Large structural variants in KOLF2.1J are unlikely to compromise neurological disease modelling
M. Ryan, J. A. McDonough, M. E. Ward, M. R. Cookson, W. C. Skarnes, F. T. Merkle
The paper evaluates CNVs in a hiPSC line and concludes that their potential impact on neurological disease modelling is outweighed by the line's benefits.
bioRxiv · Jan 29, 2024 · PreprintCell Biology