Author

Kyle Davis

BioNano Genomics (United States)ORCID 0000-0003-1874-9741Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Kyle Davis1 paper · Complete Genomics (United States)

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amanda Thomas‐WilsoniD· 1 shared Ana S.A. CoheniD· 1 shared Anna SzutoiD· 1 shared Brittany C. ThomasiD· 1 shared Carol SaundersiD· 1 shared Christian R. MarshalliD· 1 shared Christian S. Neckelmann· 1 shared Christina DiVincenzo· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amanda Thomas‐WilsonORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedJul 30, 2023

The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change

Heidi L. Rehm, Joseph T. Alaimo, Swaroop Aradhya…·Stephen Francis Kingsmore

The paper analyzes VUS rates in genetic testing and finds lower rates in exome/genome sequencing compared to multi-gene panels, suggesting improvements in variant reporting practices.

138 citationstop 1%

whole-exome sequencingwhole-genome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintFeb 4, 2021

NeuroSCORE: A Genome-wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System

Kyle Davis, Colleen G. Bilancia, Megan M. Martin…·Moises A. Serrano

NeuroSCORE scores 19,598 genes based on five CNS-related metrics, identifying 1,580 high-scoring genes significantly associated with CNS phenotypes.

DOI 10.1101/2021.02.04.429640

humanwhole-genome sequencing

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