Lv41
540 积分 2021-08-12 加入
Detection of trait-associated structural variations using short-read sequencing
1个月前
已完结
DECoN: A Detection and Visualization Tool for Exonic Copy Number Variants
1个月前
已完结
[Relationship between heat stress protein 70 gene polymorphisms and the risk of acute mountain sickness]
1个月前
已关闭
GWAS shows the genetics behind cell-free DNA and highlights the importance of p.Arg206Cys in DNASE1L3 for non-invasive testing
1个月前
已完结
Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy
2个月前
已完结
Variant calling and benchmarking in an era of complete human genome sequences
4个月前
已完结
Additional diagnostic value of CNV‐seq over conventional karyotyping in prenatal diagnosis: A systematic review and meta‐analysis
5个月前
已完结
[Consensus on the application of clinical whole genome sequencing in the diagnosis of genetic diseases]
7个月前
已完结
Artificial Intelligence in Molecular Medicine
7个月前
已完结
The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing Data
8个月前
已完结
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