Author

Eshita Sharma

Centre for Human GeneticsORCID 0000-0002-8663-7365Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David BuckiD· 2 shared Helen E. LockstoneiD· 2 shared Rory J. BowdeniD· 2 shared Alison SimmonsiD· 1 shared Alistair T. PagnamentaiD· 1 shared Anna SchuhiD· 1 shared Claire BryeriD· 1 shared Colin Freeman· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetics

David BuckORCID

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2 papers

Recent·Most cited

GeneticsScientific ReportsPeer-reviewedMar 19, 2021

Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma

Hannah Roberts, Maria Lopopolo, Alistair T. Pagnamenta…·David Buck

This study evaluates the ability of long-read sequencing to detect somatic variants in a lymphoma patient, highlighting the need for specialized tools and the advantages of long reads for structural variants.

23 citations

humanwhole-genome sequencing

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GenomicsScientific ReportsPeer-reviewedJan 26, 2018

A practical solution for preserving single cells for RNA sequencing

Moustafa Attar, Eshita Sharma, Shuqiang Li…·Rory J. Bowden

This paper describes a method using DSP fixation to preserve single cells for RNA sequencing, showing it maintains RNA complexity and reduces technical variability.

80 citations

scRNA-seqexperimental assay

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