Author

Skylar Martin

University of Colorado Boulder

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Ryan M. LayeriD· 2 shared Adam M. PhillippyiD· 1 shared Alaina ShumateiD· 1 shared Alisa Gaskell· 1 shared Arang RhieiD· 1 shared Bailey K. FosdickiD· 1 shared Benedict PateniD· 1 shared Chen-Shan ChiniD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersBioinformatics

Ryan M. LayerORCID

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Author profile →

2 papers

Recent·Most cited

Hypothesis Generation For Rare and Undiagnosed Diseases Through Clustering and Classifying Time-Versioned Biological Ontologies

Michael S. Bradshaw, Connor P. Gibbs, Skylar Martin, Taylor Firman, Alisa Gaskell, Bailey K. Fosdick, Ryan M. Layer

This paper identifies potential gene-to-phenotype connections for undiagnosed diseases by clustering time-versioned biological ontologies and analyzing network data.

PLoS ONE · Dec 26, 2024Peer-reviewedBioinformatics

A complete reference genome improves analysis of human genetic variation

Sergey S. Aganezov, Stephanie M. Yan, Daniela C. Soto, Melanie Kirsche, Samantha Zarate, Pavel Avdeyev, Dylan J. Taylor, Kishwar Shafin, Alaina Shumate, Chunlin Xiao, Justin Wagner, Jennifer McDaniel, Nathan D. Olson, Michael E.G. Sauria, Mitchell Robert Vollger, , Michael C. Schatz

The T2T-CHM13 reference genome improves read mapping and variant calling across diverse samples, reducing false positives and enabling novel variant discovery.

Science · Mar 31, 2022Peer-reviewedGenomics