imputation of missing genotypes: an empirical evaluation of IMPUTEZhenming Zhao, Nadia Timofeev, Stephen W Hartley, et al.
Journal of the National Cancer Institute|September 9, 2025
Germline rare variants in cancer susceptibility genes and subsequent neoplasm risk after childhood cancerShahriar A Zamani, Danielle M Karyadi, Stephen W Hartley, et al.
JNCI Cancer Spectrum|March 21, 2026
Homologous recombination repair germline variants and subsequent neoplasm risk among childhood cancer survivorsShahriar A Zamani, Danielle M Karyadi, Stephen W Hartley, et al.
Pageof 3