Joe Meehan Data-verified

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

Computer Scientist

Last publication 2022 Last refreshed 2026-04-25

faculty

10 h-index 37 pubs 1,032 cited

Biography and Research Information

OverviewAI-generated summary

Joe Meehan's research focuses on the computational analysis of genetic data, particularly concerning the reproducibility of variant detection in whole-genome sequencing. His work has explored the assessment of inherited variants using short-read sequencing technologies. Meehan has a significant publication record, with 42 total publications and over 3,100 citations, reflecting a h-index of 14. He has collaborated extensively with researchers at the National Center for Toxicological Research, including Bohu Pan and Weigong Ge, with whom he shares 15 co-authored publications. His recent publications, primarily from 2022, highlight his continued activity in the field of bioinformatics and sequence analysis.

Metrics

  • h-index: 10
  • Publications: 37
  • Citations: 1,032

Selected Publications

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

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Collaboration Network

27 Collaborators 12 Institutions 3 Countries

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