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David Buck

Showing results (31-40 of 57) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 2, 2013
Whole-exome sequencing studies of nonfunctioning pituitary adenomasPaul J Newey, M Andrew Nesbit, Andrew J Rimmer, et al.
Nature Communications|October 17, 2018
Single cell RNA-seq reveals profound transcriptional similarity between Barrett's oesophagus and oesophageal submucosal glandsRichard Peter Owen, Michael Joseph White, David Tyler Severson, et al.
Plos Computational Biology|August 3, 2021
Using de novo assembly to identify structural variation of eight complex immune system gene regionsJia-Yuan Zhang, Hannah Roberts, David S C Flores, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Nature Communications|April 25, 2019
Sequencing of human genomes with nanopore technologyRory Bowden, Robert W Davies, Andreas Heger, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2013
Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germlineEleni Giannoulatou, Gilean McVean, Indira B Taylor, et al.
BMJ Open|June 8, 2012
A pilot study of rapid benchtop sequencing of Staphylococcus aureus and Clostridium difficile for outbreak detection and surveillanceDavid W Eyre, Tanya Golubchik, N Claire Gordon, et al.
Plos One|June 14, 2013
A modified RNA-Seq approach for whole genome sequencing of RNA viruses from faecal and blood samplesElizabeth M Batty, T H Nicholas Wong, Amy Trebes, et al.
F1000Research|February 3, 2016
MinION Analysis and Reference Consortium: Phase 1 data release and analysisCamilla L C Ip, Matthew Loose, John R Tyson, et al.
HGG Advances|September 11, 2024
Familial severe skeletal Class II malocclusion with gingival hyperplasia caused by a complex structural rearrangement at the KCNJ2-KCNJ16 locusReza Maroofian, Alistair T Pagnamenta, Alireza Navabazam, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
The Journal of Clinical Endocrinology and Metabolism|March 2, 2013
Whole-exome sequencing studies of nonfunctioning pituitary adenomasPaul J Newey, M Andrew Nesbit, Andrew J Rimmer, et al.
Nature Communications|October 17, 2018
Single cell RNA-seq reveals profound transcriptional similarity between Barrett's oesophagus and oesophageal submucosal glandsRichard Peter Owen, Michael Joseph White, David Tyler Severson, et al.
Plos Computational Biology|August 3, 2021
Using de novo assembly to identify structural variation of eight complex immune system gene regionsJia-Yuan Zhang, Hannah Roberts, David S C Flores, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Nature Communications|April 25, 2019
Sequencing of human genomes with nanopore technologyRory Bowden, Robert W Davies, Andreas Heger, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2013
Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germlineEleni Giannoulatou, Gilean McVean, Indira B Taylor, et al.
BMJ Open|June 8, 2012
A pilot study of rapid benchtop sequencing of Staphylococcus aureus and Clostridium difficile for outbreak detection and surveillanceDavid W Eyre, Tanya Golubchik, N Claire Gordon, et al.
Plos One|June 14, 2013
A modified RNA-Seq approach for whole genome sequencing of RNA viruses from faecal and blood samplesElizabeth M Batty, T H Nicholas Wong, Amy Trebes, et al.
F1000Research|February 3, 2016
MinION Analysis and Reference Consortium: Phase 1 data release and analysisCamilla L C Ip, Matthew Loose, John R Tyson, et al.
HGG Advances|September 11, 2024
Familial severe skeletal Class II malocclusion with gingival hyperplasia caused by a complex structural rearrangement at the KCNJ2-KCNJ16 locusReza Maroofian, Alistair T Pagnamenta, Alireza Navabazam, et al.
Pageof 6