Author

Paul E. Lund

10X Genomics (United States)ORCID 0000-0003-0496-1434Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Organism:human· 1 Assay:scRNA-seq· 1 Research Focus:trajectory inference· 1

Frequent Co-Authors

Andrew S. Kohlway· 2 shared Alexander SwarbrickiD· 1 shared Alissa GreenwaldiD· 1 shared Andrés F. VallejoiD· 1 shared Anna ElziD· 1 shared Austin VarelaiD· 1 shared Azi Hadadianpour· 1 shared Beata KiedikiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenomics

Andrew S. Kohlway

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintJul 3, 2026

Scalable genotyping in fixed transcriptomes resolves clonal heterogeneity via single-cell sequencing

Sydney B. Blattman, Nabih Maslah, Austin Varela…·Caleb A. Lareau

GIFT enables high-accuracy genotyping in single cells, revealing mutation-dependent hematopoietic responses in MPN patients.

DOI 10.64898/2026.04.11.717967

𝕏 PostBluesky

Molecular BiologybioRxivPreprintDec 7, 2023

snPATHO-seq: unlocking the pathology archives

Taopeng Wang, Kate Harvey, Javier Escudero Morlanes…·Luciano Gastón Martelotto

This study introduces a method to generate high-quality single-nucleus transcriptomic data from FFPE samples using recent single-cell genomic technology.

4 citations

bulk RNA-seqexperimental assay

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