Lv719
3310 积分 2022-03-09 加入
Population survey of repeat expansion mutations
12天前
已完结
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon
30天前
已完结
MethSCAn: accurate exploratory analysis of single-cell methylomes
3个月前
已完结
Unveiling microbial diversity: harnessing long-read sequencing technology
3个月前
已完结
Improving estimates of loss-of-function constraint for short genes
3个月前
已完结
GALAXY Workflow for Bacterial Next‐Generation Sequencing De Novo Assembly and Annotation
4个月前
已完结
Improving transparency of computational tools for variant effect prediction
4个月前
已完结
Mining the diagnosis of rare disease with limited resources
4个月前
已完结
Sequencing-based analysis of microbiomes
4个月前
已完结
Scanorama: integrating large and diverse single-cell transcriptomic datasets
5个月前
已完结
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