Author

B. S. Thomas

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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Cancer Biology· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:ATAC-seq· 1 Assay:clinical cohort / trial· 1

Frequent Co-Authors

A. L. Damon· 2 shared C. A. Painter· 2 shared D. Kim· 2 shared E. S. Lander· 2 shared M. Dunphy· 2 shared N. Wagle· 2 shared S. Shah· 2 shared A. Dowdye· 1 shared

Activity by Year

2019-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersCancer Biology

A. L. Damon

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Author profile →

3 papers

Recent·Most cited

A patient-driven clinicogenomic partnership through the Metastatic Prostate Cancer Project

J. Crowdis, S. Balch, L. Sterlin, B. S. Thomas, S. Y. Camp, M. Dunphy, E. Anastasio, S. Shah, A. L. Damon, R. Ramos, D. M. Sosa, I. K. Small, B. Tomson, C. M. Nguyen, M. McGillicuddy, , E. M. Van Allen

The paper describes a patient-driven initiative that collects clinicogenomic data from metastatic prostate cancer patients, revealing consistent patient-reported data and genomic insights from cfDNA samples.

bioRxiv · Jul 9, 2021 · PreprintCancer Biology

The Angiosarcoma Project: enabling genomic and clinical discoveries in a rare cancer through patient-partnered research

C. A. Painter, E. Jain, B. N. Tomson, M. Dunphy, R. E. Stoddard, B. S. Thomas, A. L. Damon, S. Shah, D. Kim, J. Gomez Tejeda Zanudo, J. L. Hornick, Y.-L. Chen, P. Merriam, C. P. Raut, G. D. Demetri, , N. Wagle

The paper describes the Angiosarcoma Project, a patient-partnered initiative that generates genomic data on angiosarcoma, identifying recurrent mutations and potential therapeutic targets.

bioRxiv · Aug 26, 2019Cancer Biology

Transcriptome Dynamics Reveals Progressive Transition from Effector to Memory in CD4+ T cells.

M. S. F. Soon, H. J. Lee, J. A. Engel, J. Straube, B. S. Thomas, L. S. Clarke, P. Laohamonthonkul, C. P. S. Pernold, R. N. Haldar, C. G. Williams, L. I. M. Lansink, R. Koufariotis, V. Lakis, S. Wood, X. Chen, , A. Haque

This study uses single-cell RNA-seq and ATAC-seq to show a progressive transition from effector to memory CD4+ T cells during Plasmodium infection, with linear pathways and memory-associated gene expression.

bioRxiv · Jun 19, 2019 · PreprintImmunology