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Mitchell R Vollger

Showing results (1-10 of 49) with videos related to

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Biorxiv : the Preprint Server for Biology|February 27, 2026
<i>rustybam:</i> a composable toolkit for alignment analysis and visualization with <i>SafFire</i>Mitchell R Vollger
Nature Reviews. Genetics|June 7, 2020
Long-read human genome sequencing and its applicationsGlennis A Logsdon, Mitchell R Vollger, Evan E Eichler
Bioinformatics (Oxford, England)|January 12, 2022
StainedGlass: interactive visualization of massive tandem repeat structures with identity heatmapsMitchell R Vollger, Peter Kerpedjiev, Adam M Phillippy, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Epigenetic conditioning improves sequence-based modeling of gene regulation across cell types and allelesOberon Dixon-Luinenburg, Ayesha Bajwa, Mitchell R Vollger, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Integrating Single-Molecule Sequencing and Deep Learning to Predict Haplotype-Specific 3D Chromatin Organization in a Mendelian ConditionDanilo Dubocanin, Anna Kalygina, J Matthew Franklin, et al.
Genome Research|August 18, 2020
HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long readsSergey Nurk, Brian P Walenz, Arang Rhie, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 30, 2019
Human-specific tandem repeat expansion and differential gene expression during primate evolutionArvis Sulovari, Ruiyang Li, Peter A Audano, et al.
Nature Methods|December 19, 2018
Long-read sequence and assembly of segmental duplicationsMitchell R Vollger, Philip C Dishuck, Melanie Sorensen, et al.
Genome Research|May 10, 2023
Gaps and complex structurally variant loci in phased genome assembliesDavid Porubsky, Mitchell R Vollger, William T Harvey, et al.
Genome Research|December 9, 2024
Resolving the chromatin impact of mosaic variants with targeted Fiber-seqStephanie C Bohaczuk, Zachary J Amador, Chang Li, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Biorxiv : the Preprint Server for Biology|February 27, 2026
<i>rustybam:</i> a composable toolkit for alignment analysis and visualization with <i>SafFire</i>Mitchell R Vollger
Nature Reviews. Genetics|June 7, 2020
Long-read human genome sequencing and its applicationsGlennis A Logsdon, Mitchell R Vollger, Evan E Eichler
Bioinformatics (Oxford, England)|January 12, 2022
StainedGlass: interactive visualization of massive tandem repeat structures with identity heatmapsMitchell R Vollger, Peter Kerpedjiev, Adam M Phillippy, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Epigenetic conditioning improves sequence-based modeling of gene regulation across cell types and allelesOberon Dixon-Luinenburg, Ayesha Bajwa, Mitchell R Vollger, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Integrating Single-Molecule Sequencing and Deep Learning to Predict Haplotype-Specific 3D Chromatin Organization in a Mendelian ConditionDanilo Dubocanin, Anna Kalygina, J Matthew Franklin, et al.
Genome Research|August 18, 2020
HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long readsSergey Nurk, Brian P Walenz, Arang Rhie, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 30, 2019
Human-specific tandem repeat expansion and differential gene expression during primate evolutionArvis Sulovari, Ruiyang Li, Peter A Audano, et al.
Nature Methods|December 19, 2018
Long-read sequence and assembly of segmental duplicationsMitchell R Vollger, Philip C Dishuck, Melanie Sorensen, et al.
Genome Research|May 10, 2023
Gaps and complex structurally variant loci in phased genome assembliesDavid Porubsky, Mitchell R Vollger, William T Harvey, et al.
Genome Research|December 9, 2024
Resolving the chromatin impact of mosaic variants with targeted Fiber-seqStephanie C Bohaczuk, Zachary J Amador, Chang Li, et al.
Pageof 5