Lv21
104 积分 2023-02-13 加入
Benchmarking large language models for replication of guideline-based PGx recommendations
1小时前
求助中
HCSeeker: A Classification Tool for Human Genetic Variant Hot and Cold Spots Designed for PM1 and Benign Criteria in the ACMG-AMP Guideline
29天前
已完结
Genebe.net: Implementation and validation of an automatic ACMG variant pathogenicity criteria assignment
1个月前
已完结
[Expert consensus on the standardized application of whole exome sequencing technology in diagnosis of genetic disorders]
1个月前
已完结
AI-MARRVEL — A Knowledge-Driven AI System for Diagnosing Mendelian Disorders
2个月前
已完结
Research on Cloud Infrastructure for Large-Scale Parallel Computing in Genetic Disease
2个月前
已关闭
AutoPVS1: An automatic classification tool for PVS1 interpretation of null variants
2个月前
已完结
[Expert consensus on the clinical application strategy of NIPT2.0, a new-generation non-invasive prenatal screening technology]
2个月前
已完结
[Expert consensus on the clinical application strategy of NIPT2.0, a new-generation non-invasive prenatal screening technology]
3个月前
已完结
In vivo CAR T cell generation to treat cancer and autoimmune disease
4个月前
已完结
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