Author

Efren Sandoval

Primary ORCID profile (0000-0003-1314-3927 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Efren SandovaliD1 paper · Helix (United States)

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:database / resource· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ahmed Moustafa· 1 shared Amalio TelentiiD· 1 shared Brad A Perkins· 1 shared Chad Garner· 1 shared Chao XieiD· 1 shared Emily H.M. Wong· 1 shared Ewen F Kirkness· 1 shared Franz J Och· 1 shared

Activity by Year

2016-2016 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Ahmed Moustafa

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1 paper

Recent·Most cited

Deep Sequencing of 10,000 Human Genomes

Amalio Telenti, Levi T Pierce, William H Biggs, Julia di Iulio, Emily H.M. Wong, Martin M Fabani, Ewen F Kirkness, Ahmed Moustafa, Naisha Shah, Chao Xie, Suzanne C Brewerton, Nadeem Bulsara, Chad Garner, Gary Metzker, Efren Sandoval, , J. Craig Venter

This study sequences 10,545 human genomes at 30-40x coverage, identifying 150 million variants and showing 84% of the genome can be confidently sequenced, with implications for clinical use.

Proceedings of the National Academy of Sciences · Oct 4, 2016Peer-reviewedGenomics