Author

Samantha J.L. Knight

National Institute for Health and Care ResearchORCID 0000-0002-6047-3462Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Anna SchuhiD· 2 shared Helene Marie-Pierre DreauiD· 2 shared Jenny C. TayloriD· 2 shared Alistair T. PagnamentaiD· 1 shared Basile StamatopoulosiD· 1 shared Colin Freeman· 1 shared David BuckiD· 1 shared Davide RossiiD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

Anna SchuhORCID

Mutual co-authors in cluster

Author profile →

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

𝕏 PostBluesky

GenomicsHemaSpherePeer-reviewedJun 1, 2019

Differential genomic and transcriptomic events associated with high-grade transformation of Chronic Lymphocytic Leukemia

Jenny Klintman, Basile Stamatopoulos, Kate E. Ridout…·Anna Schuh

The paper identifies genomic and transcriptomic changes in CLL transforming to RS, finding pathway mutations and non-coding mutations in PAX5 enhancers associated with transformation.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky