Lv2
110 积分 2023-02-02 加入
Inferring compound heterozygosity from large-scale exome sequencing data
1年前
已完结
Drug discovery companies are customizing ChatGPT: here’s how
1年前
已完结
Disease variant prediction with deep generative models of evolutionary data
1年前
已完结
Curated variation benchmarks for challenging medically relevant autosomal genes
1年前
已完结
Principles and methods for transferring polygenic risk scores across global populations
2年前
已完结
Octopus: Genotyping and Haplotyping in Diverse Experimental Designs
2年前
已完结
Evaluation of an automated genome interpretation model for rare disease routinely used in a clinical genetic laboratory
2年前
已完结
Phen2Disease: a phenotype-driven model for disease and gene prioritization by bidirectional maximum matching semantic similarities
2年前
已完结
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