Lv3
320 积分 2025-02-27 加入
allofus: an R package to facilitate use of the All of Us Researcher Workbench
2个月前
已完结
DRAGEN optimizes genomic variant detection
2个月前
已完结
Scalable homology detection with ERAST
2个月前
已完结
Bioinformatics and artificial intelligence in genomic data analysis: current advances and future directions
3个月前
已完结
A comprehensive and bias-free evaluation of genomic variant clinical interpretation tools
3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
3个月前
已完结
HumanBase: an interactive AI platform for human biology
3个月前
已完结
ISUOG Practice Guidelines: point‐of‐care ultrasound in obstetrics and gynecology
5个月前
已完结
Additional diagnostic yield through the analysis of short tandem repeats based on exome sequencing data
5个月前
已完结
Resolving structural variations missed by short-read sequencing uncovers their pathogenicity
6个月前
已关闭
[Unexpected discovery of a fetus with DMD gene deletion using single nucleotide polymorphism array]
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