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

Andrew Carroll

Showing results (31-40 of 118) with videos related to

Pageof 12
Sort By:
Plos One|March 24, 2022
Depth and benthic habitat influence shallow and mesophotic predatory fishes on a remote, high-latitude coral reefKristy Brown, Jacquomo Monk, Joel Williams, et al.
Macromolecular Bioscience|January 14, 2017
Tough, Semisynthetic Hydrogels for Adipose Derived Stem Cell Delivery for Chondral Defect RepairFraz Anjum, Andrew Carroll, Stuart A Young, et al.
Early Intervention in Psychiatry|July 3, 2019
Victimization, violence and facial affect recognition in a community sample of first-episode psychosis patientsHenning Hachtel, Rachael Fullam, Aisling Malone, et al.
BMC Genomics|June 13, 2026
Two Australian genome assemblies expand the genomic blueprint of giant kelpHugo J Scharfenstein, Andrew Carroll, Jakop Schwoerbel, et al.
Plos One|June 26, 2015
Inexpensive and Highly Reproducible Cloud-Based Variant Calling of 2,535 Human GenomesSuyash S Shringarpure, Andrew Carroll, Francisco M De La Vega, et al.
BMC Bioinformatics|May 12, 2023
Improving variant calling using population data and deep learningNae-Chyun Chen, Alexey Kolesnikov, Sidharth Goel, et al.
Biochemical and Biophysical Research Communications|April 17, 2010
Raman imaging of cell wall polymers in Arabidopsis thalianaMartin Schmidt, Adam M Schwartzberg, Andrew Carroll, et al.
Bioinformatics (Oxford, England)|January 5, 2021
Accurate, scalable cohort variant calls using DeepVariant and GLnexusTaedong Yun, Helen Li, Pi-Chuan Chang, et al.
BMC Bioinformatics|September 11, 2016
A hybrid computational strategy to address WGS variant analysis in >5000 samplesZhuoyi Huang, Navin Rustagi, Narayanan Veeraraghavan, et al.
Genome Research|April 28, 2022
A complete pedigree-based graph workflow for rare candidate variant analysisCharles Markello, Charles Huang, Alex Rodriguez, et al.
Pageof 12

Showing results (31-40 of 118) with videos related to

Sort By:
Pageof 12
Plos One|March 24, 2022
Depth and benthic habitat influence shallow and mesophotic predatory fishes on a remote, high-latitude coral reefKristy Brown, Jacquomo Monk, Joel Williams, et al.
Macromolecular Bioscience|January 14, 2017
Tough, Semisynthetic Hydrogels for Adipose Derived Stem Cell Delivery for Chondral Defect RepairFraz Anjum, Andrew Carroll, Stuart A Young, et al.
Early Intervention in Psychiatry|July 3, 2019
Victimization, violence and facial affect recognition in a community sample of first-episode psychosis patientsHenning Hachtel, Rachael Fullam, Aisling Malone, et al.
BMC Genomics|June 13, 2026
Two Australian genome assemblies expand the genomic blueprint of giant kelpHugo J Scharfenstein, Andrew Carroll, Jakop Schwoerbel, et al.
Plos One|June 26, 2015
Inexpensive and Highly Reproducible Cloud-Based Variant Calling of 2,535 Human GenomesSuyash S Shringarpure, Andrew Carroll, Francisco M De La Vega, et al.
BMC Bioinformatics|May 12, 2023
Improving variant calling using population data and deep learningNae-Chyun Chen, Alexey Kolesnikov, Sidharth Goel, et al.
Biochemical and Biophysical Research Communications|April 17, 2010
Raman imaging of cell wall polymers in Arabidopsis thalianaMartin Schmidt, Adam M Schwartzberg, Andrew Carroll, et al.
Bioinformatics (Oxford, England)|January 5, 2021
Accurate, scalable cohort variant calls using DeepVariant and GLnexusTaedong Yun, Helen Li, Pi-Chuan Chang, et al.
BMC Bioinformatics|September 11, 2016
A hybrid computational strategy to address WGS variant analysis in >5000 samplesZhuoyi Huang, Navin Rustagi, Narayanan Veeraraghavan, et al.
Genome Research|April 28, 2022
A complete pedigree-based graph workflow for rare candidate variant analysisCharles Markello, Charles Huang, Alex Rodriguez, et al.
Pageof 12