Author

Gilad Mishne

Color (United States)ORCID 0009-0009-6858-0228Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 1 Research Focus:polygenic risk· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

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Alicia Yiran ZhouiD· 1 shared Amit V. KheraiD· 1 shared Cynthia L. NebeniD· 1 shared Julian R. HomburgeriD· 1 shared Sekar KathiresaniD· 1 shared

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2019-2019 · peak 1/yr

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Alicia Yiran ZhouORCID

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1 paper

Recent·Most cited

GenomicsGenome MedicinePeer-reviewedNov 26, 2019

Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores

Julian R. Homburger, Cynthia L. Neben, Gilad Mishne…·Amit V. Khera

This study shows low coverage whole genome sequencing can accurately assess common variants and calculate polygenic scores, comparable to genotyping arrays.

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humanwhole-genome sequencing

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