Match tier
Confirmed
Presence
Current · Arkansas
Last published
2022
Sources
OpenAlex · ORCID
Refreshed
2026-10-05
J
Joe Meehan
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Computer Scientist
Also affiliated: United States Food and Drug Administration (2013–2022); Western Washington University (2005–2006)
11 h-index
36 pubs
2,088 cited
Research Areas
Biomedical Subjects
Links
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: 11
- Publications: 36
- Citations: 2,088
Positions
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Computer Scientist publications 1991–2022National Center for Toxicological Research Bioinformatics and Biostatistics ORCID
Selected Publications
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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)
Collaboration Network
Top Collaborators
Andreas Scherer
University of Helsinki (FI)
16 shared publications
- The concordance between RNA-seq and microarray data depends on chemical treatment and transcript abundance
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 16 shared publications
Baitang Ning
National Center for Toxicological Research
16 shared publications
In database
- An investigation of biomarkers derived from legacy microarray data for their utility in the RNA-seq era
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 16 shared publications
Bohu Pan
National Center for Toxicological Research
15 shared publications
In database
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Luyao Ren
Fudan University (CN)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Vitor Onuchic
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Meijian Guan
SAS Institute (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Rebecca Kusko
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Steve Bruinsma
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Len Trigg
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Christine Glidewell-Kenney
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Chunlin Xiao
National Center for Biotechnology Information (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Eric Donaldson
United States Food and Drug Administration (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Fritz J. Sedlazeck
Baylor College of Medicine (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Gary P. Schroth
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Gökhan Yavaş
National Center for Toxicological Research (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
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