“…Pathogenic synonymous mutations SilVA (Buske et al, 2013) Random forest DDIG-SN (Livingstone et al, 2017) Support vector machine regSNPs-splicing (Zhang et al, 2017a) Random forest Syntool (Zhang et al, 2017b) -TraP (Gelfman et al, 2017) Random forest Genome sequencing CADD (Kircher et al, 2014) Support vector machine MutationTaster2 (Cooper, 2014) Naive Bayes Mut-Pred (Li et al, 2009) Random forest PolyPhen-2 (Adzhubei et al, 2010) Naive Bayes PON-P2 (Niroula et al, 2015) Random forest VEST (Carter et al, 2013) Random forest Deep mining of structural variation information DeepBind (Alipanahi et al, 2015) deep learning DeepVariant (Angermueller et al, 2017) deep neural networks DeepCpG (Poplin et al, 2018) deep 2019; Liu et al, 2020a;Jin et al, 2021;Yin et al, 2021). The published methods include CADD (Kircher et al, 2014), MutationTaster2 (Cooper, 2014),Mut-Pred (Li et al, 2009),PolyPhen-2 (Adzhubei et al, 2010),PON-P2 (Niroula et al, 2015) and VEST (Carter et al, 2013).…”