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48 积分 2025-10-29 加入
A spectral approach integrating functional genomic annotations for coding and noncoding variants
1天前
待确认
Adam: A Method for Stochastic Optimization
4天前
已完结
The SynMall resource for characterizing the functional impact of synonymous variation
7天前
已完结
dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs
18天前
已完结
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
1个月前
已完结
Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications
1个月前
已完结
S-CAP extends pathogenicity prediction to genetic variants that affect RNA splicing
2个月前
已完结
Predicting expression-altering promoter mutations with deep learning
3个月前
已完结
A disease-specific language model for variant pathogenicity in cardiac and regulatory genomics
3个月前
已完结
Transfer learning enables predictions in network biology
3个月前
已完结
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