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Laurent Francioli

Showing results (1-10 of 9) with videos related to

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Photochemistry and Photobiology|January 13, 2011
A numeric model to simulate solar individual ultraviolet exposureDavid Vernez, Antoine Milon, Laurent Francioli, et al.
Bioinformatics (Oxford, England)|September 1, 2018
novoCaller: a Bayesian network approach for de novo variant calling from pedigree and population sequence dataAnwoy Kumar Mohanty, Dana Vuzman, Laurent Francioli, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 13, 2017
Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated lociSamuel Lessard, Laurent Francioli, Jessica Alfoldi, et al.
Bioinformatics (Oxford, England)|May 16, 2019
Variant Score Ranker-a web application for intuitive missense variant prioritizationJuanjiangmeng Du, Monica Sudarsanam, Eduardo Pérez-Palma, et al.
Human Mutation|October 30, 2019
Recurrent TTN metatranscript-only c.39974-11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathySamantha J Bryen, Lisa J Ewans, Jason Pinner, et al.
Nature Medicine|May 29, 2020
The effect of LRRK2 loss-of-function variants in humansNicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Nature Medicine|January 23, 2021
Author Correction: The effect of LRRK2 loss-of-function variants in humansNicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Photochemistry and Photobiology|January 13, 2011
A numeric model to simulate solar individual ultraviolet exposureDavid Vernez, Antoine Milon, Laurent Francioli, et al.
Bioinformatics (Oxford, England)|September 1, 2018
novoCaller: a Bayesian network approach for de novo variant calling from pedigree and population sequence dataAnwoy Kumar Mohanty, Dana Vuzman, Laurent Francioli, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 13, 2017
Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated lociSamuel Lessard, Laurent Francioli, Jessica Alfoldi, et al.
Bioinformatics (Oxford, England)|May 16, 2019
Variant Score Ranker-a web application for intuitive missense variant prioritizationJuanjiangmeng Du, Monica Sudarsanam, Eduardo Pérez-Palma, et al.
Human Mutation|October 30, 2019
Recurrent TTN metatranscript-only c.39974-11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathySamantha J Bryen, Lisa J Ewans, Jason Pinner, et al.
Nature Medicine|May 29, 2020
The effect of LRRK2 loss-of-function variants in humansNicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Nature Medicine|January 23, 2021
Author Correction: The effect of LRRK2 loss-of-function variants in humansNicola Whiffin, Irina M Armean, Aaron Kleinman, et al.
Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 1