Match tier Confirmed
Presence Current · Arkansas
Last published 2022
Sources OpenAlex · ORCID
Refreshed 2026-08-15

Joe Meehan

Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.

Computer Scientist

Also affiliated: Alaska Department of Fish and Game (2005); NOAA National Marine Fisheries Service (2002); United States Food and Drug Administration (2013–2022); Office of Science (2002); Western Washington University (2005–2006)

Faculty Researcher

10 h-index 37 pubs 1,040 cited

  • Humans
  • Polymorphism, Single Nucleotide
  • Sequence Analysis, RNA
  • Genome, Human
  • Oligonucleotide Array Sequence Analysis
  • Algorithms
  • High-Throughput Nucleotide Sequencing
  • Animals
  • Rats
  • Genetic Markers
  • Computational Biology
  • Reproducibility of Results
  • Deep Learning
  • Pharmaceutical Preparations
  • Salmonella

Biography and Research Information

OverviewAI-generated summary

Joe Meehan's research focuses on the computational analysis of genetic data, particularly concerning the reproducibility and detection of inherited variants in whole genome sequencing. His work investigates algorithms and computational biology techniques applied to sequence analysis. Meehan has published research examining the accuracy of inherited variant detection methods, with a significant portion of his recent publications detailing supplementary files related to this topic. His collaborations include extensive work with Bohu Pan and Weigong Ge at the National Center for Toxicological Research, each sharing 15 publications. He also collaborates with Wen Zou (6 shared publications) and Wenjing Guo (1 shared publication). Meehan's scholarly contributions are reflected in his h-index of 10 and over 1,000 total citations from 37 publications.

Metrics

  • h-index: 10
  • Publications: 37
  • Citations: 1,040

Selected Publications

  • Additional file 3 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 13 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 5 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 15 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 10 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 9 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 11 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 1 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 6 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 12 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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  • Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
    Genome biology 56 citations DOI OpenAlex

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Collaboration Network

27 Collaborators 12 Institutions 3 Countries

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