Saturation-seq integrates single-cell saturation genome editing and RNA-seq to quantify NFE2L2 (NRF2) variant effects
Magdalena E Strauß, Andrew J. Waters, Holly Roberston, Timothy Brendler-Spaeth, Aleksander M. Gontarczyk, Prashant Gupta, Shikha Kataria, Daniel P. Gitterman, Tumisang Ntereke, Leah Wells, Jamie Billington, Andrew Roger Bassett, Sarah Cooper, D. Adams
Saturation-seq combines genome editing and single-cell RNA-seq to quantify variant effects on NFE2L2, accurately distinguishing pathogenic from benign variants.
bioRxiv · Jul 4, 2026 · PreprintGenomics