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History
- November 13, 2021.
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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
Author Information
- Beau R. Webber1,2,3,*,
- Matthew J. Johnson1,2,3,*,
- Nicholas J. Slipek1,2,3,
- Walker S. Lahr1,2,3,
- Anthony P. DeFeo1,2,3,
- Joseph G. Skeate1,2,3,
- Xiaohong Qiu1,2,3,
- Blaine Rathmann1,2,3,
- Miechaleen D. Diers1,2,3,
- Bryce Wick1,2,3,
- Tom Henley4,
- Modassir Choudhry4,
- R. Scott McIvor3,5 and
- Branden S. Moriarity1,2,3,*
- 1Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA
- 2Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA
- 3Center for Genome Engineering, University of Minnesota, Minneapolis, MN, USA
- 4Intima Bioscience, New York, USA
- 5Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN, USA
- ↵*Corresponding author; email: mori0164{at}umn.edu
↵* These authors contributed equally.
Posted November 13, 2021.
Homology mediated end joining enables efficient non-viral targeted integration of large DNA templates in primary human T cells
