Author

Andrea D. Wolfe

The Ohio State UniversityORCID 0000-0002-2697-663XUnclaimed 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 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Paul D. BlischakiD· 2 shared David C. TankiD· 1 shared Diego F. Morales‐BrionesiD· 1 shared Jens C. Johnson· 1 shared Laura Salter KubatkoiD· 1 shared Maribeth LatvisiD· 1 shared Verónica S. Di StilioiD· 1 shared

Activity by Year

2017-2018 · peak 1/yr

Co-Author Collaboration Network

7 top collaborators · 16 mutual co-author links

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2 shared papersBioinformatics

Paul D. BlischakORCID

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2 papers

Recent·Most cited

BioinformaticsApplications in Plant SciencesPeer-reviewedJun 1, 2018

Fluidigm2PURC: automated processing and haplotype inference for double-barcoded PCR amplicons

Paul D. Blischak, Maribeth Latvis, Diego F. Morales‐Briones…·David C. Tank

Fluidigm2PURC automates processing and haplotype inference for double-barcoded PCR amplicons, enabling analysis of diploid, polyploid, and unknown ploidy samples.

16 citations

DNA methylationwhole-genome sequencing

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BioinformaticsBioinformaticsPeer-reviewedSep 15, 2017

SNP genotyping and parameter estimation in polyploids using low-coverage sequencing data

Paul D. Blischak, Laura Salter Kubatko, Andrea D. Wolfe

The paper develops models for genotyping and parameter estimation in polyploids using low-coverage sequencing data and shows they reduce estimation error compared to existing methods.

74 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky