Author

Valentin V. Barsan

Stanford MedicineORCID 0000-0001-5099-9009Unclaimed 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 Assay:whole-genome sequencing· 1

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Ana Granat· 1 shared Drew Kennedy· 1 shared Erich B. JaegeriD· 1 shared Feng CheniD· 1 shared Irina Khrebtukova· 1 shared Jessica P. HamptoniD· 1 shared M. Kyle CromeriD· 1 shared Matthew Hebden PorteusiD· 1 shared

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2021-2021 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Ana Granat

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintOct 27, 2021

Ultra-deep sequencing reveals no evidence of oncogenic mutations or enrichment by ex vivo CRISPR/Cas9 genome editing in human hematopoietic stem and progenitor cells

M. Kyle Cromer, Valentin V. Barsan, Erich B. Jaeger…·Matthew Hebden Porteus

The paper uses ultra-deep sequencing to assess oncogenic mutations in human hematopoietic stem and progenitor cells after CRISPR/Cas9 editing, finding no evidence of tumorigenic variants.

DOI 10.1101/2021.10.27.466166

humanwhole-genome sequencing

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