Author

Anna S. Nam

Weill Cornell MedicineORCID 0000-0003-4192-8916Unclaimed ORCID profile · follow to get notified of new preprints

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Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Hower LeeiD· 1 shared Kellie WiseiD· 1 shared Luciano Gastón MartelottoiD· 1 shared Marco GrilloiD· 1 shared Martha Holdar· 1 shared Mats F. NilssoniD· 1 shared Michael J. RoachiD· 1 shared Mirca Saras Saurty-SeerungheniD· 1 shared

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2026-2026 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperMolecular Biology

Hower LeeORCID

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1 paper

Recent·Most cited

Molecular BiologybioRxivPreprintApr 12, 2026

Targeted sequencing of mutations via RNA-templated gap filling of oligonucleotides for single-cell RNA-seq

Mirca Saras Saurty-Seerunghen, Hower Lee, Martha Holdar…·Marco Grillo

This paper introduces a method for targeted sequencing of expressed mutations in single cells using RNA-templated gap filling with BstFL polymerase, enabling simultaneous transcriptomic and mutation profiling.

DOI 10.64898/2026.04.10.717677

scRNA-seqexperimental assay

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