Author

Dilmi Perera

Memorial Sloan Kettering Cancer Center

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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Biochemistry· 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:deep learning· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Aaron Agarunov· 1 shared Ahmet ZehiriD· 1 shared Aijazuddin SyediD· 1 shared Alan LiiD· 1 shared Aliaksandra Samoila· 1 shared Angela Rose BrannoniD· 1 shared Anita S. BowmaniD· 1 shared Anoop Balakrishnan RemaiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenomics

Aaron Agarunov

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2 papers

Recent·Most cited

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, Juber Patel, Разумова Анна Ивановна, Yu Hu, Fanli Meng, Mohammad Haque, Justyna Sadowska, Brian J. Murphy, Tessara Baldi, Ian Johnson, Ryan N. Ptashkin, Maysun Hasan, Preethi Srinivasan, , 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.

bioRxiv · Jun 27, 2020 · PreprintGenomics

In search of non-coding driver mutations by deep sequencing of regulatory elements in colorectal cancer

Rebecca C Poulos, Dilmi Perera, Deborah Packham, Anushi Shah, Caroline Janitz, John E Pimanda, Nicholas Hawkins, Robyn L Ward, Luke B Hesson, Jason WH Wong

This study uses targeted capture sequencing to identify non-coding driver mutations in colorectal cancer, finding no clear driver variants in a cohort of 95 samples.

bioRxiv · Jan 16, 2018 · PreprintBiochemistry