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Methods in Molecular Biology (Clifton, N.J.)
|
August 30, 2025
Hybrid Sequencing Characterization of Complex Chromosomal Rearrangements
Anna Lindstrand, Jesper Eisfeldt
Bioinformatics (Oxford, England)
|
November 19, 2024
Detecting transposable elements in long-read genomes using sTELLeR
Kristine 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 sequencing
Jessada Thutkawkorapin, Jesper Eisfeldt, Emma Tham, et al.
Nature Genetics
|
May 7, 2025
Toward clinical long-read genome sequencing for rare diseases
Jesper Eisfeldt, Marlene Ek, Magnus Nordenskjöld, et al.
Nature Biotechnology
|
January 6, 2026
Moving beyond monogenic disorders in clinical healthcare
Anders 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 data
Jesper Eisfeldt, Francesco Vezzi, Pall Olason, et al.
Plos One
|
March 27, 2018
AMYCNE: Confident copy number assessment using whole genome sequencing data
Jesper Eisfeldt, Daniel Nilsson, Johanna C Andersson-Assarsson, et al.
Molecular Biology and Evolution
|
September 28, 2019
Discovery of Novel Sequences in 1,000 Swedish Genomes
Jesper Eisfeldt, Gustaf Mårtensson, Adam Ameur, et al.
Frontiers in Genetics
|
June 16, 2023
Discovery of non-reference processed pseudogenes in the Swedish population
Esmee Ten Berk de Boer, Kristine Bilgrav Saether, Jesper Eisfeldt
Scientific Reports
|
November 9, 2021
A database on differentially expressed microRNAs during rodent bladder healing
Clara Ibel Chamorro, Jesper Eisfeldt, Oliver Willacy, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
Methods in Molecular Biology (Clifton, N.J.)
|
August 30, 2025
Hybrid Sequencing Characterization of Complex Chromosomal Rearrangements
Anna Lindstrand, Jesper Eisfeldt
Bioinformatics (Oxford, England)
|
November 19, 2024
Detecting transposable elements in long-read genomes using sTELLeR
Kristine 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 sequencing
Jessada Thutkawkorapin, Jesper Eisfeldt, Emma Tham, et al.
Nature Genetics
|
May 7, 2025
Toward clinical long-read genome sequencing for rare diseases
Jesper Eisfeldt, Marlene Ek, Magnus Nordenskjöld, et al.
Nature Biotechnology
|
January 6, 2026
Moving beyond monogenic disorders in clinical healthcare
Anders 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 data
Jesper Eisfeldt, Francesco Vezzi, Pall Olason, et al.
Plos One
|
March 27, 2018
AMYCNE: Confident copy number assessment using whole genome sequencing data
Jesper Eisfeldt, Daniel Nilsson, Johanna C Andersson-Assarsson, et al.
Molecular Biology and Evolution
|
September 28, 2019
Discovery of Novel Sequences in 1,000 Swedish Genomes
Jesper Eisfeldt, Gustaf Mårtensson, Adam Ameur, et al.
Frontiers in Genetics
|
June 16, 2023
Discovery of non-reference processed pseudogenes in the Swedish population
Esmee Ten Berk de Boer, Kristine Bilgrav Saether, Jesper Eisfeldt
Scientific Reports
|
November 9, 2021
A database on differentially expressed microRNAs during rodent bladder healing
Clara Ibel Chamorro, Jesper Eisfeldt, Oliver Willacy, et al.
Page
of 7