Author

Samantha Stokes

Dana-Farber Cancer InstituteORCID 0000-0001-8683-9445Unclaimed ORCID profile · follow to get notified of new preprints

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

Frequent Co-Authors

Alexander GuseviD· 1 shared Bruce Evan JohnsoniD· 1 shared Hossein KhiabanianiD· 1 shared Israel GomyiD· 1 shared Judy Ellen GarberiD· 1 shared Laura E. MacConailliD· 1 shared Nahed JallouliD· 1 shared Neal Ian LindemaniD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

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9 top collaborators · 36 mutual co-author links

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1 shared paperBioinformatics

Alexander GusevORCID

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1 paper

Recent·Most cited

BioinformaticsJCO Precision OncologyPeer-reviewedNov 1, 2021

Germline testing data validate inferences of mutational status for variants detected from tumor-only sequencing

Nahed Jalloul, Israel Gomy, Samantha Stokes…·Hossein Khiabanian

This paper evaluates computational methods to infer germline vs. somatic variants from tumor-only sequencing data using 1,608 patients and compares results to germline testing.

17 citations

humanwhole-exome sequencing

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