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

Wolfram Höps

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
F1000Research|May 4, 2018
Gene Unprediction with Spurio: A tool to identify spurious protein sequencesWolfram Höps, Matt Jeffryes, Alex Bateman
Nature Communications|September 12, 2024
Impact and characterization of serial structural variations across humans and great apesWolfram Höps, Tobias Rausch, Michael Jendrusch, et al.
Genome Biology|April 30, 2023
Inversion polymorphism in a complete human genome assemblyDavid Porubsky, William T Harvey, Allison N Rozanski, et al.
Nature Genetics|June 17, 2020
Recurrent inversion toggling and great ape genome evolutionDavid Porubsky, Ashley D Sanders, Wolfram Höps, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Distinct mechanisms of CNV formation at the human 15q13.3 locusWolfram Höps, David Porubsky, DongAhn Yoo, et al.
American Journal of Human Genetics|January 14, 2025
HiFi long-read genomes for difficult-to-detect, clinically relevant variantsWolfram Höps, Marjan M Weiss, Ronny Derks, et al.
Cell|May 7, 2022
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disordersDavid Porubsky, Wolfram Höps, Hufsah Ashraf, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Break-induced replication underlies formation of inverted triplications and generates unexpected diversity in haplotype structuresChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
Cell Genomics|June 22, 2024
Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder lociChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
Nature|July 23, 2025
Structural variation in 1,019 diverse humans based on long-read sequencingSiegfried Schloissnig, Samarendra Pani, Jana Ebler, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
F1000Research|May 4, 2018
Gene Unprediction with Spurio: A tool to identify spurious protein sequencesWolfram Höps, Matt Jeffryes, Alex Bateman
Nature Communications|September 12, 2024
Impact and characterization of serial structural variations across humans and great apesWolfram Höps, Tobias Rausch, Michael Jendrusch, et al.
Genome Biology|April 30, 2023
Inversion polymorphism in a complete human genome assemblyDavid Porubsky, William T Harvey, Allison N Rozanski, et al.
Nature Genetics|June 17, 2020
Recurrent inversion toggling and great ape genome evolutionDavid Porubsky, Ashley D Sanders, Wolfram Höps, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Distinct mechanisms of CNV formation at the human 15q13.3 locusWolfram Höps, David Porubsky, DongAhn Yoo, et al.
American Journal of Human Genetics|January 14, 2025
HiFi long-read genomes for difficult-to-detect, clinically relevant variantsWolfram Höps, Marjan M Weiss, Ronny Derks, et al.
Cell|May 7, 2022
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disordersDavid Porubsky, Wolfram Höps, Hufsah Ashraf, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Break-induced replication underlies formation of inverted triplications and generates unexpected diversity in haplotype structuresChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
Cell Genomics|June 22, 2024
Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder lociChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
Nature|July 23, 2025
Structural variation in 1,019 diverse humans based on long-read sequencingSiegfried Schloissnig, Samarendra Pani, Jana Ebler, et al.
Pageof 2