Associated Papers
Benchmarking of SpCas9 variants enables deeper base editor screens of BRCA1 and BCL2.
Sangree AK et al.
Nature Communications, 2022
35288574 (PubMed )
Supplement: 41467_2022_28884_MOESM11_ESM.xlsx › NG-ABE_Library_Annotation
Consequences of genetic variants in miRNA genes.
Machowska M et al.
Computational and Structural Biotechnology Journal, 2022
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