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David Jáspez

Showing results (1-10 of 16) with videos related to

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Nucleic Acids Research|October 26, 2018
liqDB: a small-RNAseq knowledge discovery database for liquid biopsy studiesErnesto Aparicio-Puerta, David Jáspez, Ricardo Lebrón, et al.
Life (Basel, Switzerland)|November 26, 2022
From Samples to Germline and Somatic Sequence Variation: A Focus on Next-Generation Sequencing in Melanoma ResearchAdrián Muñoz-Barrera, Luis A Rubio-Rodríguez, Ana Díaz-de Usera, et al.
Computational and Structural Biotechnology Journal|July 24, 2025
Benchmarking of bioinformatics tools for the hybrid <i>de novo</i> assembly of human and non-human whole-genome sequencing dataAdrián Muñoz-Barrera, Luis A Rubio-Rodríguez, David Jáspez, et al.
Scientific Reports|October 16, 2021
A benchmarking of human mitochondrial DNA haplogroup classifiers from whole-genome and whole-exome sequence dataVíctor García-Olivares, Adrián Muñoz-Barrera, José M Lorenzo-Salazar, et al.
Computational and Structural Biotechnology Journal|October 11, 2023
Benchmarking of human Y-chromosomal haplogroup classifiers with whole-genome and whole-exome sequence dataVíctor García-Olivares, Adrián Muñoz-Barrera, Luis A Rubio-Rodríguez, et al.
Scientific Reports|September 28, 2022
Developing CIRdb as a catalog of natural genetic variation in the Canary IslandersAna Díaz-de Usera, Luis A Rubio-Rodríguez, Adrián Muñoz-Barrera, et al.
Iscience|January 17, 2023
Digging into the admixture strata of current-day Canary Islanders based on mitogenomesVíctor García-Olivares, Luis A Rubio-Rodríguez, Adrián Muñoz-Barrera, et al.
European Journal of Human Genetics : EJHG|January 3, 2025
A tiered strategy to identify relevant genetic variants in familial pulmonary fibrosis: a proof of concept for the clinical practiceAitana Alonso-González, Ibrahim Véliz-Flores, Eva Tosco-Herrera, et al.
Human Mutation|September 2, 2022
Evaluation of a whole-exome sequencing pipeline and benchmarking of causal germline variant prioritizersEva Tosco-Herrera, Adrián Muñoz-Barrera, David Jáspez, et al.
The Lancet. Respiratory Medicine|May 1, 2025
Rare variants and survival of patients with idiopathic pulmonary fibrosis: analysis of a multicentre, observational cohort study with independent validationAitana Alonso-González, David Jáspez, José M Lorenzo-Salazar, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|October 26, 2018
liqDB: a small-RNAseq knowledge discovery database for liquid biopsy studiesErnesto Aparicio-Puerta, David Jáspez, Ricardo Lebrón, et al.
Life (Basel, Switzerland)|November 26, 2022
From Samples to Germline and Somatic Sequence Variation: A Focus on Next-Generation Sequencing in Melanoma ResearchAdrián Muñoz-Barrera, Luis A Rubio-Rodríguez, Ana Díaz-de Usera, et al.
Computational and Structural Biotechnology Journal|July 24, 2025
Benchmarking of bioinformatics tools for the hybrid <i>de novo</i> assembly of human and non-human whole-genome sequencing dataAdrián Muñoz-Barrera, Luis A Rubio-Rodríguez, David Jáspez, et al.
Scientific Reports|October 16, 2021
A benchmarking of human mitochondrial DNA haplogroup classifiers from whole-genome and whole-exome sequence dataVíctor García-Olivares, Adrián Muñoz-Barrera, José M Lorenzo-Salazar, et al.
Computational and Structural Biotechnology Journal|October 11, 2023
Benchmarking of human Y-chromosomal haplogroup classifiers with whole-genome and whole-exome sequence dataVíctor García-Olivares, Adrián Muñoz-Barrera, Luis A Rubio-Rodríguez, et al.
Scientific Reports|September 28, 2022
Developing CIRdb as a catalog of natural genetic variation in the Canary IslandersAna Díaz-de Usera, Luis A Rubio-Rodríguez, Adrián Muñoz-Barrera, et al.
Iscience|January 17, 2023
Digging into the admixture strata of current-day Canary Islanders based on mitogenomesVíctor García-Olivares, Luis A Rubio-Rodríguez, Adrián Muñoz-Barrera, et al.
European Journal of Human Genetics : EJHG|January 3, 2025
A tiered strategy to identify relevant genetic variants in familial pulmonary fibrosis: a proof of concept for the clinical practiceAitana Alonso-González, Ibrahim Véliz-Flores, Eva Tosco-Herrera, et al.
Human Mutation|September 2, 2022
Evaluation of a whole-exome sequencing pipeline and benchmarking of causal germline variant prioritizersEva Tosco-Herrera, Adrián Muñoz-Barrera, David Jáspez, et al.
The Lancet. Respiratory Medicine|May 1, 2025
Rare variants and survival of patients with idiopathic pulmonary fibrosis: analysis of a multicentre, observational cohort study with independent validationAitana Alonso-González, David Jáspez, José M Lorenzo-Salazar, et al.
Pageof 2