Author

Jordi Valls-Margarit

Barcelona Supercomputing CenterORCID 0000-0002-0766-0349Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anna CarrerasiD· 1 shared Beatriz CortésiD· 1 shared Cecilia SalvoroiD· 1 shared Daniel Matías-SáncheziD· 1 shared David TorrentsiD· 1 shared Iván Galván‐FemeníaiD· 1 shared Jon Lerga-JasoiD· 1 shared José Francisco Sánchez-HerreroiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Anna CarrerasORCID

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1 paper

Recent·Most cited

GenomicsNucleic Acids ResearchPeer-reviewedFeb 9, 2022

GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing

Jordi Valls-Margarit, Iván Galván‐Femenía, Daniel Matías-Sánchez…·David Torrents

The paper generates a comprehensive haplotype map of the Iberian population using high-coverage whole-genome sequencing, focusing on structural variants and their imputation capabilities.

14 citations

humanwhole-genome sequencing