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

Nigel P Carter

Showing results (81-90 of 104) with videos related to

Pageof 11
Sort By:
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Genome Research|June 26, 2008
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs)Vardhman K Rakyan, Thomas A Down, Natalie P Thorne, et al.
American Journal of Human Genetics|January 29, 2013
Genetic basis of Y-linked hearing impairmentQiuju Wang, Yali Xue, Yujun Zhang, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Plos One|April 19, 2013
Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndromeSusan M Gribble, Frances K Wiseman, Stephen Clayton, et al.
Genome Research|June 15, 2007
The landscape of histone modifications across 1% of the human genome in five human cell linesChristoph M Koch, Robert M Andrews, Paul Flicek, et al.
Genome Research|November 24, 2006
Accurate and reliable high-throughput detection of copy number variation in the human genomeHeike Fiegler, Richard Redon, Dan Andrews, et al.
Science (New York, N.Y.)|September 29, 2007
Paired-end mapping reveals extensive structural variation in the human genomeJan O Korbel, Alexander Eckehart Urban, Jason P Affourtit, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Nature Genetics|April 6, 2010
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencingHansoo Park, Jong-Il Kim, Young Seok Ju, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Genome Research|June 26, 2008
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs)Vardhman K Rakyan, Thomas A Down, Natalie P Thorne, et al.
American Journal of Human Genetics|January 29, 2013
Genetic basis of Y-linked hearing impairmentQiuju Wang, Yali Xue, Yujun Zhang, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Plos One|April 19, 2013
Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndromeSusan M Gribble, Frances K Wiseman, Stephen Clayton, et al.
Genome Research|June 15, 2007
The landscape of histone modifications across 1% of the human genome in five human cell linesChristoph M Koch, Robert M Andrews, Paul Flicek, et al.
Genome Research|November 24, 2006
Accurate and reliable high-throughput detection of copy number variation in the human genomeHeike Fiegler, Richard Redon, Dan Andrews, et al.
Science (New York, N.Y.)|September 29, 2007
Paired-end mapping reveals extensive structural variation in the human genomeJan O Korbel, Alexander Eckehart Urban, Jason P Affourtit, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Nature Genetics|April 6, 2010
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencingHansoo Park, Jong-Il Kim, Young Seok Ju, et al.
Pageof 11