Match tier
Confirmed
Presence
Current · Arkansas
Last published
2021
Sources
OpenAlex · ORCID
Refreshed
2026-08-06
P
Penelope Duerken-Hughes
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Researcher
Unknown Researcher
2 h-index
2 pubs
147 cited
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Penelope Duerken-Hughes' research focuses on the development and application of reference standards for benchmarking cancer mutation detection using whole-genome sequencing. She has co-authored a publication in 2021 that established community reference samples, data, and call sets for this purpose. Duerken-Hughes collaborates with Weida Tong at the National Center for Toxicological Research, with whom she shares multiple publications. Her work contributes to improving the accuracy and reliability of genomic analyses in cancer research.
Metrics
- h-index: 2
- Publications: 2
- Citations: 147
Selected Publications
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Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing (2021)
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Establishing reference samples for detection of somatic mutations and germline variants with NGS technologies (2019)
Collaboration Network
Top Collaborators
Li Tai Fang
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Bin Zhu
National Cancer Institute (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Yongmei Zhao
Frederick National Laboratory for Cancer Research (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Wanqiu Chen
Loma Linda University (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Zhaowei Yang
Guangzhou Medical University (CN)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Liz Kerrigan
American Type Culture Collection (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Maryellen de Mars
American Type Culture Collection (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Charles Lu
AbbVie (United States) (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Kenneth B. Idler
AbbVie (United States) (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Howard J. Jacob
AbbVie (United States) (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Yuanting Zheng
Fudan University (CN)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Luyao Ren
State Key Laboratory of Genetic Engineering
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Ying Yu
Fudan University (CN)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Erich Jaeger
Fudan University (CN)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Gary P. Schroth
Illumina (United States) (US)
1 shared publication
- Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
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