cadd-snv¶
appears in¶
original citations¶
Schubach M, Maass T, Nazaretyan L, Röner S, Kircher M. CADD v1.7: Using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions. Nucleic Acids Res. 2024 Jan 5. doi: 10.1093/nar/gkad989. PubMed PMID: 38183205.
Rentzsch P, Witten D, Cooper GM, Shendure J, Kircher M. CADD: predicting the deleteriousness of variants throughout the human genome. Nucleic Acids Res. 2018 Oct 29. doi: 10.1093/nar/gky1016. PubMed PMID: 30371827.