Author

Tanvi Damle

University of Leeds

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Allysia J. Mak· 1 shared Angela Norie BrooksiD· 1 shared Colette FeltoniD· 1 shared Jon AkutagawaiD· 1 shared Julie L. AspdeniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

5 top collaborators · 10 mutual co-author links

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1 shared paperGenomics

Allysia J. Mak

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1 paper

Recent·Most cited

RNA-sequencing as an expression-informed alternative for somatic variant detection and cancer driver identification

Jon Akutagawa, Allysia J. Mak, Tanvi Damle, Colette Felton, Julie L. Aspden, Angela Norie Brooks

This study uses RNA-seq data to detect somatic variants and identify cancer drivers in 1,359 samples, showing RNA-seq can effectively replace WES/WGS for this task.

bioRxiv · May 10, 2022 · PreprintGenomics