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Nathan C Sheffield

Showing results (51-60 of 65) with videos related to

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Biorxiv : the Preprint Server for Biology|November 24, 2025
Taming the reference genome jungle: the refget sequence collection standardDonald R Campbell, Timothee Cezard, Sveinung Gundersen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2022
Single-cell transcriptome and accessible chromatin dynamics during endocrine pancreas developmentEliza Duvall, Cecil M Benitez, Krissie Tellez, et al.
Genome Biology|October 5, 2012
Chromatin accessibility reveals insights into androgen receptor activation and transcriptional specificityAlok K Tewari, Galip Gürkan Yardimci, Yoichiro Shibata, et al.
Nucleic Acids Research|June 7, 2018
Coloc-stats: a unified web interface to perform colocalization analysis of genomic featuresBoris Simovski, Chakravarthi Kanduri, Sveinung Gundersen, et al.
Plos Genetics|July 5, 2012
Extensive evolutionary changes in regulatory element activity during human origins are associated with altered gene expression and positive selectionYoichiro Shibata, Nathan C Sheffield, Olivier Fedrigo, et al.
Bioinformatics Advances|June 7, 2022
Expanding the Galaxy's reference dataNagampalli VijayKrishna, Jayadev Joshi, Nate Coraor, et al.
Genome Research|July 14, 2011
Open chromatin defined by DNaseI and FAIRE identifies regulatory elements that shape cell-type identityLingyun Song, Zhancheng Zhang, Linda L Grasfeder, et al.
Cell Reports|November 11, 2023
Integrative single-cell meta-analysis reveals disease-relevant vascular cell states and markers in human atherosclerosisJose Verdezoto Mosquera, Gaëlle Auguste, Doris Wong, et al.
Science (New York, N.Y.)|October 27, 2018
The chromatin accessibility landscape of primary human cancersM Ryan Corces, Jeffrey M Granja, Shadi Shams, et al.
Nature Communications|May 29, 2021
Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burdenPeter Peneder, Adrian M Stütz, Didier Surdez, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Biorxiv : the Preprint Server for Biology|November 24, 2025
Taming the reference genome jungle: the refget sequence collection standardDonald R Campbell, Timothee Cezard, Sveinung Gundersen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2022
Single-cell transcriptome and accessible chromatin dynamics during endocrine pancreas developmentEliza Duvall, Cecil M Benitez, Krissie Tellez, et al.
Genome Biology|October 5, 2012
Chromatin accessibility reveals insights into androgen receptor activation and transcriptional specificityAlok K Tewari, Galip Gürkan Yardimci, Yoichiro Shibata, et al.
Nucleic Acids Research|June 7, 2018
Coloc-stats: a unified web interface to perform colocalization analysis of genomic featuresBoris Simovski, Chakravarthi Kanduri, Sveinung Gundersen, et al.
Plos Genetics|July 5, 2012
Extensive evolutionary changes in regulatory element activity during human origins are associated with altered gene expression and positive selectionYoichiro Shibata, Nathan C Sheffield, Olivier Fedrigo, et al.
Bioinformatics Advances|June 7, 2022
Expanding the Galaxy's reference dataNagampalli VijayKrishna, Jayadev Joshi, Nate Coraor, et al.
Genome Research|July 14, 2011
Open chromatin defined by DNaseI and FAIRE identifies regulatory elements that shape cell-type identityLingyun Song, Zhancheng Zhang, Linda L Grasfeder, et al.
Cell Reports|November 11, 2023
Integrative single-cell meta-analysis reveals disease-relevant vascular cell states and markers in human atherosclerosisJose Verdezoto Mosquera, Gaëlle Auguste, Doris Wong, et al.
Science (New York, N.Y.)|October 27, 2018
The chromatin accessibility landscape of primary human cancersM Ryan Corces, Jeffrey M Granja, Shadi Shams, et al.
Nature Communications|May 29, 2021
Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burdenPeter Peneder, Adrian M Stütz, Didier Surdez, et al.
Pageof 7