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Perry G Ridge

Showing results (31-40 of 65) with videos related to

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Plos One|September 17, 2013
Mitochondrial haplotypes associated with biomarkers for Alzheimer's diseasePerry G Ridge, Andre Koop, Taylor J Maxwell, et al.
Gigabyte (Hong Kong, China)|March 27, 2023
Genome assembly of the roundjaw bonefish (<i>Albula glossodonta</i>), a vulnerable circumtropical sportfishBrandon D Pickett, Sheena Talma, Jessica R Glass, et al.
BMC Genomics|July 1, 2016
Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levelsMark T W Ebbert, Lyndsay A Staley, Joshua Parker, et al.
Genome Medicine|May 30, 2012
Consensus: a framework for evaluation of uncertain gene variants in laboratory test reportingDavid K Crockett, Perry G Ridge, Andrew R Wilson, et al.
BMC Plant Biology|June 8, 2019
Arabidopsis thaliana organelles mimic the T7 phage DNA replisome with specific interactions between Twinkle protein and DNA polymerases Pol1A and Pol1BStewart A Morley, Antolín Peralta-Castro, Luis G Brieba, et al.
NAR Genomics and Bioinformatics|June 6, 2022
The Ramp Atlas: facilitating tissue and cell-specific ramp sequence analyses through an intuitive web interfaceJustin B Miller, Taylor E Meurs, Matthew W Hodgman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 10, 2015
Interaction between variants in CLU and MS4A4E modulates Alzheimer's disease riskMark T W Ebbert, Kevin L Boehme, Mark E Wadsworth, et al.
BMC Bioinformatics|July 26, 2016
Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approachesMark T W Ebbert, Mark E Wadsworth, Lyndsay A Staley, et al.
BMC Bioinformatics|August 1, 2014
Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) filesMark T W Ebbert, Mark E Wadsworth, Kevin L Boehme, et al.
BMC Medical Genomics|November 15, 2012
A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspectiveWhitney L Wooderchak-Donahue, Brendan O'Fallon, Larissa V Furtado, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Plos One|September 17, 2013
Mitochondrial haplotypes associated with biomarkers for Alzheimer's diseasePerry G Ridge, Andre Koop, Taylor J Maxwell, et al.
Gigabyte (Hong Kong, China)|March 27, 2023
Genome assembly of the roundjaw bonefish (<i>Albula glossodonta</i>), a vulnerable circumtropical sportfishBrandon D Pickett, Sheena Talma, Jessica R Glass, et al.
BMC Genomics|July 1, 2016
Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levelsMark T W Ebbert, Lyndsay A Staley, Joshua Parker, et al.
Genome Medicine|May 30, 2012
Consensus: a framework for evaluation of uncertain gene variants in laboratory test reportingDavid K Crockett, Perry G Ridge, Andrew R Wilson, et al.
BMC Plant Biology|June 8, 2019
Arabidopsis thaliana organelles mimic the T7 phage DNA replisome with specific interactions between Twinkle protein and DNA polymerases Pol1A and Pol1BStewart A Morley, Antolín Peralta-Castro, Luis G Brieba, et al.
NAR Genomics and Bioinformatics|June 6, 2022
The Ramp Atlas: facilitating tissue and cell-specific ramp sequence analyses through an intuitive web interfaceJustin B Miller, Taylor E Meurs, Matthew W Hodgman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 10, 2015
Interaction between variants in CLU and MS4A4E modulates Alzheimer's disease riskMark T W Ebbert, Kevin L Boehme, Mark E Wadsworth, et al.
BMC Bioinformatics|July 26, 2016
Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approachesMark T W Ebbert, Mark E Wadsworth, Lyndsay A Staley, et al.
BMC Bioinformatics|August 1, 2014
Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) filesMark T W Ebbert, Mark E Wadsworth, Kevin L Boehme, et al.
BMC Medical Genomics|November 15, 2012
A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspectiveWhitney L Wooderchak-Donahue, Brendan O'Fallon, Larissa V Furtado, et al.
Pageof 7