Author

Krysta Mila Coyle

Simon Fraser UniversityORCID 0000-0002-1309-4873Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Bruno M. GrandeiD· 2 shared Christian SteidliD· 2 shared Christopher K. RushtoniD· 2 shared Nicole ThomasiD· 2 shared Prasath PararajalingamiD· 2 shared Ryan D. MoriniD· 2 shared Andrew J. J. MungalliD· 1 shared Barbara MeissneriD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersBioinformatics

Bruno M. GrandeORCID

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2 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

𝕏 PostBluesky

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

𝕏 PostBluesky