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Matt Velinder

Showing results (1-10 of 12) with videos related to

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BMC Bioinformatics|December 10, 2020
ped_draw: pedigree drawing with easeMatt Velinder, Dillon Lee, Gabor Marth
BMC Medical Genomics|December 13, 2019
Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene listsAditya Ekawade, Matt Velinder, Alistair Ward, 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.
Neurology. Genetics|April 14, 2023
<i>SON</i>-Related Zhu-Tokita-Takenouchi-Kim Syndrome With Recurrent Hemiplegic Migraine: Putative Role of <i>PRRT2</i>Jordan Langford, Lana Vukadin, John C Carey, et al.
Journal of Clinical and Translational Science|May 1, 2018
Rapid clinical diagnostic variant investigation of genomic patient sequencing data with <i>iobio</i> web toolsAlistair Ward, Mary A Karren, Tonya Di Sera, et al.
NPJ Genomic Medicine|July 16, 2021
Effective variant filtering and expected candidate variant yield in studies of rare human diseaseBrent S Pedersen, Joe M Brown, Harriet Dashnow, et al.
Scientific Reports|April 7, 2022
Author Correction: Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritizationTonya Di Sera, Matt Velinder, Alistair Ward, et al.
Scientific Reports|October 14, 2021
Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritizationTonya Di Sera, Matt Velinder, Alistair Ward, et al.
Journal of Medical Genetics|September 24, 2018
Genome sequencing reveals a deep intronic splicing <i>ACVRL1</i> mutation hotspot in Hereditary Haemorrhagic TelangiectasiaWhitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, et al.
Medrxiv : the Preprint Server for Health Sciences|November 11, 2020
gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritizationTonya Di Sera, Matt Velinder, Alistair Ward, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
BMC Bioinformatics|December 10, 2020
ped_draw: pedigree drawing with easeMatt Velinder, Dillon Lee, Gabor Marth
BMC Medical Genomics|December 13, 2019
Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene listsAditya Ekawade, Matt Velinder, Alistair Ward, 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.
Neurology. Genetics|April 14, 2023
<i>SON</i>-Related Zhu-Tokita-Takenouchi-Kim Syndrome With Recurrent Hemiplegic Migraine: Putative Role of <i>PRRT2</i>Jordan Langford, Lana Vukadin, John C Carey, et al.
Journal of Clinical and Translational Science|May 1, 2018
Rapid clinical diagnostic variant investigation of genomic patient sequencing data with <i>iobio</i> web toolsAlistair Ward, Mary A Karren, Tonya Di Sera, et al.
NPJ Genomic Medicine|July 16, 2021
Effective variant filtering and expected candidate variant yield in studies of rare human diseaseBrent S Pedersen, Joe M Brown, Harriet Dashnow, et al.
Scientific Reports|April 7, 2022
Author Correction: Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritizationTonya Di Sera, Matt Velinder, Alistair Ward, et al.
Scientific Reports|October 14, 2021
Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritizationTonya Di Sera, Matt Velinder, Alistair Ward, et al.
Journal of Medical Genetics|September 24, 2018
Genome sequencing reveals a deep intronic splicing <i>ACVRL1</i> mutation hotspot in Hereditary Haemorrhagic TelangiectasiaWhitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, et al.
Medrxiv : the Preprint Server for Health Sciences|November 11, 2020
gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritizationTonya Di Sera, Matt Velinder, Alistair Ward, et al.
Pageof 2