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R Quinlan

Showing results (291-300 of 347) with videos related to

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The Journal of Clinical Investigation|October 5, 2013
ACTN3 genotype influences muscle performance through the regulation of calcineurin signalingJane T Seto, Kate G R Quinlan, Monkol Lek, et al.
Biorxiv : the Preprint Server for Biology|July 29, 2024
TRGT-denovo: accurate detection of <i>de novo</i> tandem repeat mutationsT Mokveld, E Dolzhenko, H Dashnow, et al.
Biopreservation and Biobanking|March 18, 2024
Update of the Minimum Information About BIobank Data Sharing (MIABIS) Core Terminology to the 3<sup>rd</sup> VersionNiina Eklund, Cäcilia Engels, Michael Neumann, et al.
Genome Biology|December 14, 2022
STRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel lociHarriet Dashnow, Brent S Pedersen, Laurel Hiatt, 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.
Human Molecular Genetics|May 4, 2011
Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodelingJane T Seto, Monkol Lek, Kate G R Quinlan, et al.
BMC Molecular Biology|June 3, 2014
Differential regulation of the α-globin locus by Krüppel-like Factor 3 in erythroid and non-erythroid cellsAlister P W Funnell, Douglas Vernimmen, Wooi F Lim, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
Genome Biology|February 5, 2015
Extending reference assembly modelsDeanna M Church, Valerie A Schneider, Karyn Meltz Steinberg, et al.
NPJ Genomic Medicine|August 16, 2018
Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathyBetsy E P Ostrander, Russell J Butterfield, Brent S Pedersen, et al.
Pageof 35

Showing results (291-300 of 347) with videos related to

Sort By:
Pageof 35
The Journal of Clinical Investigation|October 5, 2013
ACTN3 genotype influences muscle performance through the regulation of calcineurin signalingJane T Seto, Kate G R Quinlan, Monkol Lek, et al.
Biorxiv : the Preprint Server for Biology|July 29, 2024
TRGT-denovo: accurate detection of <i>de novo</i> tandem repeat mutationsT Mokveld, E Dolzhenko, H Dashnow, et al.
Biopreservation and Biobanking|March 18, 2024
Update of the Minimum Information About BIobank Data Sharing (MIABIS) Core Terminology to the 3<sup>rd</sup> VersionNiina Eklund, Cäcilia Engels, Michael Neumann, et al.
Genome Biology|December 14, 2022
STRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel lociHarriet Dashnow, Brent S Pedersen, Laurel Hiatt, 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.
Human Molecular Genetics|May 4, 2011
Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodelingJane T Seto, Monkol Lek, Kate G R Quinlan, et al.
BMC Molecular Biology|June 3, 2014
Differential regulation of the α-globin locus by Krüppel-like Factor 3 in erythroid and non-erythroid cellsAlister P W Funnell, Douglas Vernimmen, Wooi F Lim, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
Genome Biology|February 5, 2015
Extending reference assembly modelsDeanna M Church, Valerie A Schneider, Karyn Meltz Steinberg, et al.
NPJ Genomic Medicine|August 16, 2018
Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathyBetsy E P Ostrander, Russell J Butterfield, Brent S Pedersen, et al.
Pageof 35