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Jesper Eisfeldt

Showing results (1-10 of 68) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
Hybrid Sequencing Characterization of Complex Chromosomal RearrangementsAnna Lindstrand, Jesper Eisfeldt
Bioinformatics (Oxford, England)|November 19, 2024
Detecting transposable elements in long-read genomes using sTELLeRKristine Bilgrav Saether, Jesper Eisfeldt
BMC Bioinformatics|April 5, 2020
pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencingJessada Thutkawkorapin, Jesper Eisfeldt, Emma Tham, et al.
Nature Genetics|May 7, 2025
Toward clinical long-read genome sequencing for rare diseasesJesper Eisfeldt, Marlene Ek, Magnus Nordenskjöld, et al.
Nature Biotechnology|January 6, 2026
Moving beyond monogenic disorders in clinical healthcareAnders Kämpe, Oda Blomqvist Picard, Jesper Eisfeldt, et al.
F1000Research|August 9, 2017
<i>TIDDIT</i>, an efficient and comprehensive structural variant caller for massive parallel sequencing dataJesper Eisfeldt, Francesco Vezzi, Pall Olason, et al.
Plos One|March 27, 2018
AMYCNE: Confident copy number assessment using whole genome sequencing dataJesper Eisfeldt, Daniel Nilsson, Johanna C Andersson-Assarsson, et al.
Molecular Biology and Evolution|September 28, 2019
Discovery of Novel Sequences in 1,000 Swedish GenomesJesper Eisfeldt, Gustaf Mårtensson, Adam Ameur, et al.
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
Scientific Reports|November 9, 2021
A database on differentially expressed microRNAs during rodent bladder healingClara Ibel Chamorro, Jesper Eisfeldt, Oliver Willacy, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
Hybrid Sequencing Characterization of Complex Chromosomal RearrangementsAnna Lindstrand, Jesper Eisfeldt
Bioinformatics (Oxford, England)|November 19, 2024
Detecting transposable elements in long-read genomes using sTELLeRKristine Bilgrav Saether, Jesper Eisfeldt
BMC Bioinformatics|April 5, 2020
pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencingJessada Thutkawkorapin, Jesper Eisfeldt, Emma Tham, et al.
Nature Genetics|May 7, 2025
Toward clinical long-read genome sequencing for rare diseasesJesper Eisfeldt, Marlene Ek, Magnus Nordenskjöld, et al.
Nature Biotechnology|January 6, 2026
Moving beyond monogenic disorders in clinical healthcareAnders Kämpe, Oda Blomqvist Picard, Jesper Eisfeldt, et al.
F1000Research|August 9, 2017
<i>TIDDIT</i>, an efficient and comprehensive structural variant caller for massive parallel sequencing dataJesper Eisfeldt, Francesco Vezzi, Pall Olason, et al.
Plos One|March 27, 2018
AMYCNE: Confident copy number assessment using whole genome sequencing dataJesper Eisfeldt, Daniel Nilsson, Johanna C Andersson-Assarsson, et al.
Molecular Biology and Evolution|September 28, 2019
Discovery of Novel Sequences in 1,000 Swedish GenomesJesper Eisfeldt, Gustaf Mårtensson, Adam Ameur, et al.
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
Scientific Reports|November 9, 2021
A database on differentially expressed microRNAs during rodent bladder healingClara Ibel Chamorro, Jesper Eisfeldt, Oliver Willacy, et al.
Pageof 7