Lv4
560 积分 2023-03-31 加入
Assessing the Utility of Large Language Models for Phenotype-Driven Gene Prioritization in Rare Genetic Disorder Diagnosis
28天前
已完结
Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations
1个月前
已完结
Long-read sequencing solves complex structure of CYP21A2 in a large 21-hydroxylase deficiency cohort
8个月前
已完结
Guidance for estimating penetrance of monogenic disease-causing variants in population cohorts
8个月前
已完结
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment
1年前
已完结
Accurate proteome-wide missense variant effect prediction with AlphaMissense
1年前
已完结
Pharmacogenetics of anxiety and depression in Alzheimer's disease
1年前
已完结
Role of Pharmacogenomics in Individualizing Treatment for Alzheimer’s Disease
1年前
已完结
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