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Bioinformatics (Oxford, England)
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February 20, 2013
PleioGRiP: genetic risk prediction with pleiotropy
Stephen W Hartley, Paola Sebastiani
BMC Bioinformatics
|
July 19, 2015
QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments
Stephen W Hartley, James C Mullikin
Nucleic Acids Research
|
June 4, 2016
Detection and visualization of differential splicing in RNA-Seq data with JunctionSeq
Stephen W Hartley, James C Mullikin
Frontiers in Genetics
|
September 14, 2012
Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction
Stephen 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 Regulation
Stephen W Hartley, James C Mullikin, David C Klein, et al.
BMC Genetics
|
December 15, 2010
Clustering by genetic ancestry using genome-wide SNP data
Nadia 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 Transcriptome
Stephen W Hartley, Steven L Coon, Luis E Savastano, et al.
BMC Genetics
|
December 17, 2008
Imputation of missing genotypes: an empirical evaluation of IMPUTE
Zhenming 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 cancer
Shahriar 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 survivors
Shahriar A Zamani, Danielle M Karyadi, Stephen W Hartley, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Bioinformatics (Oxford, England)
|
February 20, 2013
PleioGRiP: genetic risk prediction with pleiotropy
Stephen W Hartley, Paola Sebastiani
BMC Bioinformatics
|
July 19, 2015
QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments
Stephen W Hartley, James C Mullikin
Nucleic Acids Research
|
June 4, 2016
Detection and visualization of differential splicing in RNA-Seq data with JunctionSeq
Stephen W Hartley, James C Mullikin
Frontiers in Genetics
|
September 14, 2012
Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction
Stephen 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 Regulation
Stephen W Hartley, James C Mullikin, David C Klein, et al.
BMC Genetics
|
December 15, 2010
Clustering by genetic ancestry using genome-wide SNP data
Nadia 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 Transcriptome
Stephen W Hartley, Steven L Coon, Luis E Savastano, et al.
BMC Genetics
|
December 17, 2008
Imputation of missing genotypes: an empirical evaluation of IMPUTE
Zhenming 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 cancer
Shahriar 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 survivors
Shahriar A Zamani, Danielle M Karyadi, Stephen W Hartley, et al.
Page
of 3