Author

Sean DeLong

York UniversityORCID 0000-0003-0342-7862Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:database / resource· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Kirsten M. FarncombeiD· 2 shared Raymond H. KimiD· 2 shared Adam C. CoffmaniD· 1 shared Aleksandar MilosavljevićiD· 1 shared Alex Handler WagneriD· 1 shared Alexander R. MarriD· 1 shared Andreea ChioreaniD· 1 shared Arpad M. DanosiD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersBioinformatics

Kirsten M. FarncombeORCID

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2 papers

Recent·Most cited

BioinformaticsBMC Medical GenomicsPeer-reviewedFeb 18, 2022

GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation

Roozbeh Manshaei, Sean DeLong, Veronica Andric…·S. Mohsen Hosseini

GeneTerpret streamlines genomic variant interpretation by integrating multiple data sources and ACMG criteria to prioritize potentially causal variants for a given genome and phenotype.

3 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky

GenomicsbioRxivPreprintJun 13, 2021

Evolution of the open-access CIViC knowledgebase is driven by the needsof the cancer variant interpretation community

Kilannin Krysiak, Arpad M. Danos, Susanna Kiwala…·Malachi Griffith

The paper describes the evolution of the CIViC knowledgebase to meet the needs of the cancer variant interpretation community by expanding its functionality and data types.

DOI 10.1101/2021.06.13.448171

database / resource

𝕏 PostBluesky