Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alison J Coffey

Showing results (1-10 of 39) with videos related to

Pageof 4
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|September 6, 2003
DNA rescue by the vectorette methodMarcia A McAleer, Alison J Coffey, Ian Dunham
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.
Plos One|December 5, 2012
A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profilingChristine Clark, Priit Palta, Christopher J Joyce, et al.
Pharmacogenetics and Genomics|May 19, 2006
Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistanceGuy Leschziner, Delilah Zabaneh, M Pirmohamed, et al.
Nature Methods|January 30, 2010
Target-enrichment strategies for next-generation sequencingLira Mamanova, Alison J Coffey, Carol E Scott, et al.
American Journal of Human Genetics|March 10, 2005
Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genomePawandeep Dhami, Alison J Coffey, Stephen Abbs, et al.
Pharmacogenetics and Genomics|April 27, 2007
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approachGuy D Leschziner, Toby Andrew, John Paul Leach, et al.
Blood|October 26, 2013
Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regionsMatthias Zilbauer, Tim F Rayner, Christine Clark, et al.
Basic Research in Cardiology|May 7, 2013
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotypeMaren M Limberg, Sven Zumhagen, Michael F Netter, et al.
European Journal of Human Genetics : EJHG|April 2, 2024
A framework for the evaluation and reporting of incidental findings in clinical genomic testingCarolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Methods in Molecular Biology (Clifton, N.J.)|September 6, 2003
DNA rescue by the vectorette methodMarcia A McAleer, Alison J Coffey, Ian Dunham
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.
Plos One|December 5, 2012
A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profilingChristine Clark, Priit Palta, Christopher J Joyce, et al.
Pharmacogenetics and Genomics|May 19, 2006
Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistanceGuy Leschziner, Delilah Zabaneh, M Pirmohamed, et al.
Nature Methods|January 30, 2010
Target-enrichment strategies for next-generation sequencingLira Mamanova, Alison J Coffey, Carol E Scott, et al.
American Journal of Human Genetics|March 10, 2005
Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genomePawandeep Dhami, Alison J Coffey, Stephen Abbs, et al.
Pharmacogenetics and Genomics|April 27, 2007
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approachGuy D Leschziner, Toby Andrew, John Paul Leach, et al.
Blood|October 26, 2013
Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regionsMatthias Zilbauer, Tim F Rayner, Christine Clark, et al.
Basic Research in Cardiology|May 7, 2013
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotypeMaren M Limberg, Sven Zumhagen, Michael F Netter, et al.
European Journal of Human Genetics : EJHG|April 2, 2024
A framework for the evaluation and reporting of incidental findings in clinical genomic testingCarolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, et al.
Pageof 4