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Barry Moore

Showing results (31-40 of 62) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Phenotype-first patient matching with SimPheny identifies diagnostic candidates beyond curated gene associationsIsabelle B Cooperstein, Alistair Ward, Shilpa N Kobren, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 23, 2016
Large-Scale Synthesis of Helicene-Like Molecules for the Design of Enantiopure Thin Films with Strong Chiroptical ActivityAmina Bensalah-Ledoux, Delphine Pitrat, Thibault Reynaldo, et al.
Current Protocols in Human Genetics|April 26, 2014
Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing DataBrett Kennedy, Zev Kronenberg, Hao Hu, et al.
American Journal of Obstetrics and Gynecology|March 6, 2014
Pharmacogenomics of 17-alpha hydroxyprogesterone caproate for recurrent preterm birth preventionTracy A Manuck, W Scott Watkins, Barry Moore, et al.
Journal of Personalized Medicine|January 21, 2022
<i>Clin.iobio</i>: A Collaborative Diagnostic Workflow to Enable Team-Based Precision GenomicsAlistair Ward, Matt Velinder, Tonya Di Sera, et al.
Genome Research|November 21, 2007
MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomesBrandi L Cantarel, Ian Korf, Sofia M C Robb, et al.
Genome Biology|August 28, 2010
A standard variation file format for human genome sequencesMartin G Reese, Barry Moore, Colin Batchelor, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 25, 2014
Acid/base-triggered switching of circularly polarized luminescence and electronic circular dichroism in organic and organometallic helicenesNidal Saleh, Barry Moore, Monika Srebro, et al.
BMC Bioinformatics|February 22, 2018
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization toolSteven Flygare, Edgar Javier Hernandez, Lon Phan, et al.
HGG Advances|December 2, 2020
Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic herniasEric L Bogenschutz, Zac D Fox, Andrew Farrell, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Phenotype-first patient matching with SimPheny identifies diagnostic candidates beyond curated gene associationsIsabelle B Cooperstein, Alistair Ward, Shilpa N Kobren, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 23, 2016
Large-Scale Synthesis of Helicene-Like Molecules for the Design of Enantiopure Thin Films with Strong Chiroptical ActivityAmina Bensalah-Ledoux, Delphine Pitrat, Thibault Reynaldo, et al.
Current Protocols in Human Genetics|April 26, 2014
Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing DataBrett Kennedy, Zev Kronenberg, Hao Hu, et al.
American Journal of Obstetrics and Gynecology|March 6, 2014
Pharmacogenomics of 17-alpha hydroxyprogesterone caproate for recurrent preterm birth preventionTracy A Manuck, W Scott Watkins, Barry Moore, et al.
Journal of Personalized Medicine|January 21, 2022
<i>Clin.iobio</i>: A Collaborative Diagnostic Workflow to Enable Team-Based Precision GenomicsAlistair Ward, Matt Velinder, Tonya Di Sera, et al.
Genome Research|November 21, 2007
MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomesBrandi L Cantarel, Ian Korf, Sofia M C Robb, et al.
Genome Biology|August 28, 2010
A standard variation file format for human genome sequencesMartin G Reese, Barry Moore, Colin Batchelor, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 25, 2014
Acid/base-triggered switching of circularly polarized luminescence and electronic circular dichroism in organic and organometallic helicenesNidal Saleh, Barry Moore, Monika Srebro, et al.
BMC Bioinformatics|February 22, 2018
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization toolSteven Flygare, Edgar Javier Hernandez, Lon Phan, et al.
HGG Advances|December 2, 2020
Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic herniasEric L Bogenschutz, Zac D Fox, Andrew Farrell, et al.
Pageof 7