Author

Jessilyn Dunn

Stanford MedicineORCID 0000-0002-3241-8183Unclaimed 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 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Colleen M. CraigiD· 1 shared Denis N. SalinsiD· 1 shared Elizabeth Colbert· 1 shared Hannes Luc RöstiD· 1 shared Jessica Wheeler· 1 shared Jonathan Adam BernsteiniD· 1 shared Lars Michael SteinmetziD· 1 shared M. Reza SailaniiD· 1 shared

Activity by Year

2017-2017 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Colleen M. CraigORCID

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1 paper

Recent·Most cited

GenomicsbioRxivPreprintJun 18, 2017

High Frequency Actionable Pathogenic Exome Mutations in an Average-Risk Cohort

Shannon M. Rego, Orit Dagan‐Rosenfeld, Wenyu Zhou…·Michael P. Snyder

The paper assesses exome sequencing in a healthy cohort to determine the frequency of medically actionable and non-actionable findings, finding 17% had actionable variants, including some outside standard guidelines.

5 citations

humanwhole-exome sequencing

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