Author

Nicole Thomas

Simon Fraser UniversityORCID 0009-0007-9026-2715Unclaimed ORCID profile · follow to get notified of new preprints

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Nicole Thomas2 papers

Biology Disciplines

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Genomics· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Assay:whole-exome sequencing· 3 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Bruno M. GrandeiD· 3 shared Christian SteidliD· 3 shared Christopher K. RushtoniD· 3 shared Prasath PararajalingamiD· 3 shared Ryan D. MoriniD· 3 shared Andrew J. J. MungalliD· 2 shared Barbara MeissneriD· 2 shared David W. ScottiD· 2 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Bruno M. GrandeORCID

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3 papers

Recent·Most cited

BioinformaticsBioinformaticsPeer-reviewedJun 1, 2026

LCR-modules: a collection of workflows for cancer genome analysis

Kostiantyn Dreval, Laura K. Hilton, Bruno M. Grande…·Ryan D. Morin

LCR-modules provides a flexible, automated suite of workflows for cancer genome analysis, supporting diverse sequencing types and enabling reproducible, scalable analysis of over 10,800 samples.

1 citation

whole-exome sequencingwhole-genome sequencing

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GenomicsBloodPeer-reviewedMar 11, 2020

Coding and regulatory drivers of mantle cell lymphoma identified through exome and genome sequencing

Prasath Pararajalingam, Krysta Mila Coyle, Sarah E. Arthur…·Ryan D. Morin

This study identifies genetic drivers of mantle cell lymphoma through exome and genome sequencing, revealing novel mutations in genes involved in RNA splicing and regulation.

71 citationstop 2%

humanwhole-exome sequencing

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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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