Author

Lauren C. Chong

Ontario Institute for Cancer ResearchORCID 0009-0007-8613-602XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:human· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Assay:scRNA-seq· 1 Research Focus:software / tool· 1 Research Focus:spatial domain detection· 1 Research Focus:trajectory inference· 1

Frequent Co-Authors

Anja MottokiD· 2 shared Christian SteidliD· 2 shared Daniel LaiiD· 2 shared Sohrab P. ShahiD· 2 shared Aileen LuiD· 1 shared Aixiang JiangiD· 1 shared Allen W. ZhangiD· 1 shared Amanda Murdoch· 1 shared

Activity by Year

2018-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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2 shared papersBioinformatics

Anja MottokORCID

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3 papers

Recent·Most cited

BioinformaticsBMC BioinformaticsPeer-reviewedJan 21, 2019

BPG: Seamless, Automated and Interactive Visualization of Scientific Data

Christine P’ng, Jeffrey J. Green, Lauren C. Chong…·Paul Christopher Boutros

BPG is an R package that generates publication-quality, customizable plots and offers an interactive web tool for figure customization and integration with computational pipelines.

117 citationstop 3%

statistical modelsoftware / tool

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BioinformaticsbioRxivPreprintJan 16, 2019

Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers

Allen W. Zhang, Ciara H. O’Flanagan, Elizabeth A. Chavez…·Sohrab P. Shah

CellAssign probabilistically assigns cell types to scRNA-seq data, revealing spatiotemporal dynamics in human cancers like ovarian and follicular lymphoma.

9 citations

humanscRNA-seq

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GenomicsNature CommunicationsPeer-reviewedSep 25, 2018

Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma

Sarah E. Arthur, Aixiang Jiang, Bruno M. Grande…·Ryan D. Morin

This study identifies somatic coding and regulatory variants in DLBCL, revealing novel mechanisms of oncogene deregulation and potential therapeutic targets.

146 citationstop 1%

humanwhole-exome sequencing

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