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

T Marth

Showing results (101-110 of 104) with videos related to

Pageof 11
Sort By:
You have reached the last page of results.This site can display upto 104 results.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
NPJ Genomic Medicine|March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unitSabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Pageof 11

Showing results (101-110 of 104) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 104 results.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
NPJ Genomic Medicine|March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unitSabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Pageof 11