Joe Meehan Source Confirmed
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Computer Scientist
National Center for Toxicological Research
faculty
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Biography and Research Information
OverviewAI-generated summary
Joe Meehan's research investigates the reproducibility of inherited variants identified through short-read whole genome sequencing. His work focuses on computational methods to ensure the accuracy and reliability of genetic data analysis, particularly within the context of toxicological research. Meehan has a publication record of 42 articles, with 3,113 citations and an h-index of 14. He has a history of collaboration with researchers at the National Center for Toxicological Research, including Bohu Pan and Weigong Ge, with whom he has co-authored 15 publications.
Metrics
- h-index: 14
- Publications: 42
- Citations: 3,113
Selected Publications
- Additional file 3 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 13 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 5 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 15 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 10 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 9 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 11 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 1 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 6 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 12 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022) DOI
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