Lv31
360 积分 2025-02-27 加入
AAVC: An automated framework for high-accuracy ACMG-based variant classification
10天前
已完结
AI-CURA, an automated LLM workflow for high-accuracy genetic variant classification
10天前
已完结
Annotating genomes at increased scale and resolution
24天前
已完结
Harmonizing standards and resources for the medical genome
1个月前
已完结
allofus: an R package to facilitate use of the All of Us Researcher Workbench
4个月前
已完结
DRAGEN optimizes genomic variant detection
4个月前
已完结
Scalable homology detection with ERAST
4个月前
已完结
Bioinformatics and artificial intelligence in genomic data analysis: current advances and future directions
4个月前
已完结
A comprehensive and bias-free evaluation of genomic variant clinical interpretation tools
4个月前
已关闭
Low‐Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuses
4个月前
已完结
[Unexpected discovery of a fetus with DMD gene deletion using single nucleotide polymorphism array]
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