Author

Sharmili Roy

Stanford MedicineORCID 0009-0005-9340-901XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Billy T. LauiD· 2 shared Hanlee P. JiiD· 2 shared Alison Figueroa AlmedaiD· 1 shared Anuja SatheiD· 1 shared Carlos I. Ayala· 1 shared Heon Seok KimiD· 1 shared Kedar TatwawadiiD· 1 shared Mary K. WoottersiD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersSynthetic Biology

Billy T. LauORCID

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2 papers

Recent·Most cited

Synthetic BiologyScientific ReportsPeer-reviewedMay 25, 2023

Magnetic DNA random access memory with nanopore readouts and exponentially-scaled combinatorial addressing

Billy T. Lau, Shubham Chandak, Sharmili Roy…·Hanlee P. Ji

This paper introduces MDRAM, a DNA-based random access memory system that enables efficient and scalable readouts using nanopore sequencing and magnetic bead conjugation.

22 citations

DNA methylationwhole-genome sequencing

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GenomicsbioRxivPreprintNov 22, 2022

Adaptive nanopore sequencing for single cell characterization of cancer mutations and gene rearrangements

Susan M. Grimes, Heon Seok Kim, Sharmili Roy…·Hanlee P. Ji

This study develops a single-cell method using nanopore sequencing to identify somatic mutations and gene rearrangements in cancer cells and integrates these with transcriptomes.

1 citation

humanlong-read sequencing

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