Author

Michaël Ryan

ORCID 0000-0003-4585-7174Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Assay:whole-exome sequencing· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Collin J. TokheimiD· 2 shared Kyle Moad· 2 shared Rachel KarchiniD· 2 shared Ben BusbyiD· 1 shared Bradley McIntosh BroomiD· 1 shared Christopher Blair DouvilleiD· 1 shared Christopher WakefieldiD· 1 shared David L. Masica· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersBioinformatics

Collin J. TokheimORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintOct 31, 2020

OmicPioneer-sc: an integrated, interactive visualization environment for single-cell sequencing data

John N. Weinstein, Mary A. Rohrdanz, Mark Stucky…·Bradley McIntosh Broom

OmicPioneer-sc provides an interactive visualization tool for single-cell sequencing data, integrating dimensionality reduction, heat maps, and pathway modules to aid in cell-type annotation and multi-omic analysis.

DOI 10.1101/2020.10.31.363580

humanscRNA-seq

𝕏 PostBluesky

BioinformaticsbioRxivPreprintOct 6, 2019

OpenCRAVAT, an open source collaborative platform for the annotation of human genetic variation

Kymberleigh A. Pagel, Rick Kim, Kyle Moad…·Rachel Karchin

OpenCRAVAT provides an open-source platform for variant and gene prioritization by integrating diverse data resources and computational methods.

7 citations

humanwhole-exome sequencing

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BioinformaticsCancer ResearchPeer-reviewedOct 31, 2017

CRAVAT 4: Cancer-Related Analysis of Variants Toolkit

David L. Masica, Christopher Blair Douville, Collin J. Tokheim…·Rachel Karchin

CRAVAT 4 provides tools for analyzing and interpreting somatic mutations in cancer studies, offering annotation, prioritization, and visualization with a web interface.

74 citations

whole-exome sequencingstatistical model

𝕏 PostBluesky