Author

M. Hugaboom

Harvard UniversityORCID 0000-0001-8099-3564Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

M. Hugaboom1 paper

Biology Disciplines

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Cancer Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Organism:human· 2 Assay:scRNA-seq· 2 Research Focus:clustering· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1

Frequent Co-Authors

David A. BrauniD· 2 shared A. Bacchiocchi· 1 shared A. CalderaiD· 1 shared A. Elliot· 1 shared A. Frey· 1 shared A. KodaiD· 1 shared A. NaqashiD· 1 shared A. VanderwaldeiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersImmunology

David A. BraunORCID

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2 papers

Recent·Most cited

ImmunologybioRxivPreprintFeb 20, 2026

VDJdive and ECLIPSE enhance single-cell TCR sequencing analysis through the probabilistic resolution of ambiguous clonotypes

Ethan C Burns, Mercedeh Javanbakht Movassagh, Jill F. Lundell…·David A. Braun

VDJdive and ECLIPSE resolve ambiguous clonotypes in scTCR-seq by improving chain pairing and clone size estimation, enhancing clonal tracking across conditions.

DOI 10.64898/2026.02.18.706444

𝕏 PostBluesky

Cancer BiologybioRxivPreprintDec 12, 2025

Perturbational single-cell profiling of patient tumors defines lineage- and context-specific programs of innate immune resistance

C. Perry, A. Frey, Y. Fei…·J.J. Ishizuka

The paper uses patient tumor samples to identify lineage- and context-specific mechanisms of innate immune resistance through perturbational single-cell RNA sequencing.

DOI 10.64898/2025.12.09.693245

𝕏 PostBluesky