Lv3
250 积分 2025-02-27 加入
Scalable homology detection with ERAST
18小时前
已完结
Bioinformatics and artificial intelligence in genomic data analysis: current advances and future directions
6天前
已完结
A comprehensive and bias-free evaluation of genomic variant clinical interpretation tools
6天前
已关闭
Low‐Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuses
8天前
已完结
HumanBase: an interactive AI platform for human biology
10天前
已完结
ISUOG Practice Guidelines: point‐of‐care ultrasound in obstetrics and gynecology
2个月前
已完结
Additional diagnostic yield through the analysis of short tandem repeats based on exome sequencing data
2个月前
已完结
Resolving structural variations missed by short-read sequencing uncovers their pathogenicity
3个月前
已关闭
Somatic mutations at scale
3个月前
已完结
Sourmash Branchwater Enables Lightweight Petabyte-Scale Sequence Search
3个月前
已完结
[Unexpected discovery of a fetus with DMD gene deletion using single nucleotide polymorphism array]
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