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

Jay Shendure

Showing results (121-130 of 437) with videos related to

Pageof 44
Sort By:
Nature Methods|April 1, 2010
Single-nucleotide evolutionary constraint scores highlight disease-causing mutationsGregory M Cooper, David L Goode, Sarah B Ng, et al.
Genome Research|November 11, 2016
A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activityFumitaka Inoue, Martin Kircher, Beth Martin, et al.
Genome Research|April 23, 2020
Suppressor mutations in <i>Mecp2</i>-null mice implicate the DNA damage response in Rett syndrome pathologyAdebola Enikanolaiye, Julie Ruston, Rong Zeng, et al.
American Journal of Human Genetics|July 18, 2017
CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic DeletionsMolly Gasperini, Gregory M Findlay, Aaron McKenna, et al.
Nature Communications|May 6, 2017
Quantification of differential gene expression by multiplexed targeted resequencing of cDNAPeer Arts, Jori van der Raadt, Sebastianus H C van Gestel, et al.
Elife|May 25, 2017
The dynamic three-dimensional organization of the diploid yeast genomeSeungsoo Kim, Ivan Liachko, Donna G Brickner, et al.
Nature Reviews. Genetics|September 28, 2011
Exome sequencing as a tool for Mendelian disease gene discoveryMichael J Bamshad, Sarah B Ng, Abigail W Bigham, et al.
Prenatal Diagnosis|April 5, 2013
Noninvasive fetal genome sequencing: a primerMatthew W Snyder, LaVone E Simmons, Jacob O Kitzman, et al.
American Journal of Human Genetics|September 17, 2018
A Multiplex Homology-Directed DNA Repair Assay Reveals the Impact of More Than 1,000 BRCA1 Missense Substitution Variants on Protein FunctionLea M Starita, Muhtadi M Islam, Tapahsama Banerjee, et al.
Nucleic Acids Research|May 6, 2015
Accurate identification of centromere locations in yeast genomes using Hi-CNelle Varoquaux, Ivan Liachko, Ferhat Ay, et al.
Pageof 44

Showing results (121-130 of 437) with videos related to

Sort By:
Pageof 44
Nature Methods|April 1, 2010
Single-nucleotide evolutionary constraint scores highlight disease-causing mutationsGregory M Cooper, David L Goode, Sarah B Ng, et al.
Genome Research|November 11, 2016
A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activityFumitaka Inoue, Martin Kircher, Beth Martin, et al.
Genome Research|April 23, 2020
Suppressor mutations in <i>Mecp2</i>-null mice implicate the DNA damage response in Rett syndrome pathologyAdebola Enikanolaiye, Julie Ruston, Rong Zeng, et al.
American Journal of Human Genetics|July 18, 2017
CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic DeletionsMolly Gasperini, Gregory M Findlay, Aaron McKenna, et al.
Nature Communications|May 6, 2017
Quantification of differential gene expression by multiplexed targeted resequencing of cDNAPeer Arts, Jori van der Raadt, Sebastianus H C van Gestel, et al.
Elife|May 25, 2017
The dynamic three-dimensional organization of the diploid yeast genomeSeungsoo Kim, Ivan Liachko, Donna G Brickner, et al.
Nature Reviews. Genetics|September 28, 2011
Exome sequencing as a tool for Mendelian disease gene discoveryMichael J Bamshad, Sarah B Ng, Abigail W Bigham, et al.
Prenatal Diagnosis|April 5, 2013
Noninvasive fetal genome sequencing: a primerMatthew W Snyder, LaVone E Simmons, Jacob O Kitzman, et al.
American Journal of Human Genetics|September 17, 2018
A Multiplex Homology-Directed DNA Repair Assay Reveals the Impact of More Than 1,000 BRCA1 Missense Substitution Variants on Protein FunctionLea M Starita, Muhtadi M Islam, Tapahsama Banerjee, et al.
Nucleic Acids Research|May 6, 2015
Accurate identification of centromere locations in yeast genomes using Hi-CNelle Varoquaux, Ivan Liachko, Ferhat Ay, et al.
Pageof 44