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

Vincent C T Hanlon

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

Pageof 1
Sort By:
Nature Genetics|March 26, 2026
Strand-seq and the future of personalized genomicsVincent C T Hanlon, Peter M Lansdorp
Methods in Molecular Biology (Clifton, N.J.)|November 6, 2022
Chromosome-Length Haplotypes with StrandPhaseR and Strand-seqVincent C T Hanlon, David Porubsky, Peter M Lansdorp
Human Mutation|September 1, 2022
A survey of current methods to detect and genotype inversionsVincent C T Hanlon, Peter M Lansdorp, Victor Guryev
Evolution Letters|August 8, 2019
Somatic mutations substantially increase the per-generation mutation rate in the conifer <i>Picea sitchensis</i>Vincent C T Hanlon, Sarah P Otto, Sally N Aitken
Nature Genetics|June 27, 2025
How and when organisms edit their own genomesVincent C T Hanlon, Alex Cagan, Sebastian Eves-van den Akker
BMC Genomics|August 1, 2021
InvertypeR: Bayesian inversion genotyping with Strand-seq dataVincent C T Hanlon, Carl-Adam Mattsson, Diana C J Spierings, et al.
Cell Genomics|February 13, 2023
Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seqVahid Akbari, Vincent C T Hanlon, Kieran O'Neill, et al.
Cell Reports Methods|April 27, 2022
Construction of Strand-seq libraries in open nanoliter arraysVincent C T Hanlon, Daniel D Chan, Zeid Hamadeh, et al.
Nature|April 24, 2025
Human de novo mutation rates from a four-generation pedigree referenceDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human <i>de novo</i> mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Pageof 1

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

Sort By:
Pageof 1
Nature Genetics|March 26, 2026
Strand-seq and the future of personalized genomicsVincent C T Hanlon, Peter M Lansdorp
Methods in Molecular Biology (Clifton, N.J.)|November 6, 2022
Chromosome-Length Haplotypes with StrandPhaseR and Strand-seqVincent C T Hanlon, David Porubsky, Peter M Lansdorp
Human Mutation|September 1, 2022
A survey of current methods to detect and genotype inversionsVincent C T Hanlon, Peter M Lansdorp, Victor Guryev
Evolution Letters|August 8, 2019
Somatic mutations substantially increase the per-generation mutation rate in the conifer <i>Picea sitchensis</i>Vincent C T Hanlon, Sarah P Otto, Sally N Aitken
Nature Genetics|June 27, 2025
How and when organisms edit their own genomesVincent C T Hanlon, Alex Cagan, Sebastian Eves-van den Akker
BMC Genomics|August 1, 2021
InvertypeR: Bayesian inversion genotyping with Strand-seq dataVincent C T Hanlon, Carl-Adam Mattsson, Diana C J Spierings, et al.
Cell Genomics|February 13, 2023
Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seqVahid Akbari, Vincent C T Hanlon, Kieran O'Neill, et al.
Cell Reports Methods|April 27, 2022
Construction of Strand-seq libraries in open nanoliter arraysVincent C T Hanlon, Daniel D Chan, Zeid Hamadeh, et al.
Nature|April 24, 2025
Human de novo mutation rates from a four-generation pedigree referenceDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human <i>de novo</i> mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Pageof 1