Author

Daniel J. Laverty

Harvard UniversityORCID 0000-0003-4529-2302Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Assay:CRISPR screen· 1 Research Focus:drug response / drug discovery· 1 Assay:long-read sequencing· 1 Research Focus:perturbation response prediction· 1

Frequent Co-Authors

Zachary David NageliD· 2 shared Abolfazl Salehi MoghaddamiD· 1 shared Alexander Arteaga· 1 shared Ana Cheong· 1 shared Andrew C. Puncheon· 1 shared Anthony J. DavisiD· 1 shared Benjamin P.C. CheniD· 1 shared Gareth J Williams· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersMolecular Biology

Zachary David NagelORCID

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3 papers

Recent·Most cited

BioengineeringbioRxivPreprintMay 30, 2026

Integrative Multiomic Analysis Reveals How Non-Viral Delivery System Selection Shapes CRISPR Gene Editing Outcomes in Stem Cells.

Joshua P. Graham, Alexander Arteaga, Abolfazl Salehi Moghaddam…·Tomas Gonzalez‐Fernandez

This study compares non-viral CRISPR delivery methods in stem cells, finding that lipid-based delivery offers high efficiency but risks genomic instability, while CPPs reduce side effects at lower efficiency.

DOI 10.64898/2026.05.29.728905

humanCRISPR screen

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Molecular BiologyJournal of Molecular BiologyPeer-reviewedApr 16, 2026

MSIanalyzer: Targeted Nanopore Sequencing Enables Single Nucleotide Resolution Analysis of Microsatellite Instability Diversity

Ting Zhai, Ana Cheong, Daniel J. Laverty, Zachary David Nagel

MSIanalyzer uses targeted nanopore sequencing to analyze microsatellite instability at single-nucleotide resolution, revealing distinct repeat profiles and allelic diversity in cancer cell lines.

DOI 10.1016/j.jmb.2026.169812

humanlong-read sequencing

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Molecular BiologyNucleic Acids ResearchPeer-reviewedMay 31, 2023

ATM phosphorylates the FATC domain of DNA-PKcs at threonine 4102 to promote non-homologous end joining

Huiming Lu, Qin Zhang, Daniel J. Laverty…·Anthony J. Davis

This study identifies ATM phosphorylation of DNA-PKcs at T4102 as critical for stabilizing NHEJ machinery and promoting DSB repair.

19 citations

experimental assay

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