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Aaron G Day-Williams

Showing results (1-10 of 27) with videos related to

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European Journal of Clinical Investigation|December 16, 2010
The effect of next-generation sequencing technology on complex trait researchAaron G Day-Williams, Eleftheria Zeggini
Human Heredity|March 24, 2012
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing dataJennifer L Asimit, Aaron G Day-Williams, Andrew P Morris, et al.
Human Heredity|August 9, 2011
Unifying ideas for non-parametric linkage analysisAaron G Day-Williams, John Blangero, Thomas D Dyer, et al.
BMC Bioinformatics|October 23, 2010
CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studiesRobert Lawrence, Aaron G Day-Williams, Katherine S Elliott, et al.
Genetic Epidemiology|April 6, 2011
Linkage analysis without defined pedigreesAaron G Day-Williams, John Blangero, Thomas D Dyer, et al.
Genetic Epidemiology|September 7, 2012
Genome-wide association analysis of imputed rare variants: application to seven common complex diseasesReedik Mägi, Jennifer L Asimit, Aaron G Day-Williams, et al.
BMC Bioinformatics|November 3, 2009
GLIDERS--a web-based search engine for genome-wide linkage disequilibrium between HapMap SNPsRobert Lawrence, Aaron G Day-Williams, Richard Mott, et al.
Journal of Clinical Immunology|November 13, 2014
Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal LeukoencephalopathyAaron G Day-Williams, Chao Sun, Ilijas Jelcic, et al.
Genome Biology|October 26, 2018
PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variantsCorneliu A Bodea, Adele A Mitchell, Alex Bloemendal, et al.
Plos One|November 10, 2011
An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studiesAaron G Day-Williams, Kirsten McLay, Eleanor Drury, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
European Journal of Clinical Investigation|December 16, 2010
The effect of next-generation sequencing technology on complex trait researchAaron G Day-Williams, Eleftheria Zeggini
Human Heredity|March 24, 2012
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing dataJennifer L Asimit, Aaron G Day-Williams, Andrew P Morris, et al.
Human Heredity|August 9, 2011
Unifying ideas for non-parametric linkage analysisAaron G Day-Williams, John Blangero, Thomas D Dyer, et al.
BMC Bioinformatics|October 23, 2010
CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studiesRobert Lawrence, Aaron G Day-Williams, Katherine S Elliott, et al.
Genetic Epidemiology|April 6, 2011
Linkage analysis without defined pedigreesAaron G Day-Williams, John Blangero, Thomas D Dyer, et al.
Genetic Epidemiology|September 7, 2012
Genome-wide association analysis of imputed rare variants: application to seven common complex diseasesReedik Mägi, Jennifer L Asimit, Aaron G Day-Williams, et al.
BMC Bioinformatics|November 3, 2009
GLIDERS--a web-based search engine for genome-wide linkage disequilibrium between HapMap SNPsRobert Lawrence, Aaron G Day-Williams, Richard Mott, et al.
Journal of Clinical Immunology|November 13, 2014
Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal LeukoencephalopathyAaron G Day-Williams, Chao Sun, Ilijas Jelcic, et al.
Genome Biology|October 26, 2018
PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variantsCorneliu A Bodea, Adele A Mitchell, Alex Bloemendal, et al.
Plos One|November 10, 2011
An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studiesAaron G Day-Williams, Kirsten McLay, Eleanor Drury, et al.
Pageof 3