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Ginger A Metcalf

Showing results (1-10 of 42) with videos related to

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Nature Communications|April 4, 2025
K-mer analysis of long-read alignment pileups for structural variant genotypingAdam C English, Fabio Cunial, Ginger A Metcalf, et al.
Biorxiv : the Preprint Server for Biology|November 1, 2024
K-mer analysis of long-read alignment pileups for structural variant genotypingAdam C English, Fabio Cunial, Ginger A Metcalf, et al.
Genome Biology|December 27, 2022
Truvari: refined structural variant comparison preserves allelic diversityAdam C English, Vipin K Menon, Richard A Gibbs, et al.
JMIR Research Protocols|March 26, 2021
The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care SystemElena Valeryevna Feofanova, Guo-Qiang Zhang, Samden Lhatoo, et al.
Nature Methods|April 30, 2024
Unveiling microbial diversity: harnessing long-read sequencing technologyDaniel P Agustinho, Yilei Fu, Vipin K Menon, et al.
Journal of Clinical Lipidology|February 17, 2026
The impact of genetic testing on physician practice in specialized cardiovascular clinicsArsalan Hamid, Tyler Sewell, Sucheta Bhatt, et al.
Science Advances|September 8, 2016
Loss-of-function variants influence the human serum metabolomeBing Yu, Alexander H Li, Ginger A Metcalf, et al.
Genetics|April 4, 2018
Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic StudyElena V Feofanova, Bing Yu, Ginger A Metcalf, et al.
Genome Biology|November 26, 2016
Whole genome sequence analysis of serum amino acid levelsBing Yu, Paul S de Vries, Ginger A Metcalf, et al.
Human Molecular Genetics|September 1, 2017
Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities studyPaul S de Vries, Bing Yu, Elena V Feofanova, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Nature Communications|April 4, 2025
K-mer analysis of long-read alignment pileups for structural variant genotypingAdam C English, Fabio Cunial, Ginger A Metcalf, et al.
Biorxiv : the Preprint Server for Biology|November 1, 2024
K-mer analysis of long-read alignment pileups for structural variant genotypingAdam C English, Fabio Cunial, Ginger A Metcalf, et al.
Genome Biology|December 27, 2022
Truvari: refined structural variant comparison preserves allelic diversityAdam C English, Vipin K Menon, Richard A Gibbs, et al.
JMIR Research Protocols|March 26, 2021
The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care SystemElena Valeryevna Feofanova, Guo-Qiang Zhang, Samden Lhatoo, et al.
Nature Methods|April 30, 2024
Unveiling microbial diversity: harnessing long-read sequencing technologyDaniel P Agustinho, Yilei Fu, Vipin K Menon, et al.
Journal of Clinical Lipidology|February 17, 2026
The impact of genetic testing on physician practice in specialized cardiovascular clinicsArsalan Hamid, Tyler Sewell, Sucheta Bhatt, et al.
Science Advances|September 8, 2016
Loss-of-function variants influence the human serum metabolomeBing Yu, Alexander H Li, Ginger A Metcalf, et al.
Genetics|April 4, 2018
Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic StudyElena V Feofanova, Bing Yu, Ginger A Metcalf, et al.
Genome Biology|November 26, 2016
Whole genome sequence analysis of serum amino acid levelsBing Yu, Paul S de Vries, Ginger A Metcalf, et al.
Human Molecular Genetics|September 1, 2017
Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities studyPaul S de Vries, Bing Yu, Elena V Feofanova, et al.
Pageof 5