Author

Khédoudja Nafa

Memorial Sloan Kettering Cancer CenterORCID 0000-0002-7467-6682Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Ahmet ZehiriD· 2 shared Angela Rose BrannoniD· 2 shared Anita S. BowmaniD· 2 shared Chad VanderbiltiD· 2 shared Gowtham JayakumaraniD· 2 shared Ivelise RijoiD· 2 shared Jamal K. BenhamidaiD· 2 shared JinJuan YaoiD· 2 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Ahmet ZehirORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 3, 2022

Enhanced clinical assessment of hematologic malignancies through routine paired tumor:normal sequencing

Ryan N. Ptashkin, Mark David Ewalt, Gowtham Jayakumaran…·Maria E. Arcila

This study presents a paired tumor:normal sequencing dataset for hematologic malignancies, showing improved identification of somatic variants and their clinical relevance.

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintJun 27, 2020

Enhanced specificity of high sensitivity somatic variant profiling in cell-free DNA via paired normal sequencing: design, validation, and clinical experience of the MSK-ACCESS liquid biopsy assay

Angela Rose Brannon, Gowtham Jayakumaran, Monica S. Diosdado…·Ryma Benayed

The paper describes the development and clinical application of MSK-ACCESS, a liquid biopsy assay that improves the specificity of somatic variant detection in cell-free DNA by using paired normal sequencing.

7 citations

humanwhole-exome sequencing

𝕏 PostBluesky