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Benedict Paten

Showing results (91-100 of 203) with videos related to

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Genes|January 20, 2021
Real-Time Culture-Independent Microbial Profiling Onboard the International Space Station Using Nanopore SequencingSarah Stahl-Rommel, Miten Jain, Hang N Nguyen, et al.
Alzheimer'S & Dementia (New York, N. Y.)|August 24, 2023
Bridging the rodent to human translational gap: Marmosets as model systems for the study of Alzheimer's diseaseStacey J Sukoff Rizzo, Gregg Homanics, David J Schaeffer, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2026
Origin and evolution of acrocentric chromosomes in human and great apesSteven J Solar, Prajna Hebbar, Leonardo Gomes de Lima, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 2024
A region of suppressed recombination misleads neoavian phylogenomicsSiavash Mirarab, Iker Rivas-González, Shaohong Feng, et al.
Nature|May 10, 2023
Increased mutation and gene conversion within human segmental duplicationsMitchell R Vollger, Philip C Dishuck, William T Harvey, et al.
Medrxiv : the Preprint Server for Health Sciences|February 24, 2025
Long-read sequencing resolves the clinically relevant <i>CYP21A2</i> locus, supporting a new clinical test for Congenital Adrenal HyperplasiaJean Monlong, Xiao Chen, Hayk Barseghyan, et al.
Journal of the American Medical Informatics Association : JAMIA|July 16, 2015
The NIH BD2K center for big data in translational genomicsBenedict Paten, Mark Diekhans, Brian J Druker, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
G3 (Bethesda, Md.)|April 19, 2019
The Genome of C57BL/6J "Eve", the Mother of the Laboratory Mouse Genome Reference StrainVishal Kumar Sarsani, Narayanan Raghupathy, Ian T Fiddes, et al.
Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Pageof 21

Showing results (91-100 of 203) with videos related to

Sort By:
Pageof 21
Genes|January 20, 2021
Real-Time Culture-Independent Microbial Profiling Onboard the International Space Station Using Nanopore SequencingSarah Stahl-Rommel, Miten Jain, Hang N Nguyen, et al.
Alzheimer'S & Dementia (New York, N. Y.)|August 24, 2023
Bridging the rodent to human translational gap: Marmosets as model systems for the study of Alzheimer's diseaseStacey J Sukoff Rizzo, Gregg Homanics, David J Schaeffer, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2026
Origin and evolution of acrocentric chromosomes in human and great apesSteven J Solar, Prajna Hebbar, Leonardo Gomes de Lima, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 2024
A region of suppressed recombination misleads neoavian phylogenomicsSiavash Mirarab, Iker Rivas-González, Shaohong Feng, et al.
Nature|May 10, 2023
Increased mutation and gene conversion within human segmental duplicationsMitchell R Vollger, Philip C Dishuck, William T Harvey, et al.
Medrxiv : the Preprint Server for Health Sciences|February 24, 2025
Long-read sequencing resolves the clinically relevant <i>CYP21A2</i> locus, supporting a new clinical test for Congenital Adrenal HyperplasiaJean Monlong, Xiao Chen, Hayk Barseghyan, et al.
Journal of the American Medical Informatics Association : JAMIA|July 16, 2015
The NIH BD2K center for big data in translational genomicsBenedict Paten, Mark Diekhans, Brian J Druker, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
G3 (Bethesda, Md.)|April 19, 2019
The Genome of C57BL/6J "Eve", the Mother of the Laboratory Mouse Genome Reference StrainVishal Kumar Sarsani, Narayanan Raghupathy, Ian T Fiddes, et al.
Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Pageof 21