Author

Martin M Fabani

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Genomics· 1

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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

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

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2016-2016 · peak 1/yr

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1 shared paperGenomics

Ahmed Moustafa

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1 paper

Recent·Most cited

GenomicsProceedings of the National Academy of SciencesPeer-reviewedOct 4, 2016

Deep Sequencing of 10,000 Human Genomes

Amalio Telenti, Levi T Pierce, William H Biggs…·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.

DOI 10.1073/pnas.1613365113

humanwhole-genome sequencing

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