Author

Víctor García‐Olivares

Consejo Superior de Investigaciones CientíficasORCID 0000-0002-0104-377XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Approach:benchmark study· 2 Research Focus:benchmarking· 2 Organism:human· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1

Frequent Co-Authors

Adrián Muñoz‐BarreraiD· 2 shared Ana Díaz-de UseraiD· 2 shared Antonio Íñigo-CamposiD· 2 shared Carlos FloresiD· 2 shared David JáspeziD· 2 shared Jose Miguel Lorenzo-SalazariD· 2 shared Luis A. Rubio‐RodrígueziD· 2 shared Rafaela González‐MontelongoiD· 2 shared

Activity by Year

2021-2022 · peak 1/yr

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10 top collaborators · 44 mutual co-author links

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2 shared papersGenomics

Adrián Muñoz‐BarreraORCID

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2 papers

Recent·Most cited

A benchmarking of human Y-chromosomal haplogroup classifiers from whole-genome and whole-exome sequence data

Víctor García‐Olivares, Adrián Muñoz‐Barrera, Luis A. Rubio‐Rodríguez, David Jáspez, Ana Díaz-de Usera, Antonio Íñigo-Campos, Krishna R. Veeramah, Santos Alonso, Mark Thomas, Jose Miguel Lorenzo-Salazar, Rafaela González‐Montelongo, Carlos Flores

The paper benchmarks five Y-chromosomal haplogroup classifiers using whole-genome and whole-exome sequencing data, finding YLeaf performs best for both and handles third-generation sequencing data effectively.

bioRxiv · Sep 19, 2022 · PreprintGenomics

A benchmarking of human mitochondrial DNA haplogroup classifiers from whole-genome and whole-exome sequence data

Víctor García‐Olivares, Adrián Muñoz‐Barrera, Jose Miguel Lorenzo-Salazar, Carlos Zaragoza‐Trello, Luis A. Rubio‐Rodríguez, Ana Díaz-de Usera, David Jáspez, Antonio Íñigo-Campos, Rafaela González‐Montelongo, Carlos Flores

This study benchmarks mitochondrial DNA haplogroup classifiers using whole-genome and whole-exome sequencing data, finding Haplocheck as the most accurate tool for short-read data and requiring assembly-based approaches for long-read data.

Scientific Reports · Oct 15, 2021Peer-reviewedGenomics