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Manuel Tardaguila

Showing results (1-10 of 14) with videos related to

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Nature Genetics|March 31, 2019
Resolving variant-to-function relationships in hematopoiesisManuel Tardaguila, Nicole Soranzo
G3 (Bethesda, Md.)|July 20, 2018
Event Analysis: Using Transcript Events To Improve Estimates of Abundance in RNA-seq DataJeremy R B Newman, Patrick Concannon, Manuel Tardaguila, et al.
Plos Computational Biology|December 8, 2015
The Characteristics of Heterozygous Protein Truncating Variants in the Human GenomeIstván Bartha, Antonio Rausell, Paul J McLaren, et al.
Nature Genetics|March 15, 2022
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseasesKousik Kundu, Manuel Tardaguila, Alice L Mann, et al.
Human Molecular Genetics|September 22, 2022
GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphologyMichele Marongiu, Gonzalo Pérez-Mejías, Valeria Orrù, et al.
Nature Communications|January 27, 2026
The functional landscape of alternative splicing in hematopoietic lineage commitmentXiao Hu, Jinrui Wang, Li Chen, et al.
Human Molecular Genetics|February 9, 2022
Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traitsBryce Rowland, Sanan Venkatesh, Manuel Tardaguila, et al.
Genome Research|February 15, 2018
SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantificationManuel Tardaguila, Lorena de la Fuente, Cristina Marti, et al.
Genome Research|July 4, 2018
Corrigendum: SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantificationManuel Tardaguila, Lorena de la Fuente, Cristina Marti, et al.
American Journal of Human Genetics|July 25, 2024
Misexpression of inactive genes in whole blood is associated with nearby rare structural variantsThomas Vanderstichele, Katie L Burnham, Niek de Klein, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Nature Genetics|March 31, 2019
Resolving variant-to-function relationships in hematopoiesisManuel Tardaguila, Nicole Soranzo
G3 (Bethesda, Md.)|July 20, 2018
Event Analysis: Using Transcript Events To Improve Estimates of Abundance in RNA-seq DataJeremy R B Newman, Patrick Concannon, Manuel Tardaguila, et al.
Plos Computational Biology|December 8, 2015
The Characteristics of Heterozygous Protein Truncating Variants in the Human GenomeIstván Bartha, Antonio Rausell, Paul J McLaren, et al.
Nature Genetics|March 15, 2022
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseasesKousik Kundu, Manuel Tardaguila, Alice L Mann, et al.
Human Molecular Genetics|September 22, 2022
GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphologyMichele Marongiu, Gonzalo Pérez-Mejías, Valeria Orrù, et al.
Nature Communications|January 27, 2026
The functional landscape of alternative splicing in hematopoietic lineage commitmentXiao Hu, Jinrui Wang, Li Chen, et al.
Human Molecular Genetics|February 9, 2022
Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traitsBryce Rowland, Sanan Venkatesh, Manuel Tardaguila, et al.
Genome Research|February 15, 2018
SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantificationManuel Tardaguila, Lorena de la Fuente, Cristina Marti, et al.
Genome Research|July 4, 2018
Corrigendum: SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantificationManuel Tardaguila, Lorena de la Fuente, Cristina Marti, et al.
American Journal of Human Genetics|July 25, 2024
Misexpression of inactive genes in whole blood is associated with nearby rare structural variantsThomas Vanderstichele, Katie L Burnham, Niek de Klein, et al.
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