Author

D. Starenki

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

Biology Disciplines

Click to filter author papers

Immunology· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:bulk RNA-seq· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

A. Forero· 1 shared A. LoBuglio· 1 shared D. Buchsbaum· 1 shared H. Koch· 1 shared M. Li· 1 shared Q. Li· 1 shared R. Arend· 1 shared R. M. Myers· 1 shared

Activity by Year

2018-2018 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperImmunology

A. Forero

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

ImmunologybioRxivOct 22, 2018

powerTCR: a model-based approach to comparative analysis of the clone size distribution of the T cell receptor repertoire

H. Koch, D. Starenki, S. J. Cooper…·Q. Li

The paper introduces a model-based method to analyze T cell receptor repertoire clone size distributions and applies it to datasets to identify differences across biological conditions.

DOI 10.1371/journal.pcbi.1006571

humanbulk RNA-seq

𝕏 PostBluesky

ImmunologybioRxivApr 3, 2018

The expression of class II major histocompatibility molecules on breast tumors delays T cell exhaustion, expands the T cell repertoire and slows tumor growth

T. McCaw, M. Li, D. Starenki…·T. Randall

This study shows that MHCII expression on breast tumors slows growth, recruits more T cells, expands TCR diversity, and delays exhaustion, but does not prevent exhaustion.

DOI 10.1007/s00262-018-2262-5

mousebulk RNA-seq

𝕏 PostBluesky