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Aaron R Quinlan

Showing results (81-90 of 104) with videos related to

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Scientific Reports|June 21, 2020
Germline mutation rates in young adults predict longevity and reproductive lifespanRichard M Cawthon, Huong D Meeks, Thomas A Sasani, 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.
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.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Human acrocentric chromosome short arm <i>de novo</i> mutation and recombinationJiadong Lin, F Kumara Mastrorosa, Michelle D Noyes, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
A family portrait of the genomic factors shaping tandem repeat mutagenesisThomas A Sasani, Michael E Goldberg, Akshay K Avvaru, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2025
A genome-wide approach for the discovery of novel repeat expansion disorders in the Undiagnosed Diseases Network cohortSarah Fazal, Harriet Dashnow, Maike F Dohrn, et al.
Nature Methods|January 22, 2008
Whole-genome sequencing and variant discovery in C. elegansLaDeana W Hillier, Gabor T Marth, Aaron R Quinlan, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
Scientific Reports|June 21, 2020
Germline mutation rates in young adults predict longevity and reproductive lifespanRichard M Cawthon, Huong D Meeks, Thomas A Sasani, 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.
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.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Human acrocentric chromosome short arm <i>de novo</i> mutation and recombinationJiadong Lin, F Kumara Mastrorosa, Michelle D Noyes, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
A family portrait of the genomic factors shaping tandem repeat mutagenesisThomas A Sasani, Michael E Goldberg, Akshay K Avvaru, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2025
A genome-wide approach for the discovery of novel repeat expansion disorders in the Undiagnosed Diseases Network cohortSarah Fazal, Harriet Dashnow, Maike F Dohrn, et al.
Nature Methods|January 22, 2008
Whole-genome sequencing and variant discovery in C. elegansLaDeana W Hillier, Gabor T Marth, Aaron R Quinlan, et al.
Pageof 11