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Kristine Bilgrav Saether

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Bioinformatics (Oxford, England)|November 19, 2024
Detecting transposable elements in long-read genomes using sTELLeRKristine Bilgrav Saether, Jesper Eisfeldt
Frontiers in Genetics|June 16, 2023
Discovery of non-reference processed pseudogenes in the Swedish populationEsmee Ten Berk de Boer, Kristine Bilgrav Saether, Jesper Eisfeldt
Plos One|July 28, 2023
Transposable element insertions in 1000 Swedish individualsKristine Bilgrav Saether, Daniel Nilsson, Håkan Thonberg, et al.
Genome Research|March 25, 2026
Centromeric instability and chromoanasynthesis observed in nine supernumerary marker chromosomes resolved with long-read genome sequencingKristine Bilgrav Saether, Angelo Salazar Mantero, Marlene Ek, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversionsKristine Bilgrav Saether, Jesper Eisfeldt, Jesse Bengtsson, et al.
Genome Research|November 1, 2024
Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gapsKristine Bilgrav Saether, Jesper Eisfeldt, Jesse D Bengtsson, et al.
Molecular Oncology|March 20, 2024
Combining VPS34 inhibitors with STING agonists enhances type I interferon signaling and anti-tumor efficacyYasmin Yu, Madhumita Bogdan, Muhammad Zaeem Noman, et al.
Genome Research|October 29, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexitiesJesper Eisfeldt, Adam Ameur, Felix Lenner, et al.
Genome Medicine|October 17, 2025
Recommendations for bioinformatics in clinical practiceKsenia Lavrichenko, Emilie Sofie Engdal, Rasmus L Marvig, et al.
Nature Genetics|October 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed HackathonAngelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan, et al.
Pageof 1

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

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|November 19, 2024
Detecting transposable elements in long-read genomes using sTELLeRKristine Bilgrav Saether, Jesper Eisfeldt
Frontiers in Genetics|June 16, 2023
Discovery of non-reference processed pseudogenes in the Swedish populationEsmee Ten Berk de Boer, Kristine Bilgrav Saether, Jesper Eisfeldt
Plos One|July 28, 2023
Transposable element insertions in 1000 Swedish individualsKristine Bilgrav Saether, Daniel Nilsson, Håkan Thonberg, et al.
Genome Research|March 25, 2026
Centromeric instability and chromoanasynthesis observed in nine supernumerary marker chromosomes resolved with long-read genome sequencingKristine Bilgrav Saether, Angelo Salazar Mantero, Marlene Ek, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversionsKristine Bilgrav Saether, Jesper Eisfeldt, Jesse Bengtsson, et al.
Genome Research|November 1, 2024
Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gapsKristine Bilgrav Saether, Jesper Eisfeldt, Jesse D Bengtsson, et al.
Molecular Oncology|March 20, 2024
Combining VPS34 inhibitors with STING agonists enhances type I interferon signaling and anti-tumor efficacyYasmin Yu, Madhumita Bogdan, Muhammad Zaeem Noman, et al.
Genome Research|October 29, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexitiesJesper Eisfeldt, Adam Ameur, Felix Lenner, et al.
Genome Medicine|October 17, 2025
Recommendations for bioinformatics in clinical practiceKsenia Lavrichenko, Emilie Sofie Engdal, Rasmus L Marvig, et al.
Nature Genetics|October 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed HackathonAngelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan, et al.
Pageof 1