Author

Paul D. Blischak

The Ohio State UniversityORCID 0000-0001-9177-8958Unclaimed 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 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Assay:DNA methylation· 1 Assay:imaging· 1 Organism:plant (other)· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Andrea D. WolfeiD· 2 shared Brandin Grindstaff· 1 shared David C. TankiD· 1 shared Diego F. Morales‐BrionesiD· 1 shared J. Chris PiresiD· 1 shared Jens C. Johnson· 1 shared Laura Salter KubatkoiD· 1 shared Makenzie E. MabryiD· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersBioinformatics

Andrea D. WolfeORCID

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3 papers

Recent·Most cited

BioinformaticsApplications in Plant SciencesPeer-reviewedAug 1, 2019

Affordable Remote Monitoring of Plant Growth and Facilities using Raspberry Pi Computers

Brandin Grindstaff, Makenzie E. Mabry, Paul D. Blischak…·J. Chris Pires

The paper develops a low-cost system using Raspberry Pi computers to monitor growth chamber conditions, enabling automated data logging and remote alerts.

32 citations

plant (other)imaging

𝕏 PostBluesky

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

𝕏 PostBluesky

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