Author

Kiran Narta

University of CalgaryORCID 0000-0002-0645-6581Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 2 Research Focus:drug response / drug discovery· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Approach:experimental assay· 1

Frequent Co-Authors

A. Sorana MorrissyiD· 2 shared Aayush GuptaiD· 1 shared Aly O. AbdelkareemiD· 1 shared Archana Kumari SinghiD· 1 shared Arijit MukhopadhyayiD· 1 shared Athish Marutharaj· 1 shared Courtney F. Hall· 1 shared Debasis DashiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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2 shared papersGenomics

A. Sorana MorrissyORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Compound Delivery of eVLPs Enhances Prime Editing for Targeted Genome Engineering and High-Throughput Screening

Jethro Langley, Lou Baudrier, J.E. Curry, Kiran Narta, Hayley M. Todesco, Kyle G. Potts, A. Sorana Morrissy, Douglas J. Mahoney, Pierre Billon

This paper introduces PRIME-VLP, a delivery strategy that enhances prime editing efficiency for genome engineering and high-throughput screening using eVLPs.

Cell Genomics · Jul 14, 2026Peer-reviewedGenomics

XenoSignal: Investigating Intra- and Inter-Species Ligand-Receptor Interactions Using AlphaFold3

Aly O. Abdelkareem, Courtney F. Hall, Athish Marutharaj, Kiran Narta, Theodore B. Verhey, A. Sorana Morrissy

XenoSignal assesses ligand-receptor interactions across species using AlphaFold3 predictions to improve understanding of tumor-microenvironment crosstalk in xenograft models.

bioRxiv · Aug 13, 2025 · PreprintBioinformatics

Whole exome-sequencing of vitiligo lesions indicate lower burden of somatic variations: implications in risk for non-melanoma skin cancers

Iti Gupta, Shambhavi Shankrit, Kiran Narta, Madeeha Ghazi, Ritika Grover, Rajesh Pandey, Hemanta Kumar Kar, Shruti M. Menon, Aayush Gupta, Vamsi Krishna Yenamandra, Archana Kumari Singh, Mitali Mukerji, Arijit Mukhopadhyay, Rajni Rani, Rajesh S. Gokhale, , Vivek T. Natarajan

The paper uses whole exome sequencing to show lower somatic mutation burden in vitiligo lesions, linked to reduced non-melanoma skin cancer risk through enhanced DNA repair.

Journal of Investigative Dermatology · Dec 16, 2022Peer-reviewedGenomics