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Marcel E Dinger

Showing results (111-120 of 161) with videos related to

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Peerj|August 31, 2017
RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancersVan L T Hoang, Lisa N Tom, Xiu-Cheng Quek, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
Neurology|May 31, 2022
Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisRyan L Davis, Kishore R Kumar, Clare Puttick, et al.
Oncotarget|November 5, 2017
Somatic mutations in salivary duct carcinoma and potential therapeutic targetsTimothy K Khoo, Bing Yu, Joel A Smith, et al.
International Journal of Molecular Sciences|April 12, 2022
Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal DystrophiesBenjamin M Nash, Alan Ma, Gladys Ho, et al.
Scientific Reports|May 27, 2016
The Evx1/Evx1as gene locus regulates anterior-posterior patterning during gastrulationCharles C Bell, Paulo P Amaral, Anton Kalsbeek, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathyAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Genome Biology|May 17, 2023
Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applicationsPatricia J Sullivan, Velimir Gayevskiy, Ryan L Davis, et al.
Nature Methods|March 10, 2015
Quantitative gene profiling of long noncoding RNAs with targeted RNA sequencingMichael B Clark, Tim R Mercer, Giovanni Bussotti, et al.
Cell Reports|October 26, 2017
A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic EncephalopathySushmitha Gururaj, Elizabeth Emma Palmer, Garrett D Sheehan, et al.
Pageof 17

Showing results (111-120 of 161) with videos related to

Sort By:
Pageof 17
Peerj|August 31, 2017
RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancersVan L T Hoang, Lisa N Tom, Xiu-Cheng Quek, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
Neurology|May 31, 2022
Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisRyan L Davis, Kishore R Kumar, Clare Puttick, et al.
Oncotarget|November 5, 2017
Somatic mutations in salivary duct carcinoma and potential therapeutic targetsTimothy K Khoo, Bing Yu, Joel A Smith, et al.
International Journal of Molecular Sciences|April 12, 2022
Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal DystrophiesBenjamin M Nash, Alan Ma, Gladys Ho, et al.
Scientific Reports|May 27, 2016
The Evx1/Evx1as gene locus regulates anterior-posterior patterning during gastrulationCharles C Bell, Paulo P Amaral, Anton Kalsbeek, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathyAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Genome Biology|May 17, 2023
Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applicationsPatricia J Sullivan, Velimir Gayevskiy, Ryan L Davis, et al.
Nature Methods|March 10, 2015
Quantitative gene profiling of long noncoding RNAs with targeted RNA sequencingMichael B Clark, Tim R Mercer, Giovanni Bussotti, et al.
Cell Reports|October 26, 2017
A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic EncephalopathySushmitha Gururaj, Elizabeth Emma Palmer, Garrett D Sheehan, et al.
Pageof 17