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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
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.
Genome Research|January 17, 2003
The phusion assemblerJames C Mullikin, Zemin Ning
Human Molecular Genetics|August 14, 2010
Exome sequencing: the sweet spot before whole genomesJamie K Teer, James C Mullikin
Genome Biology|February 18, 2010
Genomic features defining exonic variants that modulate splicingAdam Woolfe, James C Mullikin, Laura Elnitski
Bioinformatics (Oxford, England)|February 20, 2013
PleioGRiP: genetic risk prediction with pleiotropyStephen W Hartley, Paola Sebastiani
Clinical Chemistry|February 6, 2016
Systematic Evaluation of Sanger Validation of Next-Generation Sequencing VariantsTyler F Beck, James C Mullikin, , et al.
Molecular Phylogenetics and Evolution|December 19, 2012
A scalable and flexible approach for investigating the genomic landscapes of phylogenetic incongruenceArjun B Prasad, James C Mullikin, , et al.
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