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Jean Monlong

Showing results (31-40 of 43) with videos related to

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Cell Reports|March 22, 2024
Evolution of chromosome-arm aberrations in breast cancer through genetic network rewiringElena Kuzmin, Toby M Baker, Tom Lesluyes, et al.
Nature Biotechnology|March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencingSneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Nature Biotechnology|July 21, 2020
Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomesKishwar Shafin, Trevor Pesout, Ryan Lorig-Roach, et al.
Genome Research|November 23, 2013
Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemiaPedro G Ferreira, Pedro Jares, Daniel Rico, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 21, 2020
A Preclinical Trial and Molecularly Annotated Patient Cohort Identify Predictive Biomarkers in Homologous Recombination-deficient Pancreatic CancerYifan Wang, Jin Yong Patrick Park, Alain Pacis, et al.
F1000Research|August 16, 2021
A strategy for building and using a human reference pangenomeBastien Llamas, Giuseppe Narzisi, Valerie Schneider, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
Long-read sequencing of hundreds of diverse brains provides insight into the impact of structural variation on gene expression and DNA methylationKimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.
Nature Genetics|November 27, 2019
Stalled developmental programs at the root of pediatric brain tumorsSelin Jessa, Alexis Blanchet-Cohen, Brian Krug, et al.
Nature Genetics|February 7, 2020
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotranspositionBernardo Rodriguez-Martin, Eva G Alvarez, Adrian Baez-Ortega, et al.
Nature|September 17, 2013
Transcriptome and genome sequencing uncovers functional variation in humansTuuli Lappalainen, Michael Sammeth, Marc R Friedländer, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Cell Reports|March 22, 2024
Evolution of chromosome-arm aberrations in breast cancer through genetic network rewiringElena Kuzmin, Toby M Baker, Tom Lesluyes, et al.
Nature Biotechnology|March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencingSneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Nature Biotechnology|July 21, 2020
Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomesKishwar Shafin, Trevor Pesout, Ryan Lorig-Roach, et al.
Genome Research|November 23, 2013
Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemiaPedro G Ferreira, Pedro Jares, Daniel Rico, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 21, 2020
A Preclinical Trial and Molecularly Annotated Patient Cohort Identify Predictive Biomarkers in Homologous Recombination-deficient Pancreatic CancerYifan Wang, Jin Yong Patrick Park, Alain Pacis, et al.
F1000Research|August 16, 2021
A strategy for building and using a human reference pangenomeBastien Llamas, Giuseppe Narzisi, Valerie Schneider, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
Long-read sequencing of hundreds of diverse brains provides insight into the impact of structural variation on gene expression and DNA methylationKimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.
Nature Genetics|November 27, 2019
Stalled developmental programs at the root of pediatric brain tumorsSelin Jessa, Alexis Blanchet-Cohen, Brian Krug, et al.
Nature Genetics|February 7, 2020
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotranspositionBernardo Rodriguez-Martin, Eva G Alvarez, Adrian Baez-Ortega, et al.
Nature|September 17, 2013
Transcriptome and genome sequencing uncovers functional variation in humansTuuli Lappalainen, Michael Sammeth, Marc R Friedländer, et al.
Pageof 5