Author

Quan Peng

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:snRNA-seq· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Bardia Nezami· 1 shared Beth O. Van Emburgh· 1 shared Chang XuiD· 1 shared Dongsan KimiD· 1 shared Jaldhir Trivedi· 1 shared Javier Redding‐OchoaiD· 1 shared Jinhee ParkiD· 1 shared John DiCarlo· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenomics

Bardia Nezami

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2 papers

Recent·Most cited

Dissecting the molecular landscape of Parkinson's disease and Parkinson's disease dementia using highly efficient snRNA-seq (HIF-snRNA-seq)

Sung-Ung Kang, Jinhee Park, Shinwon Ha, Dongsan Kim, Olga Pletniková, Javier Redding‐Ochoa, Juan Carlos Troncoso, Quan Peng, Beth O. Van Emburgh, Jaldhir Trivedi, Saurav Brahmachari, Bardia Nezami, Valina Lynn Dawson, Ted M. Dawson

This study uses HiF-snRNA-seq to analyze the cingulate cortex in Parkinson's disease and Parkinson's disease dementia, identifying cell-type-specific gene expression changes and disease-stage-related pathways.

bioRxiv · Mar 1, 2025 · PreprintGenomics

smCounter2: an accurate low-frequency variant caller for targeted sequencing data with unique molecular identifiers

Chang Xu, Xiujing Gu, Raghavendra Padmanabhan, Zhong Wu, Quan Peng, John DiCarlo, Yexun Wang

smCounter2 improves variant calling for targeted sequencing data by reducing technical errors and enhancing accuracy, particularly in non-coding regions.

Bioinformatics · Sep 5, 2018Peer-reviewedBioinformatics