Lv1
100 积分 2024-07-25 加入
An Agentic System for Rare Disease Diagnosis with Traceable Reasoning
1个月前
已完结
Capturing sequence diversity in metagenomes with comprehensive and scalable probe design
1个月前
已完结
Genebe.net: Implementation and validation of an automatic ACMG variant pathogenicity criteria assignment
1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)
1个月前
已完结
Tutorial: annotation of animal genomes
1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)
3个月前
已完结
33. Customize your variant interpretation workflow with OpenCRAVAT
5个月前
已完结
PhenoBERT: A Combined Deep Learning Method for Automated Recognition of Human Phenotype Ontology
5个月前
已完结
DeepPGDB: A Novel Paradigm for AI-Guided Interactive Plant Genomic Database
6个月前
已完结
Laboratories of Autocracy: Landscape of Central–Local Dynamics in China’s Policy Universe
6个月前
已关闭