Lv2
118 积分 2024-07-25 加入
AI-CURA, an automated LLM workflow for high-accuracy genetic variant classification
3个月前
已完结
AI-CURA, an automated LLM workflow for high-accuracy genetic variant classification
3个月前
已完结
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data
4个月前
已完结
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data
4个月前
已完结
An Agentic System for Rare Disease Diagnosis with Traceable Reasoning
7个月前
已完结
Capturing sequence diversity in metagenomes with comprehensive and scalable probe design
7个月前
已完结
Genebe.net: Implementation and validation of an automatic ACMG variant pathogenicity criteria assignment
7个月前
已完结
The first Japanese cases of familial hypercholesterolemia due to a known pathogenic APOB gene variant, c.10580 G>A: p.(Arg3527Gln)
8个月前
已完结
Tutorial: annotation of animal genomes
8个月前
已完结
原发性醛固酮增多症诊断治疗的专家共识(2024版)
10个月前
已完结
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